Anne Oghenekevwe Itemire1 , Enitome Evi Bafor2
1Department of Medical Laboratory Sciences, School of Basic Medical Sciences, College of Medical Sciences, University of Benin; 2Department of Pharmacology and Toxicology, Faculty of Pharmacy, University of Benin, Benin City, Nigeria.For correspondence:- Anne Itemire Email: anne.itemire@uniben.edu Tel:+234-8023315397
Received: 14 July 2024 Accepted: 2 October 2024 Published: 30 October 2024
Citation: Itemire AO, Bafor EE. Uterotrophic bioassay of Carica papaya and Garcinia kola (bi-herbal) aqueous extract. Trop J Pharm Res 2024; 23(10):1677-1683 doi: 10.4314/tjpr.v23i10.12
© 2024 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..
Purpose: To investigate the estrogenic effect of Carica papaya, Garcinia kola, bi-herbal (BH) using the uterotrophic assay. Methods: Twenty-five (25) immature female Wister rats (18 days old) were assigned to 5 groups (A – E). Groups A (control group) and E were treated with 10 mL/kg of distilled water and 10 mg/kg estradiol, respectively, while groups B, C and D were given 10, 100 and 1000 mg/kg BH, respectively by oral gavage for 3 consecutive days. The body weight of the animals and the quantity of feed consumed were determined daily. On the 4th day, the rats were anesthetized and blood was collected for estradiol assay using enzyme-linked immunosorbent assay (ELISA) method. The uteri, ovaries and cervix were dissected and weighed. The organs were fixed in Bouins fluid and processed histologically. Results: The result showed an increase in body weight which corresponded with the quantity of feed consumed. There was a non-significant (p > 0.05), dose-dependent increase in blood estradiol levels in all BH extract-treated groups and a significant (p < 0.05) increase in the estradiol group. Photomicrographs of the uterus, cervix and ovary of all treated groups revealed normal cellular and structural appearance. Conclusion: The aqueous bi-herbal root extract is non-estrogenic at experimental doses. Therefore, it alleviates concerns about infertility and estrogen-induced cancers associated with high estrogen levels with the use of this bi-herbal extract.
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