Kumkuma Kesara: The Saffron Gold of Spices

Introduction

Kumkuma Kesara is a triploid herbaceous plant i.e., the most expensive spice in the world. Kumkuma Kesara botanically known as Crocus sativus belongs to the Iridaceae family and was originally cultivated in the East and Middle East. Saffron i.e., Kumkuma Kesara not only has medicinal properties, but it has various culinary uses due to which it is famous as the gold of spices. Kumkuma Kesara is rich in various active principles like crocin, 1, 2, 3, 4, crocetin, crocins, esters of crocetin, picrocrocin, crosatosides A and B which not only give its taste and aroma but made it powerful anti-inflammatory and antioxidant herb. Recent research revealed that it exhibits various other pharmacological properties like an anti-tumor and cardioprotective activity. Along with this Kumkuma kesara is a promising agent in treating various neurological disorders, digestive system, and reproductive system-related disorders. It plays a great role in treating dysmenorrhea, delayed labor, delayed periods, etc. Kumkuma Kesara also exhibits various properties which make it a boon for skin disorders like Nyacha, Vyanga (discoloration of the face), and scars, and it also helps in imparting a glowing complexion.

Basonym of Kumkum Keasara

शब्द: स्तूयते ।

Kumkum is very sacred and all worship.

Synonyms of Kumkum Kesara

  • According to habitat

काश्मीरम- कश्मीरे भवम्‌। 

Grows in Kashmir region.

बाह्लिकं – बाह्लिक देशे उप्लभ्य्मानं।

Found in Bahlika Desha (Punjab province of Pakistan).

  • According to morphology

अग्नि शिखम – अग्रेशिखेव केशरो अस्य 

Kesara resembles a fire flame.

कुसुमोदभवम्‌- कुसुमादुद्भवो अस्य 

Kesara (stigma) which is a useful part and obtained from flowers.

  • According to properties and actions

रक्तं – रक्तवर्णम्‌ 

Kumkuma is red in color.

पीतकम– पीतवर्ण जनयति 

Imparts yellow color if mixed with water.

वर्ण्यम– वर्णाय हितम्‌ 

Kumkuma imparts color.

कुसुम्भ– कुसुम्भवर्णम्‌ 

Imparts yellow color like that of Kusumbha (Carthamus tinctorius).

तीव्रम– तीक्ष्ण गन्धि।

Kumkuma has a very potent odour.

पिशुनम्‌- सूच्यते गन्धेन ।

Has a strong odour.

वरम् – वीर्यतेकामयतेइति।

Liked by everybody because of its bright and attractive color.

Regional Names of Kumkum Kesara

  • Saffron (English)
  • Kesar (Hindi)
  • Kumkuma Kesara (Kannada)
  • Kunkumappu (Malayalam)
  • Kecara (Marathi)
  • Jafran Kumkuma (Bengali)
  • Kesar (Gujrati)
  • Kunkumappu (Tamil)
  • Kunkum- pubba (Telugu)
  • Jaffran (Arabic)
  • Karakimas (Persian)

Botanical Name

Crocus sativus Linn.

Crocus – Name adopted from theophrastus, sativus cultivated.

Family

Iridaceae (Kesara Kula)

Ayurveda Reference for Kumkum Kesara (Crocus sativus Linn.)

Scientific Classification of Kumkum Kesara

KingdomPlantae
Class Monocotyledons 
Series Epigynae
Family Iridaceae
GenusCrocus 
Species Sativus

Classification of Kumkuma – As Per Charaka and Sushruta

Charaka: Shonit Sthapana Mahakashaya

Sushruta: Eladi Gana

Kumkum Kesara’s Description in Brihtrayi as Kumkuma

Besides this which may be called Trina (grass) Kunkuma, there is also a Vriksa (tree) Kunkuma in which the basal part of the stem is covered by a layer of the saffron-colored part which is entirely a fungal tissue. This small tree is identified as Euonymus tingens Wall. is widely known by the name of Kunkuma or other similar names. It appears that as regards the uses of real Kunkuma in eye diseases, this can serve as a substitute. Sushruta has also used it under the name of Bimbilota or Bhillota.

Charaka Shusruta Vagbhata (Ashtang Hridya)
C. S. Chi. 23/ 53, 77, 189S. S. Su. 28/ 13A. H. Su. 3/ 11, 15, 20
C. S. Chi. 26/ 51S. S. Su. 38/ 24A. H. Su. 15/ 43
C. S. Chi. 28/ 151, 160S. S. Su. 46/ 287A. H. Su. 21/ 15
C. S. Chi. 29/ 112S. S. Chi. 4/ 24A. H. Chi. 1/ 137
S. S. Ka. 6/ 22A. H. Chi. 7/ 18
S. S. Ka. 7/ 33A. H. Chi. 11/ 7
S. S. Ka. 8/ 49A. H. Chi. 21/ 77
S. S. U. 12/ 13A. H. U. 12/ 13
S. S. U. 39/ 244, 274A. H. U. 39/ 244, 274
S. S. U. 55/ 25A. H. U. 55/ 25
S. S. U. 58/ 31A. H. U. 58/ 31

Kumkum Kesara’s Description in Brihtrayi as Kashmiraja

Ashtanga Hridya: A. H. U. 37/ 44

Kumkum Kesara’s Description in Brihtrayi as Ibha

Here Ibha Kesara has to be split up into Ibha and Kesara

Sushruta Samhita: S. S. Chi. 38/ 51

Kumkum Kesara’s Description in Brihtrayi as Kesara, Kesarahvaya, Keshara

Kesara has, in most cases, been treated as a synonym of Nagakesara, where preceded by Padma or its synonyms, as only Padmakesara or as Padma and Kesara both. Dalhana, has, however, interpreted it also as another name for Bakula. It appears that Kesara has never been used in the texts as a synonym for Kasmiraja Kesara.

Charaka Shusruta Vagbhata (Ashtang Hridya)
C. S. Su. 5/ 17S. S. Chi. 9/ 13, 32A. H. Su. 6/ 160
C. S. Vi. 8/ 151S. S. Chi. 11/ 9A. H. Sa. 2/ 3
C. S. Chi. 1. 1/ 67S. S. Chi. 37/ 30A. H. Chi. 1/ 56, 99
C. S. Chi. 2. 1/ 30S. S. Chi. 38/ 51A. H. Chi. 3/ 76, 98
C. S. Chi. 4/ 94S. S. Ka. 6/ 8A. H. Chi. 5/ 71
C. S. Chi. 5/ 157S. S. U. 39/ 227, 230A. H. Chi. 8/ 115, 117, 128
C. S. Chi. 6/ 30, 41S. S. U. 40/ 74A. H. Chi. 16/ 38
C. S. Chi. 7/ 129S. S. U. 47/ 46, 61A. H. Chi. 19/ 88
C. S. Chi. 8/ 77, 82, 83S. S. U. 62/ 23A. H. Ka. 2/ 62
C. S. Chi. 9/ 42A. H. U. 28/ 35
C. S. Chi. 11/ 18A. H. U. 32/ 31
C. S. Chi. 14/ 164, 197, 199, 210 (Ambhoja Kesara in Vagbhata)A. H. U. 35/ 23, 24
C. S. Chi. 15/ 164A. H. U. 36/ 83
C. S. Chi. 16/ 120A. H. U. 37/ 71, 83
C. S. Chi. 21/ 96A. H. U. 40/ 20
C. S. Chi. 23/ 95, 192
C. S. Chi. 27/ 42
C. S. Chi. 29/ 106, 111
C. S. Ka. 7/ 31, 73
C. S. Si. 3/ 48
C. S. Si. 12/ 54

Kumkum Kesara’s Description in Brihtrayi as Gandha Aushadha

Gandha, Sarvagandha, and Gandhausadha are group names of aromatic drugs usually included in the Eladi Gana (S. S. Su. 38. 21). Sometimes Aguru, Kankkola, Karpura, Kunkuma, Caturjataka, and Lavanga only are taken as Sarvagandha substances. By Gandassch Agaru Patradya is meant all aromatic substances from Aguru to Devadaru except Kustha and Tagara mentioned in C. S. Ci. 3. 266. 

