Chronic restraint stress induces sperm acrosome reaction and changes in testicular tyrosine phosphorylated proteins in rats

Background: Stress is a cause of male infertility. Although sex hormones and sperm quality have been shown to be low in stress, sperm physiology and testicular functional proteins, such as phosphotyrosine proteins, have not been documented. Objective: To investigate the acrosome status and alteratio...

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Main Authors: Supatcharee Arun (Author), Jaturon Burawat (Author), Wannisa Sukhorum (Author), Apichakan Sampannang (Author), Chanwit Maneenin (Author), Sitthichai Iamsaard (Author)
Format: Book
Published: Shahid Sadoughi University of Medical Science, Yazd, Iran, 2016-07-01T00:00:00Z.
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001 doaj_8b4d668756c84d7fbfa9952dff5a2ad6
042 |a dc 
100 1 0 |a Supatcharee Arun  |e author 
700 1 0 |a Jaturon Burawat  |e author 
700 1 0 |a Wannisa Sukhorum  |e author 
700 1 0 |a Apichakan Sampannang  |e author 
700 1 0 |a Chanwit Maneenin  |e author 
700 1 0 |a Sitthichai Iamsaard  |e author 
245 0 0 |a Chronic restraint stress induces sperm acrosome reaction and changes in testicular tyrosine phosphorylated proteins in rats 
260 |b Shahid Sadoughi University of Medical Science, Yazd, Iran,   |c 2016-07-01T00:00:00Z. 
500 |a 1680-6433 
500 |a 2008-2177 
520 |a Background: Stress is a cause of male infertility. Although sex hormones and sperm quality have been shown to be low in stress, sperm physiology and testicular functional proteins, such as phosphotyrosine proteins, have not been documented. Objective: To investigate the acrosome status and alterations of testicular proteins involved in spermatogenesis and testosterone synthesis in chronic stress in rats. Materials and Methods: In this experimental study, male rats were divided into 2 groups (control and chronic stress (CS), n=7). CS rats were immobilized (4 hr/day) for 42 consecutive days. The blood glucose level (BGL), corticosterone, testosterone, acrosome status, and histopathology were examined. The expressions of testicular steroidogenic acute regulatory (StAR), cytochrome P450 side chain cleavage (CYP11A1), and phosphorylated proteins were analyzed. Results: Results showed that BGL (71.25±2.22 vs. 95.60±3.36 mg/dl), corticosterone level (24.33±4.23 vs. 36.9±2.01 ng/ml), acrosome reacted sperm (3.25±1.55 vs. 17.71±5.03%), and sperm head abnormality (3.29±0.71 vs. 6.21±1.18%) were significantly higher in CS group in comparison with control. In contrast, seminal vesicle (0.41±0.05 vs. 0.24±0.07 g/100g), testosterone level (3.37±0.79 vs. 0.61±0.29 ng/ml), and sperm concentration (115.33±7.70 vs. 79.13±3.65×106 cells/ml) of CS were significantly lower (p<0.05) than controls. Some atrophic seminiferous tubules and low sperm mass were apparent in CS rats. The expression of CYP11A1 except StAR protein was markedly decreased in CS rats. In contrast, a 55 kDa phosphorylated protein was higher in CS testes. Conclusion: CS decreased the expression of CYP11A, resulting in decreased testosterone, and increased acrosome-reacted sperm, assumed to be the result of an increase of 55 kDa phosphorylated protein. 
546 |a EN 
690 |a Gynecology and obstetrics 
690 |a RG1-991 
690 |a Reproduction 
690 |a QH471-489 
655 7 |a article  |2 local 
786 0 |n Iranian Journal of Reproductive Medicine, Vol 14, Iss 7, Pp 443-452 (2016) 
787 0 |n http://www.ssu.ac.ir/ijrm/index.php/ijrm/article/view/2013/1000 
787 0 |n https://doaj.org/toc/1680-6433 
787 0 |n https://doaj.org/toc/2008-2177 
856 4 1 |u https://doaj.org/article/8b4d668756c84d7fbfa9952dff5a2ad6  |z Connect to this object online.