Correlation between expression of CatSper family and sperm profiles in the adult mouse testis following Iranian Kerack abuse

• Published in: Andrology (Oxford) Vol. 2; no. 3; pp. 386 - 393
• Main Authors: Amini, M., Shirinbayan, P., Behnam, B., Roghani, M., Farhoudian, A., Joghataei, M. T., Koruji, M.
• Format: Journal Article
• Language: English
• Published: England Wiley Subscription Services, Inc 01-05-2014
• Subjects: Animals; Body Weight - drug effects; Calcium Channels - biosynthesis; Calcium Channels - genetics; CatSper genes; Cell Survival - drug effects; Drug dosages; Epididymis - cytology; illicit substance; Infertility, Male - chemically induced; Iran; Kerack; Male; Mice; Mice, Inbred BALB C; Morphology; Motility; Opium - pharmacology; Rodents; Sperm; Sperm Count; Sperm Motility - drug effects; sperm parameters; Spermatozoa - abnormalities; Spermatozoa - drug effects; Spermatozoa - physiology; Street Drugs - pharmacology; Substance-Related Disorders; testis structure; Iran; CatSper genes; Kerack; testis structure; illicit substance; sperm parameters
• ISSN: 2047-2919; 2047-2927
• DOI: 10.1111/j.2047-2927.2014.00195.x

Summary
Illicit drug use can be an important cause of male infertility. The aim of this study was to investigate the effects of an Iranian illicit drug, Kerack, on sperm parameters, testicular structure and CatSper genes expression of mice. In this study, 25 male mice were divided into five groups consisting of control, sham and three experimental groups. All animal in experimental groups were addicted to Kerack for 7 days. These experimental groups include experimental I which was given Kerack at a dose of 5 mg/kg, experimental II, 35 mg/kg and experimental III, 70 mg/kg, intraperitoneally twice a day for a period of 35 days. Mice were then sacrificed and spermatozoas were removed from cauda epididymis and analyzed for count, motility, morphology (normal/abnormal) and viability. Right testes were removed, weighed and processed for light microscopic studies whereas left testes removed were subjected to total mRNA extraction for using in real‐time PCR (RT‐PCR). The results were analyzed by performing anova (Tukey's tests) and Pearson correlation coefficient. Sperm parameters and seminiferous epithelium thickness were decreased in experimental groups (dose‐dependently) vs. sham and control groups (p < 0.05). RT‐PCR results showed that CatSper 2, 3, 4 genes expressions were reduced with 35 and 70 mg/kg injected Kerack when compared with control testes (p ≤ 0.05). However, CatSper1 expression was only reduced with high dose injected Kerack (70 mg/kg) in comparison to control testes (p ≤ 0.05). This study shows the deleterious effects of Kerack used in Iran on testis structure and sperm parameters in general, and particularly sperm morphology in adult mouse. It could down‐regulate the expression of CatSper genes, resulting in depression of sperm motility.