Charaka Samhita: C. S. Su. 3/ 18, C. S. Su. 5/ 23, C. S. Su. 14/ 35, C. S. Sa. 8/ 79, C. S. Chi. 8/ 117, C. S. Chi. 12/ 65, C. S. Chi. 26/ 181, C. S. Chi. 27/ 52, C. S. Su. 28/ 116, 163

Kumkum Kesara’s Description in Brihtrayi as Bahlika

Charaka Samhita: C. S. Chi. 23/ 102, C. S. Chi. 30/ 91

Sushruta Samhita: S. S. Ka. 6/ 3

Ashtanga Hridya: A. H. U. 34/ 46

Kumkum Kesara’s Description in Brihtrayi as Rudhira

Charaka Samhita: C. S. Su. 4/ 46

Kumkum Kesara’s Description in Brihtrayi as Sankocha

Charaka Samhita: C. S. Chi. 2- 3. 27

Historical Background of Kumkum Kesara

This is a herb with a tuberous root bearing a violet-colored flower. It is mainly cultivated in Kashmir. Sushruta and Vagbhata have described it under Eladi Gana. Bhavamisra quoted three varieties viz., Kasmira, Bahlika & Parasika. The Kasmira variety was considered the best. Acharya Thakurji has also reported Vriksa- Kunkuma (Euonymus tingens Wall) in which the basal part of the stem is covered by a layer of the saffron-colored part which is entirely a fungal tissue.

External Morphology of Kumkum Kesara

Habit: A herbaceous plant, perennial, with a height of 6 to 10 inches.

Leaves: Leaves of Kumkum Kesara are radical, tunnel-shaped, linear, and margin-curled, with wings of flowers covered with leaves. Scape covered with a spathe.

Inflorescence: Flowers of Kesara are violet, autumnal appearing with the leaves. The throat of the flowers of Kesara is perianth, bearded. Anthers yellow, Solitary, or together with 2 or 3 flowers, having fine essence and brown. Perianth of the flower of Kumkum Kesara i.e Crocus sativa are funnel-shaped, tubelike, and hairs are found in the throat region. Styles of stigma exerted outside, orange in color, apex divided into many. Style in flower is 1 cm. elongated. Stigmas generally red in color, 3 in number, and thread-like, stigmas of the flower of Kumkuma Kesara are known as saffron (Kumkuma or Kesara) which are practical thread-like (three in number) and visible in a flower.

Roots: The root of Kumkuma kesara is corm type, devoid of the stem; sheaths of corm closely reticulate, basal spathe embracing the scape- 2- valved.

Fruits: Fruit rectangular in shape; ovary, trilocular, three-chambered in which round shape seeds found, fruit a capsule.

Flowering and fruiting time

Post-rains and flowering during autumn and pre-cold season.

Distribution of Kumkuma Kesara

Kumkuma Kesara is native to southern Europe, and it is cultivated in Iran, Spain, France, Italy, Greece, China, and Turkey. In India, it is mainly and largely cultivated in Kashmir (Pampore and Kishtwar) in Jammu and Kashmir state.

Varieties of Kumkuma Kesara

Raja Nighantu has mentioned two varieties of Kumkuma Kesara:

  • Kumkuma
  • Trin Kumkuma

Bhavaprakasha Nighantu has mentioned three varieties of Kumkuma Kesara:

  • Kasmiraja – Best quality of Kumkuma Kesara
  • Bahlika- Medium quality of Kumkuma Kesara
  • Parsika- Inferior quality of Kumkuma Kesara

In the market sample, two types of Kumkuma Kesara are available:

  • Laccha
  • Mograa

Properties of Different Types of Kumkuma Kesara Mentioned by Bhava Parkasha Nighantu

Kasmiraja – Suksma Kesarayukta (Small stigma), Raktavarna (Red) Padmagandhi (Aroma like that of Lotus).

Bahlika – Sukla (White) or Pita varna (Yellow) Ketaki Gandha (Aroma like Pandanus) Suksma kesara (Small stigma).

Parasika – Madhugandha (Honey like odor), Isatpandura varna (Whitish in color) Sthulakesara (Bigger stigma).

Useful Part of Kumkuma Kesara

Dried stigma

Dried stigma of Mograa variety: The dried stigma of the Mograa variety is deep red with the style cut and removed beyond the length of 10 mm. The upper extremity of each stigma spreads out to form a flat lamina having a dentate margin. It has got a very strong characteristic odor and a slightly bitter taste.

Dried stigma of Laccha variety: The dried stigma of the Laccha variety is having a long, tubular gradually tapering style of yellowish color, up to 2.5 cm in length. It has got a strong characteristic odor and a bitter taste.

Important Phytoconstituent of Kumkuma Kesara

It contains a coloring glycoside crocin and another colorless picrocrocin. It yields volatile oil at 1% and fixed oil at 8- 13%. Crocin is a red-colored amorphous powder that is soluble in water and alcohol. It becomes blue when mixed in concentrated sulphuric acid, turns violet after time, and finally, it is red. It gives green color in nitric acid solution.

Adulteration in Kumkuma Kesara

Carthamus tinctorius Florets

Chemical Tests of Kumkuma Kesara

  • Add a drop of Sulphuric acid to the dry stigma, it turns blue, gradually changing to purple and finally purplish red.
  • Saffrons impart yellowish orange-brown color to water.

Collection of Kumkuma Kesara

The plants are raised from corms planted during July or August. The flowering takes about one year. Flowers are collected in the early morning in November and December, Stigma and Upper style portions are detached manually, and the drug is dried by artificial heat and stored in a dry place.

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Recent Research on Kumkum Kesara

