Talk:Shalmali: Difference between revisions
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'''[https://en.wikipedia.org/wiki/Bombax_ceiba Bombax ceiba L.]''' (syn. | '''[https://en.wikipedia.org/wiki/Bombax_ceiba Bombax ceiba L.]''' (syn. ''Bombax malabarica'' D.C.), popularly known as '''Shalmali''' (Silk cotton tree), is a large, deciduous tree native to tropical regions of Asia, Australia, and Africa. It is widely revered in [[Ayurveda]] as a prominent cooling, astringent, and healing agent, traditionally utilized for managing internal hemorrhages, inflammatory skin conditions, burning sensations, and wound healing. | ||
== English name == | == English name == | ||
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== Phytochemical Composition == | == Phytochemical Composition == | ||
The | The best-characterised constituent of ''Bombax ceiba'' (syn. ''Bombax malabaricum'') leaves is '''mangiferin''', a xanthone C-glucoside. Mangiferin was isolated from the leaves by repeated column chromatography of the n-butanol fraction of the 70% ethanol extract and identified by UV, NMR and mass spectrometry. It proved identical to the compound earlier reported as the flavonol C-glycoside "shamimin", whose structure was therefore revised.<ref name="Shahat2003">{{cite journal |last1=Shahat |first1=A. A. |last2=Hassan |first2=R. A. |last3=Nazif |first3=N. M. |last4=Van Miert |first4=S. |last5=Pieters |first5=L. |last6=Hammuda |first6=F. M. |last7=Vlietinck |first7=A. J. |year=2003 |title=Isolation of mangiferin from Bombax malabaricum and structure revision of shamimin |journal=Planta Medica |volume=69 |issue=11 |pages=1068–1070 |doi=10.1055/s-2003-45161}}</ref> | ||
== Pharmacological Activities & Therapeutic Efficacy == | == Pharmacological Activities & Therapeutic Efficacy == | ||
=== | === Anti-diabetic and Hypolipidaemic Activity (Prameha) === | ||
* ''' | * '''Scientific Evidence:''' A bark extract of ''Bombax ceiba'' was given orally to normal and streptozotocin-induced diabetic rats at 200, 400 and 600 mg/kg/day for 21 days. The 600 mg/kg dose produced the most significant (p<0.001) hypoglycaemic and hypolipidaemic effects, including lower total cholesterol and triglycerides in severely diabetic rats. GC-MS studies confirmed triterpenoid compounds in the extract, which the authors suggest may account for the activity.<ref name="Bhavsar2013">{{cite journal |last1=Bhavsar |first1=C. J. |last2=Talele |first2=G. S. |year=2013 |title=Potential anti-diabetic activity of Bombax ceiba |journal=Bangladesh Journal of Pharmacology |volume=8 |issue=2 |pages=102–106 |doi=10.3329/bjp.v8i2.13701}}</ref> | ||
=== Anti- | === Anti-arthritic and Anti-inflammatory Activity === | ||
* ''' | * '''Scientific Evidence:''' In Wistar rats with Freund's complete adjuvant-induced arthritis, a 70% ethanolic extract of the aerial parts of ''Bombax ceiba'' (200 and 400 mg/kg) significantly inhibited paw oedema, reduced the pro-inflammatory cytokines TNF-α and IL-6, and reduced histopathological changes in the joint over 28 days. The authors concluded that the findings support the traditional use of the plant in arthritis.<ref name="Posinasetty2023">{{cite journal |last1=Posinasetty |first1=B. |last2=Chikatipalli |first2=R. |last3=Chenchula |first3=S. |last4=Kuttiappan |first4=A. |last5=Swapna |first5=G. |last6=Lakshmi |first6=G. N. A. |last7=Audinarayana |first7=N. |year=2023 |title=Anti-arthritic efficacy of Bombax ceiba ethanolic extract in a murine model for rheumatoid arthritis using in vivo, in vitro and radiological analysis |journal=Bioinformation |volume=19 |issue=8 |pages=833–839 |doi=10.6026/97320630019833 |pmid=37908617}}</ref> | ||
