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Authors
Affiliations
1 Department of Biochemistry, Kakatiya University, Warangal (A.P.), IN
2 Department of Zoology, University College, Kakatiya University, Warangal (A.P.), IN
3 University College of Pharmaceutical Sciences, Kakatiya University, Warangal (A.P.), IN
Source
Asian Journal of Bio Science, Vol 4, No 2 (2010), Pagination: 162-165
Abstract
Progesterone is important for initiation and maintenance of pregnancy (hormone of pregnancy).The discovery that in the absence of progesterone, pregnancy cannot be initiated or maintained provided the basis for a massive effort of synthesis of antiprogestin molecules to develop emergency contraceptive pills. By the consequences, till date few progesterone antagonists (antiprogestins) have been synthesized which bind to and block the progesterone receptor. However, none of the antiprogestins are “pure” antiprogestins, having marked antiglucocorticoid properties as well, especially at higher doses. Thus the search for the “ideal” progesterone antagonist continues. The main objective of the present work is to evaluate antiprogestin activity of progesterone analogue, 14 β- hydroxy progesterone. A pregnane glycoside, carumbelloside-I (3-O-beta-D-glucopyranosyl-(1→6)-beta-Dglucopyranosyl- 3beta,14beta-dihydroxypregn-5-en-20-one) was isolated from the n-butanolic extract of Caralluma umbellata (Asclepiadaceae) and was modified to a structural analog of progesterone, 14 β- Hydroxy progesterone (14β- OHP) in just two simple steps. Anti-implantation and abortifacient activities of the compound have been studied to evaluate its antiprogestin activity. To study the anti-implantation effect, pregnant wistar strain albino rats were administered with 14β-OHP (daily dose of 5 mg/Kg body weight) intraperitoneally from the day 1to day 7 of pregnancy. On day 10, laparotomy was performed under light ether anesthesia. The uteri were examined to determine the number of implantation sites. The abdomens were sutured and the animals were allowed to go on term. The number of young born at term was also recorded. The abortifacient activity was studied in another group of pregnant rats. The animals were treated with 14β- OHP (5 mg/Kg body weight daily) intraperitoneally from day 8 to 12of pregnancy. They were sacrificed on day 19 of pregnancy. Both horns of uterus were observed for the number of live fetuses. The compound showed about 44.23% anti-implantation and 62% of abortifacient effect at their corresponding dose levels tested. The results indicated the antiprogestin activity of 14 β- hydroxy progesterone in albino rats.
Keywords
14β- OHP, Anti-Implantation, Abortifacient, Antiprogestin and Contraceptive.