  • The present study aimed to investigate the anti-hyperglycemic and protective potential of crocin, a pharmacologically active constituent of Crocus sativus L., in streptozotocin-induced diabetic rats. In conclusion, findings suggest that crocin has hypoglycemic and antioxidative properties in streptozotocin-induced diabetes and it may be useful in the management of diabetic patients. Rajaei Z, Hadjzadeh MA, Nemati H, Hosseini M, Ahmadi M, Shafiee S. Antihyperglycemic and antioxidant activity of crocin in streptozotocin-induced diabetic rats. J Med Food. 2013 Mar; 16 (3): 206- 10. doi 10. 1089/ jmf. 2012. 2407. E pub 2013 Feb 25.
  • In this study, they aimed to investigate the effects of crocin on MMP- 1, MMP- 3, and MMP- 13 expression in rabbit chondrocytes induced by interleukin- 1B (IL-1ß) and in an experimental rabbit model induced by anterior cruciate ligament transection. Findings suggest that the anti-inflammatory activity of crocin may be of potential value in the prevention and treatment of osteoarthritis. Ding O, Zhong H, Qi Y, Cheng Y, Li W, Yan S, Wang X. Anti-arthritic effects of crocin in interleukin 19- treated articular chondrocytes and cartilage in a rabbit osteoarthritic model. Inflammatory Res. 2013 Jan; 62 (1): 17. 25. doi 10. 1007/ 00011- 012-0546- 3. Epub 2012 Aug 18.
  • Patel, Sweta & Sarwat, Maryam & Khan, Tajdar. (2017). Mechanism Behind the Anti-Tumour Potential of Saffron (Crocus sativus L.): The Molecular Perspective. Critical Reviews in Oncology/Hematology. 115. 10.  1016/ j. criterion. 2017. 04. 010. Cancer is a disorder that has noted a significant rise in incidence worldwide and continues to be the largest cause of mortality. It has a dramatic impact on human life expectancy and quality of life despite the increase in technology and the treatments available for cancer patients. These new therapeutic options chemotherapy, radiotherapy, photolytic therapy, and catalytic therapy are known to have many adverse reactions and also no better positive outcomes than before. Hence, research is now focused more on utilizing the vast repertoire of traditional medicinal knowledge i.e., the use of flora for the treatment of cancer rather than the use of chemicals. One such herb is the Crocus sativus L., commonly known as Saffron, rich in carotenoids − crocin, crocetin, and safranin. Various studies have been carried out over the past few years to confirm the anti-cancer properties of saffron, both in vivo using animal models and in vitro using human malignant cell lines on various types of cancers with positive results. The proposed mechanism of action has also been worked upon. This review is aimed to provide a brief overview of the anti-tumor potential of saffron focusing on the molecular mechanism involved.
  • Lahmass, Iliass & Ouahhoud, Sabir & Elmansuri, Mohammed & Sabouni, Assia & Mohammed, Elyoubi & Benabbas, Redouane & Choukri, Mohammed & Saalaoui, Ennouamane. (2018). Determination of Antioxidant Properties of Six By-Products of Crocus sativus L. (Saffron) Plant Products. Waste and Biomass Valorization. 9. 10. 1007/ s12649- 017- 9851- y. Purpose Crocus sativus L. is one of the spices believed to possess antioxidant activities. The stigma of saffron has been widely used as a spice for culinary purposes, as a food colorant, and medicinal plant. In this research, we evaluate and compare the antioxidant properties of ethanolic extracts of six different by-products of the Crocus sativus plant including dry leaves, green leaves, corms, tunics, paths, and stigmas. Methods The antioxidant activity was evaluated using in vitro assays such as total antioxidant capacity, DPPH free radical, Scavenging of H2O2, FRAP, and β-carotene bleaching assay. Results- The results showed that all extracts possess antioxidant properties and scavenging activities. Extract from stigmas revealed lower activity than that of other by-products, corms extract showed the highest level of free radical-scavenging activity. Spathes extract showed the strangest protection from β-carotene bleaching among all extracts. Conclusions, therefore, all by-products produced from the harvesting of saffron stigma could be applied as a natural antioxidant source for biological activities. 
  • Ahmad Baba, Shoib & Malik, Aubid & Wani, Zahoor & Mohiuddin, Tabasum & Hamid, Zeeshan & Abbas, Nazia & Ashraf, Nasheeman. (2015). Phytochemical analysis and antioxidant activity of different tissue types of Crocus sativus and oxidative stress alleviating potential of saffron extract in plants, bacteria, and yeast. South African Journal of Botany. 99. 10. 1016/ j. sab. 2015. 03. 194. Crocus sativus L. belongs to the family Iridaceae and its stigma part which forms commercial saffron has been used as a spice and medicine ever since the Greek-Minoan civilization. Saffron is considered the most expensive spice in the world and the site for the biosynthesis of peculiar metabolites (apocarotenoids), responsible for its characteristic color, flavor, and aroma. There is enough literature citing the antioxidant properties of saffron metabolites, but most of the knowledge accumulated so far comes from the stigma part only, while other plant parts particularly the vegetative tissues have not been worked out. The present study was conducted to evaluate and compare the chemical composition and antioxidant activity of three different tissue types of Crocuses viz stigma, corm, and leaf. The phytochemical analysis carried out using LC-MS showed that the major constituents identified were flavonoids like kaempferol, taxifolin, naringenin, etc., and apocarotenoids including crocin, crocetin, and their derivatives. Also, the total phenolic, flavonoid, and carotenoid contents were determined. The antioxidant property of these tissue types was also investigated and compared by biochemical assays like DPPH, NBT, and FRAP. The ethanolic fraction of stigma demonstrated the strongest antioxidant activity which could be attributed to its highest content of phenolics and flavonoids. Stigma extract was further evaluated for its role in alleviating oxidative stress in plants, yeast, and bacteria. The results showed that stigma extracts reduced methyl viologen-induced chlorophyll damage, lipid peroxidation, and protein oxidation in plants thereby rendering them more tolerant to stress. It was also shown to alleviate H2O2-mediated oxidative stress tolerance in bacteria and yeast.
  • Arasteh, Ali & Aliyev, Ali & Khamnei, Saeed & Delazar, Abbas & Mesgari Abbasi, Mehran & Mehman navaz, Yousef. (2010). Effects of hydroethanolic extract of saffron (Crocus sativus) on serum glucose, insulin, and cholesterol levels in healthy male rats. Journal of Medicinal Plants. 4. 397- 402. Saffron and its constituents are reported to have a wide range of biological activities. To determine the hypoglycemic effect of hydro methanolic extract of saffron, which has rarely been dealt with in previous studies, and the hypolipidemic effect of saffron extract, we investigated the effects of a hydro-methanolic extract of saffron on healthy male rats. The present study also aimed at evaluating the effects of the saffron extract on the insulin secretory function of pancreatic β-cells. In this study, healthy male rats (n = 30) were divided into 3 groups of ten: The test group (saffron group), the sham group (physiologic serum group), and the normal group. The test group received 50 mg/ kg saffron extract through intra- peritoneal injection. The sham group was also intraperitoneally injected with 50 mg/ kg of physiologic serum solvent for 2 weeks. The daily injection was repeated at 10 am. Blood samples were obtained from the retro-orbital sinus before administration and on the 7th and 14th days of administration. The serum glucose and cholesterol levels were measured by the enzymatic method and insulin levels were measured using an insulin kit by ELISA method. The results showed that hydro methanolic extract of saffron on the 7th day of administration significantly decreased serum glucose in the saffron group without having any effects on serum cholesterol and insulin levels. On the 14th day of administration, we found a significant decrease in serum glucose and cholesterol levels in the saffron group. In addition, after 2 weeks, serum insulin in the test group significantly increased compared to the sham and normal groups. No changes were observed in serum glucose, cholesterol, and insulin levels in sham and normal groups on the 7th and 14th days of administration. These results suggest that saffron extract has hypoglycemic and hypolipidemic effects on healthy male rats. Moreover, the saffron extract could increase insulin secretion from pancreatic β- cells. Therefore, it should be considered in future therapeutic research.
  • In this study, the effects of saffron (Crocus sativus) stigma aqueous extract and two active constituents, crocin, and safranal, were investigated on blood pressure of normotensive and deoxycorticosterone acetate-induced hypertensive rats. Safranal is more important than crocin for lowering down blood pressure of rats. Imenshahidi M, Hosseinzadeh H, Javadpour Y. Hypotensive effect of aqueous saffron extract (Crocus sativus L.) and its constituents, safranal, and crocin, in normotensive and hypertensive rats Phytother Res. 2010 Jul; 24 (7): 990- 4. doi: 10. 11002/ ptr. 3044.