* '''Scientific Evidence:''' | |||
=== Antioxidant, Hepatoprotective and Analgesic Activity === | |||
* '''Scientific Evidence:''' Mangiferin obtained from methanolic extracts of ''Bombax ceiba'' leaves showed strong antioxidant activity in the DPPH assay (EC50 5.8 ± 0.96 µg/mL), comparable to rutin, and protected against carbon tetrachloride-induced liver injury in vivo. It also produced a significant analgesic effect in acetic acid-induced writhing and hot-plate tests in mice. The plant extracts and mangiferin did not show acute anti-inflammatory activity in that study.<ref name="Dar2005">{{cite journal |last1=Dar |first1=A. |last2=Faizi |first2=S. |last3=Naqvi |first3=S. |last4=Roome |first4=T. |last5=Zikr-ur-Rehman |first5=S. |last6=Ali |first6=M. |last7=Firdous |first7=S. |last8=Moin |first8=S. T. |year=2005 |title=Analgesic and antioxidant activity of mangiferin and its derivatives: the structure activity relationship |journal=Biological and Pharmaceutical Bulletin |volume=28 |issue=4 |pages=596–600 |doi=10.1248/bpb.28.596}}</ref> | |||
=== Hypotensive Activity === | |||
* '''Scientific Evidence:''' The C-flavonol glucoside shamimin (later shown to be mangiferin) from ''Bombax ceiba'' leaves was a significant hypotensive agent in Sprague-Dawley rats at 15, 3 and 1 mg/kg, and showed significant hypoglycaemic activity at 500 mg/kg.<ref name="Saleem1999">{{cite journal |last1=Saleem |first1=R. |last2=Ahmad |first2=M. |last3=Hussain |first3=S. A. |last4=Qazi |first4=A. M. |last5=Ahmad |first5=S. I. |last6=Qazi |first6=M. H. |last7=Ali |first7=M. |last8=Faizi |first8=S. |last9=Akhtar |first9=S. |last10=Husnain |first10=S. N. |year=1999 |title=Hypotensive, hypoglycaemic and toxicological studies on the flavonol C-glycoside shamimin from Bombax ceiba |journal=Planta Medica |volume=65 |issue=4 |pages=331–334 |doi=10.1055/s-1999-14060 |pmid=10364838}}</ref> | |||
== Safety, Toxicity, and Dosage == | == Safety, Toxicity, and Dosage == | ||
* '''Acute Toxicity:''' | * '''Acute Toxicity:''' In the study of shamimin, no mortality occurred in mice at 1 g/kg, whereas 500 mg/kg was a lethal dose in rats; the safety of crude extracts in humans has not been established in the studies cited here.<ref name="Saleem1999"/> | ||
== Summary of Therapeutic Profile == | == Summary of Therapeutic Profile == | ||
{| class="wikitable sortable" style="text-align: left;" | {| class="wikitable sortable" style="text-align: left;" | ||
|+ Therapeutic Applications of | |+ Therapeutic Applications of ''Bombax ceiba'' | ||
! Indication | ! Indication | ||
! Active Biomolecules | ! Active Biomolecules | ||
! Primary Pharmacological Action | ! Primary Pharmacological Action | ||
|- | |- | ||
| ''' | | '''Diabetes (Prameha)''' | ||
| | | Triterpenoids (bark extract) | ||
| | | Hypoglycaemic, hypolipidaemic (rat model) | ||
|- | |||
| '''Arthritis''' | |||
| Ethanolic extract of aerial parts | |||
| Reduced paw oedema, TNF-α and IL-6 (rat model) | |||
|- | |- | ||
| ''' | | '''Oxidative stress, liver injury, pain''' | ||
| | | Mangiferin | ||
| | | Antioxidant, hepatoprotective, analgesic (animal models) | ||
|- | |- | ||
| ''' | | '''Hypertension''' | ||
