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MeSH Review

Embelia

 
 
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High impact information on Embelia

  • (Asteraceae) seeds and Embelia ribes Burm (Myrsinaceae) fruits; group D with 183 mg/kg BW of an aqueous ethanol extract of the whole plants of Fumaria parviflora Lam [1].
  • The effects of embelin (50 mg/kg/day), a benzoquinone derivative of Embelia ribes, and the effects of curcumin (100 mg/kg/day), the active principle of Curcuma longa, against N-nitrosodiethylamine (DENA)-initiated and phenobarbital (PB)-promoted hepatocarcinogenesis were studied in Wistar rats [2].
  • An ayurvedic contraceptive--pippaliyadi vati, containing equal parts of powdered seeds or fruit berries of Embelia ribes, fruit of Piper longum and borax powder was fed orally to two groups of pregnant rats: 2.5 times to one and five times to the other; the recommended dose for humans [3].
  • Intraperitoneal administration of the methanol extract of Embelia schiperi (ES) to normal mice caused a significant decrease in blood glucose (p < 0.01) and a significant increase in triglycerides 4 hours after administration at 100 mg/kg (p < 0.01) [4].
  • The toluene fraction of Embelia keniensis methanol extract (TS) showed hypoglycemic and lipid lowering activity 7 hours after intraperitoneal administration at 100 mg/kg [4].
 

Associations of Embelia with chemical compounds

References

  1. The anthelmintic efficacy of five plant products against gastrointestinal trichostrongylids in artificially infected lambs. Hördegen, P., Hertzberg, H., Heilmann, J., Langhans, W., Maurer, V. Vet. Parasitol. (2003) [Pubmed]
  2. Chemopreventive effects of embelin and curcumin against N-nitrosodiethylamine/phenobarbital-induced hepatocarcinogenesis in Wistar rats. Sreepriya, M., Bali, G. Fitoterapia (2005) [Pubmed]
  3. Embryotoxicity and teratogenicity studies of an ayurvedic contraceptive--pippaliyadi vati. Chaudhury, M.R., Chandrasekaran, R., Mishra, S. Journal of ethnopharmacology. (2001) [Pubmed]
  4. A comparative study of Embelia schiperi and Embelia keniensis on blood glucose and triglycerides in normal and epinephrine-induced hyperglycemic mice. Kato, A., Miura, T., Nishiyama, Y., Tachibana, Y., Ohnishi, Y., Mathenge, S.G., Albert, R. Am. J. Chin. Med. (1999) [Pubmed]
  5. Non-narcotic orally effective, centrally acting analgesic from an Ayurvedic drug. Atal, C.K., Siddiqui, M.A., Zutshi, U., Amla, V., Johri, R.K., Rao, P.G., Kour, S. Journal of ethnopharmacology. (1984) [Pubmed]
 
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