  • BUTNARIU, Monica & Quispe, Cristina & Herrera, Jesús & Sharifi-Rad, Javad & Singh, Laxman & Aborehab, Nora & Bouyahya, Abdelhakim & Venditti, Alessandro & Sen, Surjit & Acharya, Krishnendu & Bashiry, Moein & Ezzat, Shahira & Setzer, William & Martorell, Miquel & Mileski, Ksenija & Bagiu, Iulia & Anca Oana, Docea & Cho, Wi. (2022). The Pharmacological Activities of Crocus sativus L.: A Review Based on the Mechanisms and Therapeutic Opportunities of its Phytoconstituents. Oxidative Medicine and Cellular Longevity. 2022. 10. 1155/ 2022/ 8214821. Crocus species are mainly distributed in North Africa, Southern, and Central Europe, and Western Asia, used in gardens and parks as ornamental plants, while Crocus sativus L. (saffron) is the only species that is cultivated for edible purposes. The use of saffron is very ancient; besides its use as a spice, saffron has long been known also for its medical and coloring qualities. Due to its distinctive flavor and color, it is used as a spice, which imparts food preservative activity owing to its antimicrobial and antioxidant activity. This updated review discusses the biological properties of Crocus sativus L. and its phytoconstituents, their pharmacological activities, signaling pathways, and molecular targets, therefore highlighting it as a potential herbal medicine. Clinical studies regarding its pharmacologic potential in clinical therapeutics and toxicity studies were also reviewed. For this updated review, a search was performed in the PubMed, Science, and Google Scholar databases using keywords related to Crocus sativus L. and the biological properties of its phytoconstituents. From this search, only the relevant works were selected. The phytochemistry of the most important bioactive compounds in Crocus sativus L. such as crocin, crocetin, picrocrocin, and safranal, as also dozens of other compounds were studied and identified by various physicochemical methods. Isolated compounds and various extracts have proven their pharmacological efficacy at the molecular level and signaling pathways both in vitro and in vivo. In addition, toxicity studies and clinical trials were analyzed. The research results highlighted the various pharmacological potentials such as antimicrobial, antioxidant, cytotoxic, cardioprotective, neuroprotective, antidepressant, hypolipidemic, and antihyperglycemic properties and protection of retinal lesions. Due to its antioxidant and antimicrobial properties, saffron has proven effective as a natural food preservative. Starting from the traditional uses for the treatment of several diseases, the bioactive compounds of Crocus sativus L. have proven their effectiveness in modern pharmacological research. However, pharmacological studies are needed in the future to identify new mechanisms of action, pharmacokinetic studies, new pharmaceutical formulations for target transport, and possible interactions with allopathic drugs.
  • Milajerdi, Alireza & Djafarian, Kurosh & Hosseini, Benita. (2015). The toxicity of saffron (Crocus sativus L.) and its constituents against normal and cancer cells. Journal of Nutrition & Intermediary Metabolism. 3. 10. 1016/ j. jnim. 2015. 12. 332. Background and aims: Saffron is a spice with preventive and curative effects. This study aimed to review the toxicity of saffron extract and its constituents on normal and cancer cells. Methods: We searched the PubMed, Science direct, SID, and Magiran databases up to November 2015 using the following keywords: toxicity, saffron, crocin, crocetin, safranal, and cancer. Finally, 73 English and 5 Persian articles were selected to be recruited to be reviewed. Results: Saffron has selective toxicity against cancer cells, through inhibition of RNA and DNA synthesis and increasing apoptosis. Crocin has been considered the most important anticancer agent of saffron that plays a role in gene expression and apoptosis in cancer cells. Crocetin has an inhibitory effect on cancer cell growth that may be due to reduced synthesis of DNA, RNA, and protein in neoplastic cells, RNA polymerase II inhibition, and interaction with histone H1 and H1- DNA structures. Saffron and its crocin and crocetin have also shown anticancer and cancer-preventive effects in animal models of cancer. Safranal also has shown antitumor activity with low toxicity. On the other hand, the lethal dose of 50% (LD50) for the saffron and its constituents against normal cells can be very high. Conclusion: In conclusion, emerging evidence suggests that saffron extract and its crocin, crocetin, and safranal have a selective toxicity effect against cancer cells and also may have cancer preventive functions. However, Saffron and its constituent’s toxicity against normal cells is negligible and they are even non-toxic in oral administration.
  • This study aimed to investigate the antidepressant properties of stigmas and corms of Crocus sativus L. The aqueous ethanol extract of C. sativus corms was fractionated based on polarity. The results suggest that the low polarity parts of C. sativus corms should be considered as a new plant material for curing depression, which merits further studies regarding antidepressant-like activities of chemical compounds isolated from the two fractions and mechanism of action. Wang Y, Han T, Zhu Y, Zheng CJ, Ming OL, Rahman K, Qin LP. Antidepressant properties of bioactive fractions from the extract of Crocus sativus L. J Nat Med. 2010 Jan; 64 (1): 24- 30. doi 10. 1007/ s 11418- 009- 0360- 6. Epub 2009 Sep 29.
  • Sheng, Liang & Qian, Zhiyu & Zheng, Shuguo & Xi, Liang. (2006). Mechanism of hypolipidemic effect of crocin in rats: Crocin inhibits pancreatic lipase. European journal of pharmacology. 543. 116- 22. 10.1016/ j. tephra. 2006. 05. 038. The hypolipidemic mechanism of crocin, an active ingredient in Gardenia jasminoides Ellis and Crocus sativus L, was examined in rats. In diet-induced hyperlipidemic rats, a 10-day treatment with crocin significantly reduced serum triglyceride, total cholesterol, low-density lipoprotein (LDL) cholesterol, and very low-density lipoprotein (VLDL) cholesterol levels in the daily dose range of 25 to 100 mg/kg. Results of the modified fat-loading method indicated that crocin inhibited the absorption of fat and cholesterol and this inhibition is closely related to the hydrolysis of fat. In addition, the modified fat-balance method demonstrated that crocin increased the fecal excretion of fat and cholesterol in rats but had no influence on the elimination of bile acids. The results of the in-situ loop method and enzyme assay indicated that crocin could not directly block the absorption of cholesterol from rat jejunum but could selectively inhibit the activity of pancreatic lipase as a competitive inhibitor. These findings suggest that crocin yielded its hypolipidemic effect by inhibiting pancreatic lipase, leading to the malabsorption of fat and cholesterol.
  • S. In this study, the anxiolytic and hypnotic effects of saffron aqueous extract and its constituents crocin and safranal were studied in mice. The results showed that saffron aqueous extract and safranal have anxiolytic and hypnotic effects. Hosseinzadeh H, Noraei NB.  The anxiolytic and hypnotic effect of Crocus sativus aqueous extract and its constituents, crocin, and safranal, in mice. Phytother Res. 2009 Jun; 23 (6): 768- 74. doi 10. 1002/ ptr. 2597.
  • The effect of plant extract on macromolecular synthesis was examined in three human cell lines- A549 (derived from a lung tumor), W1-38 (normal lung fibroblasts), and VA- 13 (WI- 38 cells transformed in vivo by SV 40 tumor virus). Malignant cells were more sensitive than normal cells to the inhibitory effect of the extract on both DNA & RNA synthesis (BioFactors 1992, 4, 43).
  • Makhlouf, Hassane & Saksouk, Mariam & Habib, Jean & Chahine, Ramez. (2011). Determination of the antioxidant activity of saffron taken from the flower of Crocus sativus grown in Lebanon. AFRICAN JOURNAL OF BIOTECHNOLOGY. 10 (41). 8093- 8100. 10. 5897/ AJB11. 406. Since oxidative stress has been implicated in the most common cause of death, especially in the case of cancer and cardiovascular disease, natural substances and spices that show antioxidant effects merit a closer examination. Saffron is a yellow natural spice derived from the flower of Crocus sativus and used as a coloring agent in many foods worldwide. In this study, we determined the total polyphenols content in the Lebanese saffron and the antioxidant effects of different extracts from this saffron in vitro using electrolysis of physiological solution for generation of free radicals (FR) in the presence of colorimetric indicator N, N- di- ethyl- P- phenylenediamine; the absorbance was measured spectrophotometrically at 515 nm. Histopathological studies allowed us to observe the damages caused by FR in the isolated organs of hamsters (kidney, liver, lungs, and heart) and on the other hand the protection that saffron provided to these vital organs. By using assay kits, we evaluated the levels of lipid peroxidation and superoxide dismutase activity, the important free radical scavenging enzyme. The results showed that both boiled and soaked saffron at 0.45 mg/ml are highly effective against FR generated by electrolysis and against the damages caused to the organs tested as observed by light microscopy. Moreover, saffron significantly (p < 0.05) decreased lipid peroxidation and increased superoxide dismutase activity in all tissues used as compared to the control. We concluded that Lebanese saffron strongly protects vital organs against oxidative stress. 
  • Prajapati, Pk & Sharma, Rohit & Patigiri, Bj & Pk, & Prajapati, Pradeep. (2014). Clinical efficacy of Kumkumadi Ghrita prepared by Kesar and Nagakesar on Mukhadushika (Acne vulgaris). International Journal of Pharma Sciences and Research (IJPSR) 0975- 9492. 5. 806- 811. Introduction: Despite a large number of treatment options for Mukhdushika (Acne vulgaris), efforts are still carried out by medical society to bring out more effective treatment. Kumkumadi Ghrita (KG) is one of the highly valued formulations among Ayurvedic physicians, commonly recommended in Mukhdushika. Kesar (stigma of Crocus sativus Linn) is a prime ingredient in the formulation. Due to high cost and increased adulteration trends in
  • Kesar, another botanical ‘Nagakesar’ (stigma of Mesua ferrea Linn.) is suggested by Ayurvedic experts as a substitute, which has a relatively low cost and possesses similar therapeutic attributes to Kesar. However, no published work has been available to date on the comparative clinical efficacy of KG prepared by Kesar and Nagakesar. Aims and Objectives: To evaluate the comparative clinical efficacy of Kesaryukta (with Kesar) Kumkumadi Ghrita (KKG) and Nagakesar yukata (with Nagakesar) Kumkumadi Ghrita (NKG). Materials and Methods: Sixty known patients of Mukhdushika of both genders were selected. Both KKG and NKG were used as an external application by Abhyanga (massage) for 15 minutes and keep it for 10 minutes and then wash face with Besan (Gram powder) once a day, for 4 weeks duration. Suitable diet and lifestyle modifications were advised along with the therapy. The obtained data was analyzed statistically by applying paired ‘t-test. Results and conclusion: Both groups of KG were found effective in the treatment of Mukhdushika. Though, on signs and symptoms, KKG showed a comparatively slightly better effect; overall comparing the clinical efficacy of both groups, statistically, no major difference was found. Since NKG is highly cost-effective than KKG, the present study warrants the use of Nagakesar in place of Kesar for the preparation of KG.