| | | Shamimin (mangiferin) | ||
| | | Hypotensive (rat model) | ||
|} | |} | ||
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<ref name="CharakSamhitaVol2">Acharya Vidyadhar Shukla, Prof. Ravidatta Tripathi, Charaka Samhita Vol. 2, Reprint 2006, Chaukhambha Sanskrit Pratishthan, Chikitsa Sthana, chapter no. 14, verse no. 188-192, p. 343.</ref> | <ref name="CharakSamhitaVol2">Acharya Vidyadhar Shukla, Prof. Ravidatta Tripathi, Charaka Samhita Vol. 2, Reprint 2006, Chaukhambha Sanskrit Pratishthan, Chikitsa Sthana, chapter no. 14, verse no. 188-192, p. 343.</ref> | ||
<ref name="Sunishannaka">Acharya Vidyadhar Shukla, Prof. Ravidatta Tripathi, Charaka Samhita Vol. 2, Reprint 2006, Chaukhambha Sanskrit Pratishthan, Chikitsa Sthana, chapter no. 14, verse no. 235-242, p. 349.</ref> | <ref name="Sunishannaka">Acharya Vidyadhar Shukla, Prof. Ravidatta Tripathi, Charaka Samhita Vol. 2, Reprint 2006, Chaukhambha Sanskrit Pratishthan, Chikitsa Sthana, chapter no. 14, verse no. 235-242, p. 349.</ref> | ||
<ref name=" | <ref name="Shahat2003">{{cite journal |last1=Shahat |first1=A. A. |last2=Hassan |first2=R. A. |last3=Nazif |first3=N. M. |last4=Van Miert |first4=S. |last5=Pieters |first5=L. |last6=Hammuda |first6=F. M. |last7=Vlietinck |first7=A. J. |year=2003 |title=Isolation of mangiferin from Bombax malabaricum and structure revision of shamimin |journal=Planta Medica |volume=69 |issue=11 |pages=1068–1070 |doi=10.1055/s-2003-45161}}</ref> | ||
<ref name=" | <ref name="Bhavsar2013">{{cite journal |last1=Bhavsar |first1=C. J. |last2=Talele |first2=G. S. |year=2013 |title=Potential anti-diabetic activity of Bombax ceiba |journal=Bangladesh Journal of Pharmacology |volume=8 |issue=2 |pages=102–106 |doi=10.3329/bjp.v8i2.13701}}</ref> | ||
<ref name="Posinasetty2023">{{cite journal |last1=Posinasetty |first1=B. |last2=Chikatipalli |first2=R. |last3=Chenchula |first3=S. |last4=Kuttiappan |first4=A. |last5=Swapna |first5=G. |last6=Lakshmi |first6=G. N. A. |last7=Audinarayana |first7=N. |year=2023 |title=Anti-arthritic efficacy of Bombax ceiba ethanolic extract in a murine model for rheumatoid arthritis using in vivo, in vitro and radiological analysis |journal=Bioinformation |volume=19 |issue=8 |pages=833–839 |doi=10.6026/97320630019833 |pmid=37908617}}</ref> | |||
<ref name="Dar2005">{{cite journal |last1=Dar |first1=A. |last2=Faizi |first2=S. |last3=Naqvi |first3=S. |last4=Roome |first4=T. |last5=Zikr-ur-Rehman |first5=S. |last6=Ali |first6=M. |last7=Firdous |first7=S. |last8=Moin |first8=S. T. |year=2005 |title=Analgesic and antioxidant activity of mangiferin and its derivatives: the structure activity relationship |journal=Biological and Pharmaceutical Bulletin |volume=28 |issue=4 |pages=596–600 |doi=10.1248/bpb.28.596}}</ref> | |||
<ref name="Saleem1999">{{cite journal |last1=Saleem |first1=R. |last2=Ahmad |first2=M. |last3=Hussain |first3=S. A. |last4=Qazi |first4=A. M. |last5=Ahmad |first5=S. I. |last6=Qazi |first6=M. H. |last7=Ali |first7=M. |last8=Faizi |first8=S. |last9=Akhtar |first9=S. |last10=Husnain |first10=S. N. |year=1999 |title=Hypotensive, hypoglycaemic and toxicological studies on the flavonol C-glycoside shamimin from Bombax ceiba |journal=Planta Medica |volume=65 |issue=4 |pages=331–334 |doi=10.1055/s-1999-14060 |pmid=10364838}}</ref> | |||
}} | }} | ||
[[Category: Database of herbs and minerals | Herbs]] | [[Category: Database of herbs and minerals | Herbs]] | ||