» Articles » PMID: 35903144

Does Orexin B-Binding Receptor 2 for Orexins Regulate Testicular and Epididymal Functions in Normal and Cryptorchid Dogs?

Overview
Journal Front Vet Sci
Date 2022 Jul 29
PMID 35903144
Authors
Affiliations
Soon will be listed here.
Abstract

Orexins A (OXA) and B (OXB) and the receptors 1 (OX1R) and 2 (OX2R) for orexins are hypothalamic peptides found in several mammalian organs and participated to the control of a wide assortment of physiological and pathological functions. The distribution of OXA and OX1R has been extensively studied in the male gonad of mammals. Here, we examined the expression and localization of OXB and OX2R as well as their possible involvement in the regulation of testicular and epididymal functions, in healthy and cryptorchid dogs, employing some techniques such as immunohistochemistry, Western blotting, and real-time RT-PCR. In were also carried out for evaluating the steroidogenic effect of OXB. OXB and OX2R were expressed in spermatocytes, spermatids, and Leydig cells in normal testis. Their localization was restricted to Sertoli and Leydig cells in cryptorchid conditions. OXB was found to be localized in all tracts of both normal and cryptorchid epididymis, whereas OX2R was found only in the caput. Because the small molecular weight of the peptides OXA and OXB, the expression of their precursor prepro-orexin (), , and proteins and mRNAs were investigated by means of Western blot and real-time RT-PCR analyses, respectively, in all tested groups of. In particular, the mRNA level expression of all three genes was higher in cryptorchid dogs than in normal ones. In demonstrated that OXB-by binding OX2R-is not involved in testicular steroidogenic processes. Therefore, the findings of this study might be the basis for further functional and molecular studies addressing the possible biochemical effects of OXB and OX2R in normal and pathological conditions of the male reproductive system.

Citing Articles

A Comparative Analysis of Orexins in the Physio-Pathological Processes of the Male Genital Tract: New Challenges? A Review.

Costagliola A, Montano L, Langella E, Lombardi R, Squillacioti C, Mirabella N Vet Sci. 2024; 11(3).

PMID: 38535865 PMC: 10975741. DOI: 10.3390/vetsci11030131.


Orexins and Prostate Cancer: State of the Art and Potential Experimental and Therapeutic Perspectives.

Costagliola A, Lombardi R, Liguori G, Morrione A, Giordano A Cancer Genomics Proteomics. 2023; 20(6suppl):637-645.

PMID: 38035703 PMC: 10687730. DOI: 10.21873/cgp.20412.

References
1.
Lephart E . A review of brain aromatase cytochrome P450. Brain Res Brain Res Rev. 1996; 22(1):1-26. View

2.
Wei Y, Zhou Y, Tang X, Liu B, Shen L, Long C . Testicular developmental impairment caused by flutamide-induced and DEHP-induced cryptorchid rat models is mediated by excessive apoptosis and deficient autophagy. Toxicol Mech Methods. 2018; 28(7):507-519. DOI: 10.1080/15376516.2018.1459994. View

3.
Assisi L, Tafuri S, Liguori G, Paino S, Pavone L, Staiano N . Expression and role of receptor 1 for orexins in seminiferous tubules of rat testis. Cell Tissue Res. 2012; 348(3):601-7. DOI: 10.1007/s00441-012-1394-8. View

4.
De Luca A, Liguori G, Squillacioti C, Paino S, Germano G, Ali S . Expression of urocortin and its receptors in the rat epididymis. Reprod Biol. 2014; 14(2):140-7. DOI: 10.1016/j.repbio.2014.01.007. View

5.
Rouet-Benzineb P, Rouyer-Fessard C, Jarry A, Avondo V, Pouzet C, Yanagisawa M . Orexins acting at native OX(1) receptor in colon cancer and neuroblastoma cells or at recombinant OX(1) receptor suppress cell growth by inducing apoptosis. J Biol Chem. 2004; 279(44):45875-86. DOI: 10.1074/jbc.M404136200. View