Rasa Panchaka of Kumkum Kesara

Rasa (Taste)Katu (Pungent), Tikta (Bitter)
Guna (Virtue)Snigdha (Oily)
Virya (Potency)Ushana (Hot Potency) 
Vipaka (Post-Digestion)Katu (Pungent)

Dosha Karma of Kumkuma Kesara

Vata- Kapha Shamaka, Vata Hara due to Ushana Virya and Snigdha Guna. Kapha Hara because of Tikta, Katu Rasa, Ushana Virya and Katu Vipaka.

Karma (Actions) of Kumkuma Kesara

Varnya, Shotha Haram, Kotha Prashamana, Jantu Ghana, Madaka in high dosage, Vedana Sthapana, Chakshushya, Chardi Nigrehana, Dipaniya, Pachaniya, Rochana, grahi, Yakrit Uttejaka, Mastishaka Balya, Rakta Prasadaka, Hridya, Garbhashya Sankochaka, Vajikarna, Mutra Prasadna, Sheeta Prashmna, Sweda Janana, Varnya, Katu Pushtika, Mutra Janana, Rasayana, Dourgandhya Hara.

Karma (Actions) of Trina Kumkuma

Sopha Hara, Kustha Ghana, Ama Dosha Ghana, Kandughana

Ayurvedic Books on Allergies and Child Health

Prayogarha Vyadhi (Therapeutic indication) of Kumkum Kesara

Varna Vikriti, Kshudra Vikara, Vyanga, Nyaccha, Nilika, Pidika, Sirah Shula, Vrana Dristi Dourbalya, Mastiska Dourbalya Janita Vikara, Siraha Shula, Ardhava Bhedaka, Vata Vyadhi, Amavata, Nadisula, Agnimandya, Ajirna, Aruci, Atisara, Vamana, Yakrdvikara, Hriddourbalya, Rakta vikara,  Mutra krchra, Mutra Ghata, Dhavja Bhanga, Nnapunsakata, Kamasaitya, Garbhasaya Vikara, Prasavottar Vikara (Visodhana), Rajah Vikara, Rajorodha, Kstartava, Charma Vikara, Varna Vikara, Masurika, Jwara, Dourbalya.

Aamyik Paryog (Therapeutic Uses) of Kumkum Kesara

To pacify cold: Kunkuma, aguru, kasturi, nakha, ela, devadaru saileya, Chandana, tvak, musta, rasna, turuska, vaca and kustha-these applied separately or jointly as paste pacify cold. (Ashtanga Samgreha Chikitsa Sthana. 2. 87)

Shiro shool (Headache): Headache caused by pitta and rakta is alleviated by taking snuff of ghee cooked with Sarkara and Kumkuma. (Ashtanga Hridya Uttara Tantra. 24. 7, .62. 39, Gada Nigreha. 3. 1. 45, Sharangdhara Samhita. 3. 3. 32)

Vatavyadhi: Kumkuma, aguru, Patra, kustha, ela, tagara, etc. should be generally used in Vata Vyadhi. (Sushruta Samhita. Chikitsa Sthana. 4. 24- 26)

Mutra Ghata (Suppression of urine): Kumkuma 10 gm. should be put in honey water and kept overnight. In the morning it is taken which renders relief immediately. (Sushruta Samhita Uttara tantra. 58/ 31, Vrinda Madhava. 33/ 4)

Udavartta (caused by retention of urine): In such conditions, one should take the decoction of duralabha, infusion of kumkuma, or paste of karate seeds mixed with a little salt along with water. (Sushruta Samhita Uttara tantra. 55/ 25)

Facts About Kumkum Kesara

  • Before therapeutic use of the drug Kumkuma or saffron, the crude plant drug Kumkuma needs to be observed for its quality, grade, and genuineness before using it therapeutically and allowing the raw material for pharmaceutical process or any medicinal recipe since the costlier volubility of the drug is liable for admixture as well as a substandard crude drug carrying the possibility of any kind of malpractice against the standard pharmacopeial specification which may conform to specified characteristics of purity and authenticity. The stigmas of the flower of the plant (Crocus sativus (inn.), dried and thread-like stigmas, form the drug Kumkuma or Kesara. 
  • The raw material of the drug is tested for ascertaining its purity and quality. Stigmas are put into sulphuric acid, and they immediately turn blue, afterward, they change to purple and finally the stigmas become violet-red. The color intensity of genuine saffron is specifically tested. 
  • Material of the crude drug (saffron) 0.2 gm. (3/ 10 gram) is mixed in 100 ml. (c.c.) water and its solution becomes a water solution of potassium dichromate (0.1 percent) of yellow color. Some other tests in chemical screening are also suggested to confirm salient characteristics of genuine drug material of saffron. The color intensity of saffron crude drug is important in the test process to verify the nature of color. 
  • In case the sample of artificial (pseudo-colored) or impure crude drug 0.1gm. is well-mixed with water and slowly shaken for about 15 minutes. The mixture (solution) is filtered and then discoloring charcoal 1 gm. is added (well-mixed) and shaken. After ten minutes, it is filtered. Thus, the filtrate is found in a colorless substance. Another technique for testing unauthentic colors may be followed. 
  • A sample of saffron 10 mg. is mixed well in alcohol (95%) or methyl alcohol. This solution becomes greenish- yellow in color. A sample of genuine or pure saffron 10 mg. is mixed with ether or chloroform and the solution is observed almost colorless.
  • Similarly, the saffron crude sample becomes almost colorless when it is mixed in xylene, benzene, or carbon tetrachloride solvent. Two filter paper pieces are treated (dipped in) with fixed oil and glycerin and the saffron sample is kept between filter papers (pieces) and pressed. It will give translucent spots in case of impure saffron, and there will be no such spot if the saffron is pure and genuine (not artificially colored). Saffron as the raw drug is very prone to adulteration (admixture of substandard material, admixture of non-official parts and artificial crude material, etc.) of various kinds and nature on account of costlier drugs and valuable material produced in specific (restricted) zone of conventional farming for the indigenous source of supply (and also from import drug resources) of this precious drug item carrying possibilities of admixture and availability of the spurious quality of market drug saffron under trading of precious drugs commodities.
  • During the collection of saffron at the initial stage of procurement of its crude material, sometimes undesirable parts of the flowers such as styles, stamens, and strips of the corolla of the flower of source plant (Crocus sativus Linn. Kumkuma) saffron are admixture other than official part i.e., dried stigmas in accordance to pharmacopeial specification. The substandard material, exhausted and old parts of the crude drug are admixtures as faulty procurement and supply of low or inferior quality saffron which does not conform to an official drug standard. There is a practice to make adulteration of certain plant materials resembling saffron. Among the plants and their particular flower or another part (s), Kusumbha (Carthamus tinctorius Linn, Asteraceae) or Barren, Jaregul (Calendula officinalis Linn, Asteraceae) and some other similar plants material are adulterated in natural form or artificially colored state.
  • Sometimes faulty attempts are made to increase the weight of crude drugs by adding or treating saffron material with certain other liquids, powder solids etc. For instance, fixed oil, glycerin, sucrose, glucose, and other organic matters; and potassium or ammonium nitrate and other inorganic salts solution. In addition, some other unauthentic plant materials as well as faulty processes may be adopted as part of malpractices for adulteration in saffron.
  • The drug saffron or Kumkuma is a highly medicinal, reputed flavoring, and rich coloring agent among precious drugs, obtained from medicinal and aromatic plants of indigenous systems of medicine.
  • Kumkum or Kesara has therapeutic applications in several diseases, and it enters various medicinal recipes.

Benefits of Kumkum Kesara

  • It is employed as an ingredient in some formulations. Saffron is extensively used in perfumery and allied purposes including flavoring items for dietetic preparations (dishes).
  • As an effective drug, it is recommended in the treatment of fever, melancholia, impotency, catarrhal affections (especially in children), lumbar, neuralgic and rheumatic pains, asthma, dysmenorrhea, leucorrhea, piles, sexual weakness, depression, and other ailments. 
  • It is a good stimulant, aphrodisiac and nervine tonic. The drug has actions of aphrodisiac, diuretic, antiphlogistic, germicide, anodyne, stomachic, and aromatic. It is useful to check vomiting, headache, dermatosis, and other skin affections. 
  • Saffron is quite useful in diseases of the skin and especially cutaneous ailments caused by abnormal pigmentation or discoloration since it is effectively a promotor of luster and complexion of the body and skin. Saffron is, hence, esteemed for cosmetic purposes. 
  • In larger doses, it is hot, stimulant, aphrodisiac, and narcotic. Its smell is intense and odorous which may affect adversely if inhaled in excess.
  • The use of saffron within limited doses is generally of therapeutic utility. The addition of saffron with other drugs in any formulation activates its action on the heart and brain or makes it more effective regarding therapeutic potentialities including the action of saffron on different systems, organs, and functions of the body.

Matra (Therapeutic Administration and Dosage) of Kumkum Kesara

  • Churna (powder): 125- 500 mg

In some textbooks dosage between 62. 5 mg to 2 grams is mentioned.

