Consistent ethanol beverage exposure adversely affects male reproductive function
by oxidative stress-related mechanisms. This study was designed to investigate the
spermatogenic and spermiographic effects of myricetin on ethyl-alcohol-induced
sperm toxicity in pre-pubertal male Wistar rats. Thirty-five (35) pre-pubertal male
Wistar rats were divided into seven (7) groups of five (5) rats each. Group 1 was
given distilled water only, group 2 was given 40 % ethanol only, groups 3, 4, and 5
were given 40 % ethanol + 75 mg, 150 mg, and 300 mg myricetin respectively, while
Groups 6 and 7 were given 75 mg and 300 mg myricetin respectively. On completion
of treatment, animals were ketamine sedated and blood was collected through intracardiac
puncture. Epidydimal tissues were eviscerated for spermiography and semen
analysis. Descriptive statistics was used to determine the mean and standard error of
the mean, and One-way analysis of variance was used to determine whether there
were statistically significant differences between the means of independent groups.
Tukey’s post hoc test was used to compare differences among the groups. Tests were
considered statistically significant at p<0.05. Results showed that Sperm motility,
sperm concentration, and the number of normal sperm cells increased in myricetintreated
groups compared to the control and ethanol-induced groups. In conclusion,
these finding suggests that myricetin protected the spermatic cells from oxidative
stress and ameliorated ethanol-based toxicities to the epidydimal sperm cells, hence
promoting its fertility function.
Keywords: Myricetin, Ethyl-alcohol, Semen analysis, Spermiography