bioRxivCell BiologyPreprint
Differential protein expression of GABA A receptor alpha 1 subunit in rat spermatozoa associated with proteomic analysis in testis following methamphetamine administration
S. Nudmamud-Thanoi, P. Kaewman, J. Thongleart, S. Charoenlappanit, S. Roytrakul, S. Thanoi
Abstract
Methamphetamine (METH) can induce spermatogenesis impairment, testicular apoptosis, and abnormal sperm quality. It also promotes changes in the expression of receptors for sex hormones and neurotransmitters, including GABA receptors in the testis. Proteomic assessment focusing on proteins involved in the calcium signalling pathway in the testis can facilitate diagnostic factors contributing to testicular and sperm functions, especially those related to spermatogenesis and fertilisation. In this study, we proposed to determine the localization and differential expression of GABA A receptor alpha 1 subunit (GABA A-1) in the spermatozoa of METH-administrated rats. The differential proteomic profile of the testis was also observed by focusing on proteins in the KEGG pathways belonging to the calcium signalling pathway. There were 212 differentially expressed proteins in the rat testis, based on the cut-off value of 1.2-fold change. Most of those proteins, 13 proteins, were classified in the calcium signalling pathway, including 4 down-regulated and 9 up-regulated proteins. An immunolocalization study of the GABA A-1 receptor revealed its localization in the equatorial segment of the acrosome in the rat spermatozoa, a region involved in acrosome reaction. An increase in GABA A-1 receptor in rat spermatozoa was correlated with an increase in abnormal sperm motility and morphology after methamphetamine exposure. All our findings demonstrate that METH influences intracellular calcium homeostasis by acting through the calcium signalling pathway-associated proteins. Moreover, it might disrupt ion homeostasis in sperm through the GABA A-1 receptor, triggering a change in intracellular calcium and chloride ions. These changes may cause abnormalities in spermatogenesis, testicular apoptosis, and sperm quality impairment.
- organism: rat
- assay: proteomics
- research focus: cell type annotation
- research focus: differential expression
- approach: statistical model
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