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Classical Reference of Kumkum Kesara

Bhava Prakasha Nighantu Karpuraadi Varga- 74

Synonyms

कुंकुम घुसृनं रक्त काश्मीर॑ पीतकं वरम।

संकोच॑ पिशुनं धीर॑ बाह्लिकं शोणिताभिधम्‌ ।।

Bhava Prakasha Nighantu Karpuraadi Varga- 78

Properties and action

कुंकुम कटुक स्निग्ध॑ शिरोरूग व्रण जित। 

तिक्त॑ वमिहरं वर्ण्य व्यंग दोष त्रयापहम्‌ ।।

Dhanvantri Nighantu Chandanadi Varga- 12

Properties and actions

कुंकुम कटुक॑ तिक्तमुष्ण॑ श्लेष्म समीरजित्‌ ।

व्रण दृष्टि शिरोरोग विषह्वत्‌ कायकान्ति कृत्‌। 

Kaiydeva Nighantu Aushadi Varga, 1302

कुमकुम कटुक तिक्त॑ वर्ण्य व्रण विशोधनम्‌ ।

हन्ति दोषत्रय॑ हिक्का शिरोरोग वमिकृमीन्‌ ।।

Raja Nighantu Chandanadi Varga, 41

कुमकुम सुरभि तिक्त कटु उष्णं  कासवात कफकण्ठ रुजाघ्नम्‌ ।

मूर्ध शूलविष दोषनाशनं रोचनच्च तनु कान्तिकारकम्‌ ।।

Raja Nighantu Chandanadi Varga, 43

तृण कुमकुम – तृण कुंकुम कटूष्णं कफमारुत शोफनुत्‌ ।

कण्डूतिपामा कुष्ठामदोषघ्न॑ भास्कर परम। 

Priya Nighantu Shatpushpadi Varga, 39

सौगन्ध्यर्थमथापि शक्तिजनने संसेव्यते  कामिभिस्तिक्त॑ वर्ण्य मनुष्य मुक्तममलं त्वग्दोष दोषापहम्‌ ।।

Bhava Prakasha Nighantu Karpuraadi Varga- 75- 77

Varieties and their characteristics

काश्मीरदेशजे क्षेत्रे कुंकुम यादवेधी तत। 

सूक्ष्म केशर मारक्तं पद्म गंधी तद उत्तमम |

बाह्लीक देश संञ्जत कुंकुम पाण्डुर समृत्म |

केतकी गंध युक्तं तन्मध्यं सूक्ष्म केशरं ||

कुंकुम पारसीकं यन्मधुगन्धि तदीरितम।

ईषत्पाण्डुर वर्ण तद धम्म स्थूलकेशरम्‌ ।

Kaiydeva Nighantu Aushadi Varga, 1303- 1306

कौंकुंम॑ पुष्पमारक्त॑ गन्धवत्सूक्ष्म केशरम्‌ ।

काश्मीरेषु च संजातं पद्मगन्धि तदुत्तमम्‌ ।।

अतिस्थूल॑ लतारूप॑ मध्यमं कथयन्ति हि ।

अपाण्डुर॑ खरं चैव स्थूल केशरमेव च ।।

मध गन्धि च विज्ञेय॑ पारसीकं तु कुंकुम ।

बाह्लीक देश कुंकुम पाण्डुवर्णकम्‌ ।

केतकी गंध संयुक्तं सूक्ष्म केशर शोभितम्‌ ।।

Raja Nighantu Amradi Varga, 40- 41

ज्ञं कुंकुम अग्नि शेखरम असृज काश्मीरजम  पीतकं

काश्मीर रुधिरं वरज्ञ पिशुनं रक्त॑ शठं  शोणितम्‌।

वाह्लीक॑ घुसृणं वरेण्यमरुणं कालेयकं जागुड़ं

कान्त॑ वहिशिखञ्च केसरवरं गौर॑ कराचीरितम्‌ ||

Raja Nighantu Amradi Varga, 42- 43

कुंकुम गुणा:

कुड्डमं सुरभि तिक्तकटूष्ण॑ कास वातकफ कण्ठरुजा घनम |

मूर्ध शूल विष दोषनाशवं रोचनञ्च  तनुकान्ति कारकम्‌ ||

तृणकुड्डमम्‌ 

तृण कुमकुम तृणासर गन्धितृणं शोणितज् तृणपुष्पम्‌।

गन्धादिकम तृणोत तृण गौरम लोहितम च नव संज्ञकं ||

गुणा: 

तृण कुमकुम कटु उष्णं कफ मारुत शोफनुत |

कण्डु अतिपामा कुष्ठं दोषघ्नं भास्करं परम ||

Bhavaprakasha Mutra Ghata Adhikaram, 36- 36, Chakra Dutta, 33- 5

मूत्राघातें

जले कुमकुम कल्क॑ वा  क्षौद्रमुषित॑ निशि।

Bhava Parkasha, Kshudra Roga Adhikara, 61/ 46- 51

व्यंगाद्या 

क्षुद्र विकार शम्नाय (कुंकुमादय तैलं)

Chakra Dutta Kshudra Roga Chikitsa, 55- 63- 76

नीलिका पिडिका व्यंगादय: चिकित्सायां ( अभ्यंगयार्थ मुखाकन्तिदायक ) योगा:

प्रथम कुमकुमाद्य तैलम्‌

द्वितीय कुमकुमाद्य तैलम्‌

तृतीय कुंगूमाद्य तैलम्‌

Chakra Dutta Shiro Roga Chikitsa, 60- 40, Sharangdhara Samhita, 3- 8- 32

शिरोरोगाणां प्रतिकारार्थ कुमकुम लेप: 

सशर्कर कुंकुमजीमाज्य भृष्टं नस्यं विधेय॑ पवनासृगुत्थे ।

भ्रू शंख कर्णा शिरोअर्द्धशूले दिनाभि वृद्धिप्रभवे च रोगे ||

Ashtanga Hridya Uttara Tantra, 24/ 7

शर्करा कुमकुम शृतं घृतम पित्त सुगन्धये | 

Ashtanga Sngreha, Chikitsa Sthana, 2/ 87

शीतप्रशमने 

कुमकुम अगरु कस्तूरी निरवेल्ला सुरदारूभि |

शैलेय चाण्डा त्वड्मुस्तरास्त्रा पिवचामये: ||

पृथक प्रदेहा सर्वे वां शीतघना दूढकल्कित ||

Sushruta Samhita Chikitsa Sthana, 4/ 24, 26

वातव्याधौ 

कुमकुम अगरु पत्राणि कुष्ठ एला तगरापि च |

समासे नैव मादिनी योज्य अनिल रोगेषु ||

Sushruta Samhita Chikitsa Sthana, 55, 25

मूत्र रोधज उदावर्ते 

दुःस्पर्शा स्वरस वापी कषायं कुमकुम अस्य च |

एरवारु बीजं तोयं पिबेद वा अलवणी कृतं |

Sushruta Samhita Uttara Tantra, 58- 31, Vrinda Madhava 33/ 4

मूत्र घात

पिबेत कुमकुम कर्ष वा मधुदक समायुतम |

रात्रि पर्युषितम प्रातस्थत्ता सुखम वाप्नयूयात ||

Vishista Yoga (Name of Important Formulation)

  • Kumkumadi ghrita for Mukha Dushika and Siddhma
  • Kumkumadya Tailam for Vyanga and Nilika
  • Kesaradi Ghrita
  • Kesardi Vati
  • Pushyanuga Churna
  • Yakuti Rasa
  • Patranga Asava
  • Asana Eladi Taila
  • Naga Bhallabha Rasa
  • Karchooradi Churna

Contraindication and Side Effects of Kumkum Kesara

  • Study revealed that use of Kesara in dosage of 100 mg for 26 weeks is safe when taken as medicine.
  • Saffron or Kumkum kesara in high dosage is dangerous. If high dosage i.e more than 5 grams is consumed then it may cause poisoning, bleeding from nose, yellow appearance of eyes, skin and dosage in range of 12 grams to 20 grams can cause death.
  • In some cases, the use of Kesara in even less dosage may result in nausea, vomiting, drowsiness, stomach problems, etc.
  • Due to its Ushana Virya (hot potency), it should be used with caution.
  • Avoid the use of saffron during pregnancy especially during the first twelve weeks of pregnancy as it found that it may cause abortion due to uterine contraction and inducing bleeding. It can be used after 12 weeks of pregnancy but after consultation with your doctor.
  • No specific study on the use of Kesara in breastfeeding women has been done so if you want to use Kumkum Kesara during breastfeeding be sure to consult your doctor beforehand.

