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American Journal of Biochemistry and Molecular Biology
  Year: 2011 | Volume: 1 | Issue: 1 | Page No.: 95-100
DOI: 10.3923/ajbmb.2011.95.100
Effect of Angiotensin I-Converting Enzyme Inhibitor, Captopril, on Body Weight and Food and Water Consumption in Oral Contraceptive-Treated Rats
Akhigbe R. Eghoghosoa, Olatunji L. Aderemi, Soladoye A. Olufemi and Oyeyipo I. Peter

Abstract:
Studies have shown that hormonal changes that occur during menstrual or oestrous cycle influence angiotensin-induced water intake. However, little is known about the effects of Oral Contraceptive (OC) on body weight and eating habit when Renin-Angiotensin System (RAS) is suppressed. This study documents the effect of OC on weight gain and food and water consumption. It also assesses whether suppression of RAS by captopril would affect OC-induced changes. Forty female rats, distributed into 4 groups (10 rats in each), were used for the experiment. Vehicles-treated, OC-treated, captopril-treated and OC+captopril-treated groups. The OC used contained 1.0 μg ethinyloestradiol and 10.0 μg norgestrel. Body weight, food and water intake were recorded daily throughout the experiment period. Food and water consumed per day per 100 g body weight was also calculated. The OC-treated and OC+captopril-treated rats had significantly lower body weight when compared with those of vehicle treated and captopril-treated rats. The OC-treated rats consumed significantly less food than vehicle-treated and captopril-treated groups. OC+captopril-treated rats consumed significantly less food than other groups. The OC administration is associated with reduction in weight gain and food and water consumption. Co-administration of captopril significantly augments this effect.
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How to cite this article:

Akhigbe R. Eghoghosoa, Olatunji L. Aderemi, Soladoye A. Olufemi and Oyeyipo I. Peter, 2011. Effect of Angiotensin I-Converting Enzyme Inhibitor, Captopril, on Body Weight and Food and Water Consumption in Oral Contraceptive-Treated Rats. American Journal of Biochemistry and Molecular Biology, 1: 95-100.

DOI: 10.3923/ajbmb.2011.95.100

URL: https://scialert.net/abstract/?doi=ajbmb.2011.95.100

 
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