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1.
Pakistan Journal of Pharmaceutical Sciences. 2018; 31 (3 Supp.): 997-1001
in English | IMEMR | ID: emr-198709

ABSTRACT

To examine the action mechanism that mediates the anti-fertility effect of Costus speciosus extract, research was conducted on male Sprague-Dawley rats. Costus extract was given to male rats for 14 days at various doses, namely 275, 550 and 1,100 mg kg-1 day-1 in 0.5% sodium CMC. The results showed that Costus extract with doses ranging from 275 to 1,100 mg kg-1 day-1 was able to inhibit pregnancy among female rats by 10-70%. No obstacles in terms of sexual behavior were identified among male rats. The anti-fertility effect of Costus extract kicked in without involving a decreased level of male reproductive hormones

2.
Asian Pacific Journal of Tropical Medicine ; (12): 438-442, 2013.
Article in English | WPRIM | ID: wpr-820025

ABSTRACT

OBJECTIVE@#To investigate the hepatoprotective and antioxidant activity of pentagamavunon-0(PGV-0) against CCl4-induced hepatic injury in rats.@*METHODS@#The groups of animals were administered with PGV-0 at the doses 2.5, 5, 10, and 20 mg/kg b.w., p.o. once in a day for 6 days and at day 7 the animals were administrated with carbon tetrachloride (CCl) (20%, 2 mL/kg b.w. in liquid paraffin (i.p.). The effect of PGV-0 on serum transaminase (SGPT), alkaline phosphates (ALP) and total bilirubin were determined in CCl4-induced hepatotoxicity in rats. Further, the effects of PGV-0 on glutathione (GSH) content, catalase (CAT) and NO free radical scavenging activity also were investigated.@*RESULTS@#The results demonstrated that PGV-0 significantly reduced the activity of SGPT, serum ALP and total bilirubin in CCl4 induced rat hepatotoxicity. PGV-0 has effect on the antioxidant and free radical defense system. It prevented the depletion level of GSH and decrease activity of CAT in CCl4-induced liver injury in rats. PGV-0 also demonstrated the free radical scavenger effects on NO free radical scavenging activity with ES value of 32.32 μM.@*CONCLUSION@#All of our findings suggests that PGV-0 could protect the liver cells from CCl4-induced liver damages and the mechanism may through the antioxidative effect of PGV-0 to prevent the accumulation of free radicals and protect the liver damage.


Subject(s)
Animals , Male , Rats , Analysis of Variance , Antioxidants , Pharmacology , Carbon Tetrachloride Poisoning , Drug Therapy , Metabolism , Catalase , Metabolism , Chemical and Drug Induced Liver Injury , Drug Therapy , Metabolism , Curcumin , Pharmacology , Glutathione , Metabolism , Nitric Oxide , Metabolism , Rats, Wistar
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