Suggestive Reading Regarding Crocus sativus

  • Khazdair MR, Boskabady MH, Hosseini M, Rezaee R, M Tsatsakis A. The effects of Crocus sativus (saffron) and its constituents on the nervous system: A review. Avicenna J Phytomed. 2015 Sep-Oct; 5 (5): 376- 91. PMID: 26468457; PMCID: PMC 4599112.
  • Sheng, Liang & Qian, Zhiyu & Zheng, Shuguo & Xi, Liang. (2006). Mechanism of hypolipidemic effect of crocin in rats: Crocin inhibits pancreatic lipase. European journal of pharmacology. 543. 116- 22. 10. 1016/ j. tephra. 2006. 05. 038.
  • El Midaoui A, Ghzaiel I, Vervandier-Fasseur D, Ksila M, Zarrouk A, Nury T, Khallouki F, El Hessni A, Ibrahimi SO, Latruffe N, Couture R, Kharoubi O, Brahmi F, Hammami S, Masmoudi-Kouki O, Hammami M, Ghrairi T, Vejux A, Lizard G. Saffron (Crocus sativus L.): A Source of Nutrients for Health and for the Treatment of Neuropsychiatric and Age-Related Diseases. Nutrients. 2022 Jan 29; 14 (3): 597. doi 10. 3390/ nu 14030597. PMID: 35276955; PMCID: PMC 8839854.
  • Siddiqui MJ, Saleh MSM, Basharuddin SNBB, Zamri SHB, Mohd Najib MHB, Che Ibrahim MZB, Binti Mohd Noor NA, Binti Mazha HN, Mohd Hassan N, Khatib A. Saffron (Crocus sativus L.): As an Antidepressant. J Pharm Bioallied Sci. 2018 Oct- Dec; 10 (4): 173- 180. doi: 10. 4103/ JPBS. JPBS_ 83_ 18. PMID: 30568374; PMCID: PMC 6266642.
  • Abdullaev, F. (2007). Biological Properties and Medicinal Use of Saffron (Crocus sativus L.). Acta Horticulturae. 739. 10. 17660/ ActaHortic. 2007. 739. 44.
  • Mzabri, Btissam & Addi, Mohamed & Berrichi, Abdelbasset. (2019). Traditional and Modern Uses of Saffron (Crocus Sativus). Cosmetics. 6. 63. 10. 3390/ cosmetics 6040063.
  • Gambella, Filippo. (2013). “Perspectives in the mechanization of saffron (Crocus Sativus L.)”. International Journal of Mechanics and Control, ISSN: 1590- 8844, Vol. 14. 3 – 8.
  • Saeidnia, Soodabeh. (2012). Future Position of Crocus sativus as a Valuable Medicinal Herb in Phytotherapy. Pharmacognosy Journal. 27. 71. 10. 5530/ pj. 2012. 27. 12.
  • Hamidpour, Rafie & Hamidpour, Soheila & Hamidpour, Mohsen & Shahlari, Mina. (2013). Effect of Crocus sativus and its active compounds for the treatment of several diseases: A review. International Journal of Case Reports and Images. 4. 666. 10. 5348/ ijcri- 2013- 12- 407- RA- 1.
  • Vedpathak, Surendra & Vaibhav, Bapat & Sharma, Siddharth & Patel, Kunal. (2022). Fixing the Number of Ingredients of Kumkuma Nasya (Saffron Nasal Medication). 9. 1- 6.
  • Ahmad Baba, Shoib & Malik, Aubid & Wani, Zahoor & Mohiuddin, Tabasum & Hamid, Zeeshan & Abbas, Nazia & Ashraf, Nasheeman. (2015). Phytochemical analysis and antioxidant activity of different tissue types of Crocus sativus and oxidative stress alleviating potential of saffron extract in plants, bacteria, and yeast. South African Journal of Botany. 99. 10.1016/ j. saj. 2015. 03.194.
  • Abadibavil, Dina & Dashti, Sareh. (2021). Investigating the Effect of Saffron on Anxiety, Fatigue, Labor Pain and Vaginal Childbirth: Review Article. Malaysian Journal of Medicine and Health Sciences. 2636- 9346.
  • Tiwari, Vinita & Morya, Gyan Chand. (2018). A REVIEW STUDY ON THE THERAPEUTIC POTENTIAL OF SOME FLOWERS OF AYURVEDA. International Journal of Research in Ayurveda and Pharmacy. 9. 98- 102. 10. 7897/ 2277- 4343. 094120.
  • Kumar, Sanjay & Jawaid, Talha & Dubey, Sarvesh. (2011). Therapeutic Plants of Ayurveda; A Review on Anticancer. Pharmacognosy Journal. 3. 1–11. 10. 5530/jp. 2011. 23. 1.
  • Prajapati, Pk & Sharma, Rohit & Patigiri, Bj & Pk, & Prajapati, Pradeep. (2014). Clinical efficacy of Kumkumadi Ghrita prepared by Kesar and Nagakesar on Mukhadushika (Acne vulgaris). International Journal of Pharma Sciences and Research (IJPSR) 0975- 9492. 5. 806- 811.
  • Mall, Tej. (2017). SAFFRON-A TREASURE OF THE ANCIENT MEDICINE CHEST-AN OVERVIEW. World Journal of Pharmaceutical Research. 1604- 1623. 10. 20959/ wjpr 20174- 8285.
  • Singh Sankhla, Mahipal. (2020). Forensic Identification of Fake & Genuine Saffron (Kesar) from Local Market of Greater Noida. Forensic Science & Addiction Research. 5. 10. 31031/ FSAR. 2019. 05. 000615.
  • Singletary, Keith. (2020). Saffron: Potential Health Benefits. Nutrition Today. 55. 294- 303. 10.1097/ NT. 0000000000000449.
  • Kumar, Amit & Devi, Mamta & Kumar, Rakesh & Kumar, Sanjay. (2022). Introduction of high-value Crocus sativus (saffron) cultivation in non-traditional regions of India through ecological modeling. Scientific Reports. 12. 10. 1038/ s41598- 022- 15907- y.
  • Bathaie, S. Zahra & Mousavi, S. Zeinab. (2010). New Applications and Mechanisms of Action of Saffron and its Important Ingredients. Critical reviews in food science and nutrition. 50. 761- 86. 10. 1080/ 10408390902773003.
  • Zeka, Keti & Arroo, Randolph. (2016). Saffron crocus (Crocus sativus L.) as a source of kaempferol.
  • Arasteh, Ali & Aliyev, Ali & Khamnei, Saeed & Delazar, Abbas & Mesgari Abbasi, Mehran & Mehmannavaz, Yousef. (2010). Effects of hydroethanolic extract of saffron (Crocus sativus) on serum glucose, insulin, and cholesterol levels in healthy male rats. Journal of Medicinal Plants. 4. 397- 402.
  • Makhlouf, Hassane & Saksouk, Mariam & Habib, Jean & Chahine, Ramez. (2011). Determination of the antioxidant activity of saffron taken from the flower of Crocus sativus grown in Lebanon. AFRICAN JOURNAL OF BIOTECHNOLOGY. 10(41). 8093- 8100. 10. 5897/ AJB11. 406.
  • Zeka, Keti & Ruparelia, Ketan & Continenza, Maria & Androutsopoulos, Vasilis & Veglio, Francesco & Arroo, Randolph. (2015). Petals of Crocus sativus L. as a potential source of the antioxidants crocin and kaempferol. Fitoterapia. 107. 128-134. 10. 1016/ j. fitote. 2015. 05. 014.
  • BUTNARIU, Monica & Quispe, Cristina & Herrera, Jesús & Sharifi-Rad, Javad & Singh, Laxman & Aborehab, Nora & Bouyahya, Abdelhakim & Venditti, Alessandro & Sen, Surjit & Acharya, Krishnendu & Bashiry, Moein & Ezzat, Shahira & Setzer, William & Martorell, Miquel & Mileski, Ksenija & Bagiu, Iulia & Anca Oana, Docea & Cho, Wi. (2022). The Pharmacological Activities of Crocus sativus L.: A Review Based on the Mechanisms and Therapeutic Opportunities of its Phytoconstituents. Oxidative Medicine and Cellular Longevity. 2022. 10. 1155/ 2022/ 8214821.
  • Wani, Bilal & Hamza, Amina & Mohiddin, Fayaz. (2011). Saffron: A repository of medicinal properties. Journal of Medicinal Plants Research. 5. 2131- 2135.
  • Khazdair, Mohammad & Boskabady, Mohammad Hossein & Hosseini, M.M. & Rezaee, Ramin & Tsatsakis, Aristidis. (2015). The effects of Crocus sativus (saffron) and its constituents on nervous system: A review. Avicenna journal of phytomedicine. 5. 376- 91.
  • Serghini, Mohammed & Khalid, Lagram & Ben El Caid, Mohamed & Lachheb, Mohamed & Atyane, L.H. & Salaka, L. & Youssef, Karra. (2017). Saffron ( Crocus sativus ): current state of scientific research. Acta Horticulturae. 79- 86. 10. 17660/ Acta Hortic. 2017. 1184. 12.
  • Farhan, Syed & Shamsi, Shariq & Alam, Md Tanwir & Perveen, Aisha. (2020). Saffron (Crocus sativus L.): A Review of its Ethnopharmacological value. American Journal of PharmTech Research. 10. 41-58. 10. 46624/a ptr. 2020. v10. i4. 005.
  • Srivastava, R. & Ahmad, Hafsa & Dixit, Rohit Kumar & Panjwani, Dharamveer & Saraf, Shubhini. (2010). Crocus sativus L.: A comprehensive review. Pharmacognosy Reviews. 4. 200- 208. 10. 4103/ 0973- 7847. 70919.
  • Setayesh L, Ashtary-Larky D, Clark CCT, Rezaei Kelishadi M, Khalili P, Bagheri R, Asbaghi O, Suzuki K. The Effect of Saffron Supplementation on Blood Pressure in Adults: A Systematic Review and Dose-Response Meta-Analysis of Randomized Controlled Trials. Nutrients. 2021 Aug 9; 13 (8): 2736. doi 10. 3390/ nu 13082736. PMID: 34444896; PMCID: PMC8398601.
  • Prajapati PK, Sharma R, Amrutia A, Patgiri BJ. Physicochemical Screening and Shelf- Life Evaluation of Kumkumadi Ghrita Prepared using Kesara and Nagakesara. Anc Sci Life. 2017 Jan- Mar; 36 (3): 129- 135. doi: 10. 4103/ asl. ASL_ 49_ 15. PMID: 28867856; PMCID: PMC 5566823.
  • Srivastava R, Ahmed H, Dixit RK, Dharamveer, Saraf SA. Crocus sativus L.: A comprehensive review. Pharmacognosy Rev. 2010 Jul; 4 (8): 200- 8. doi 10. 4103/ 0973- 7847. 70919. PMID: 22228962; PMCID: PMC 3249922.
  • Lu C, Ke L, Li J, Zhao H, Lu T, Mentis AFA, Wang Y, Wang Z, Polissiou MG, Tang L, Tang H, Yang K. Saffron (Crocus sativus L.) and health outcomes: a meta-research review of meta-analyses and evidence mapping study. Phytomedicine. 2021 Oct; 91: 153699. doi 10. 1016/ j. rhymed. 2021. 153699. Epub 2021 Aug 8. PMID: 34419735.
  • Kermani T, Kazemi T, Molki S, Ilkhani K, Sharifzadeh G, Rajabi O. The Efficacy of Crocin of Saffron (Crocus sativus L.) on the Components of Metabolic Syndrome: A Randomized Controlled Clinical Trial. J Res Pharm Pract. 2017 Oct-Dec; 6 (4): 228- 232. doi 10. 4103/jump. JRPP_ 17_ 26. PMID: 29417083; PMCID: PMC 5787909.
  • Khorasany AR, Hosseinzadeh H. Therapeutic effects of saffron (Crocus sativus L.) in digestive disorders: a review. Iran J Basic Med Sci. 2016 May; 19 (5): 455-69. PMID: 27403251; PMCID: PMC 4923465.
  • Omidkhoda SF, Hosseinzadeh H. Saffron and its active ingredients against human disorders: A literature review on existing clinical evidence. Iran J Basic Med Sci. 2022 Aug; 25 (8): 913- 933. doi 10. 22038/ IJBMS. 2022. 63378. 13985. PMID: 36159329; PMCID: PMC 9464341.
  • Maqbool Z, Arshad MS, Ali A, Aziz A, Khalid W, Afzal MF, Bangar SP, Addi M, Hano C, Lorenzo JM. Potential Role of Phytochemical Extract from Saffron in Development of Functional Foods and Protection of Brain-Related Disorders. Oxid Med Cell Longev. 2022 Sep 22; 2022: 6480590. doi 10. 1155/ 2022/ 6480590. PMID: 36193081; PMCID: PMC 9526642.
  • Mollazadeh H, Emami SA, Hosseinzadeh H. Razi’s Al-Hawi and saffron (Crocus sativus): a review. Iran J Basic Med Sci. 2015 Dec; 18 (12): 1153- 66. PMID: 26877844; PMCID: PMC 4744354.
  • José Bagur M, Alonso Salinas GL, Jiménez-Monreal AM, Chaouqi S, Llorens S, Martínez-Tome M, Alonso GL. Saffron: An Old Medicinal Plant and a Potential Novel Functional Food. Molecules. 2017 Dec 23; 23 (1): 30. doi 10. 3390/ molecules 23010030. PMID: 29295497; PMCID: PMC 5943931.
  • Patel, Sweta & Sarwat, Maryam & Khan, Tjader. (2017). Mechanism Behind the Anti-Tumor Potential of Saffron (Crocus sativus L.): The Molecular Perspective. Critical Reviews in Oncology/Hematology. 115. 10. 1016/ j. criterion. 2017. 04. 010.
  • Milajerdi, Alireza & Djafarian, Kurosh & Hosseini, Benita. (2015). The toxicity of saffron (Crocus sativus L.) and its constituents against normal and cancer cells. Journal of Nutrition & Intermediary Metabolism. 3. 10. 1016/ j. jnim. 2015. 12. 332.

