Evidence map›Paper›PMID 40227562›Full record

ArticleCell biochemistry and biophysics2025

Protective Effects of Melatonin and Bee Pollen on Hematotoxicity and Hepatorenal Toxicity Induced by Long-Term Intake of Gabapentin in Female Albino Rats.

Hanan A Okail, Mohamed F El Sayed, Mohamed A Adly, Walaa Magdy Abd Elsamei

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Article in Cell biochemistry and biophysics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Hanan A OkailZoology Department, Faculty of Science, Sohag University, Sohag, Egypt. hananali0441@gmail.com.
Mohamed F El SayedZoology Department, Faculty of Science, Sohag University, Sohag, Egypt.
Mohamed A AdlyZoology Department, Faculty of Science, Sohag University, Sohag, Egypt.
Walaa Magdy Abd ElsameiZoology Department, Faculty of Science, Sohag University, Sohag, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gabapentin (GBN) is an anti-seizure medication that is also used to treat nerve pain and other diseases. However, its misuse is currently a growing worry, as it may pose a significant health danger. The present study aimed to evaluate the protective effect of melatonin (MEL) and bee pollen (BP) as antioxidants against GBN-induced hematotoxicity and hepatorenal toxicity in female Albino rats. In this study, fifty-six adult female albino rats were divided into seven groups (n = 8 each), served as control, GBN, MEL, BP, MEL + GBN, BP + GBN, and MEL + BP + GBN treated groups. Results showed that oral administration of GBN resulted in a hematological toxicity as confirmed by a significant reduction in RBCs, Hb concentration, Ht%, MCV, MCH, platelets as well as altering of leukocyte profiles, WBCs, neutrophils, lymphocytes, monocytes, eosinophils and basophils. The biochemical results of liver and kidney functions showed a significant decrease in serum glucose, total protein, triglycerides, urea and uric acid. However, a significant increase in albumin, cholesterol, creatinine as well as ALP, AST, and ALT liver enzymes compared to the control was found. The oral administration of MEL and BP 12 h before GBN mostly ameliorates the altered hematological and biochemical parameters as well as hepatic and renal histopathological architecture to normal levels. In conclusion, Pre-treatment with MEL and BP, individually or together provided protection against the GBN induced changes in the blood parameters as well as hepatorenal structure and function.

Indexed as

AminesCyclohexanecarboxylic Acidsgamma-Aminobutyric AcidKidneyLiverMelatoninPollenProtective AgentsAdministration, OralAnimalsAntioxidantsBeesFemaleGabapentinRatsAminesAntioxidantsCyclohexanecarboxylic AcidsGabapentingamma-Aminobutyric AcidMelatoninProtective AgentsBee pollenGabapentinKidney functionLiver enzymesMelatonin

Identifiers

PMID40227562

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.