References

  • Agnivesha, Charaka, Dridhabala. In: Charaka Samhita, ed. Vaidya Jadavaji Trikamji Aacharya., editor. Varanasi: Chaukhamba Sanskrit Sansthan; 2009. 
  • Sushruta. In: Sushruta Samhita, Sutra Sthana, ed. Vaidya Jadavji Trikamji Acharya., editor. Varanasi: Choukhambha Orientalia; 2005. 
  • Vagbhata. In: Ashtanga Hrudaya, 9th ed. Anna Moreshwar Kunte, Krishnashastri Navarre, Harishastri, editors. Varanasi: Choukhambha Orientalia; 2005.
  • Bhavamishra. In: Bhava Prakasha Nighantu, Karpuraadi Varga 11th ed. part 2. Brahma Shankara Mishra., editor. Varanasi: Choukhambha Bharati Academy; 2009. 
  • Bhavprakasha, commentary by Bulusu Sitaram, forwarded by K.C.Chunekar
  • Sharma PV, Kaideva Nighantu. Aushadhi Varga. Chaukhamba Orientalia, Varanasi; 2006:
  • Tripathi I., Raja Nighantu, Chandandi Varga, Chaukhamba Krishnadas Academy; Varanasi; 2010
  • Dhanwantri Nighantu, Chandandi Varga, Chaukhamba Krishnadas Academy; Varanasi.
  • Priya Nighantu by P. V. Sharma, Shatpushpadi Varga Chaukhamba Krishnadas Academy; Varanasi.
  • Dr. Gyanendra Pandey, Dravyaguna Vigyana, reprint 2012, Chawkhamba Krishnadas Academy
  • K. Niteshwar Dravyaguna Vigyan, reprint 2017.
  • Dr. J.L.N. Sastry and Dr. B.S. Sastry, Dravyaguna Vigyana, Chaukhambha Orientalia, Varanasi.
  • Chakrapanidatta, Chakradatta with the vaidaya Prabha hindi commentary by indra deva tripathi, chaukambha sanskrita sansthan, varanasi 2nd Edition, 1994.

Ayurveda is an Indian system of medicine that is popular since ancient times. Dr. Gupta’s IAFA® has been conducting research studies to find out different phytoconstituents of herbs and their action in the body. Such knowledge acquired by our experts is used in the preparation of medicines and providing the treatment facilities safely and effectively. IAFA® is the provider of safe and effective treatment for a wide range of diseases, mainly allergic diseases all based on Ayurveda.

Dr. Sahil Gupta completed his Bachelor of Ayurveda in Medicine and Surgery (B.A.M.S.) and Master’s Degree in Health Administration (MHA) India. He is Registered Ayurvedic Doctor & Vaidya in India having Registration No. 23780. He is the CEO and founder of IAFA. After completing BAMS, Dr. Sahil Gupta started practicing Ayruveda by giving prime importance to allergic disorders management. He became the first Ayurvedic doctor to cure Food Allergies through Ayurveda. Read More About Dr. Sahil Gupta.

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