Spaceflight experiments carried out in microgravity environments have revealed that exposure to altered gravity condition results in alteration of several cellular functions and, consequently, of several apparatuses. There is some evidence in the literature indicating that spaceflight affects the physiology of the testis. The data on effects of spaceflight or simulated microgravity on testicular function, however, sometimes appear contradictory. In the present study we used an in vitro experimental model in order to investigate the direct effects of microgravity on testicular tissue. We generated a microgravity environment using the Rotating Wall Vessel and performed experiments on testicular fragments isolated from pre-pubertal rats. In this model we then analyzed several parameters such as histological integrity, cell proliferation, cell apoptosis, occludin distribution pattern, and hormonal secretions. The emerging picture shows some alterations of testicular tissue physiology. Interestingly, we also demonstrate for the first time that, in organ culture, Leydig cell survival is severely affected by simulated microgravity.
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Reprod Sci
July 2024
Stem Cell Research Center, Golestan University of Medical Sciences, Gorgan, 4934174515, Iran.
Gravity in space can have a negative impact on the reproductive system. Given that the reproductive system is one of vitamin D's objectives, this study will use a simulated microgravity model to evaluate its impact on the rat reproductive system.Twenty-two male Wistar rats were allocated into four groups at random.
View Article and Find Full Text PDFFront Physiol
August 2022
College of Medicine, Mohammed Bin Rashid University of Medicine and Health Sciences, Dubai, United Arab Emirates.
With the advancement in space exploration and the intention to establish an inhabitable human settlement on Mars, it is important to investigate the effects of exposure to space/microgravity and the associated radiations on procreation. Sperm function and integrity are fundamental to male reproduction and can potentially be affected by the environmental changes experienced in space. Therefore, this study was conducted to systematically gather, filter, and collate all the relevant information on the effects of spaceflight on male reproductive parameters and functions.
View Article and Find Full Text PDFReprod Biol Endocrinol
March 2021
Department of Physiology, Faculty of Veterinary Medicine, Zagazig University, Zagazig, 44519, Egypt.
Background: Spaceflights-induced microgravity can alter various physiological processes in human's body including the functional status of the reproductive system. Rodent model of tail-suspension hindlimb unloading is extensively used to stimulate the organs responses to the microgravity condition. This study explores the potential effects of hindlimb unloading on testicular functions and spermatogenesis in adult male rats and the underlying mechanism/s.
View Article and Find Full Text PDFNat Rev Endocrinol
December 2019
Center for Occupational and Environmental Health, Department of Medicine, Department of Developmental and Cell Biology, Program in Public Health, University of California Irvine, Irvine, CA, USA.
Extended travel in deep space poses potential hazards to the reproductive function of female and male astronauts, including exposure to cosmic radiation, microgravity, increased gravity (hypergravity), psychological stress, physical stress and circadian rhythm disruptions. This Review focuses on the effects of microgravity, hypergravity and cosmic radiation. Cosmic radiation contains protons, helium nuclei and high charge and energy (HZE) particles.
View Article and Find Full Text PDFSci Rep
June 2017
Department of Biomedicine and Prevention, University of Rome Tor Vergata, 00133, Rome, Italy.
Cytochrome P450-aromatase catalyzes estrogen biosynthesis from C steroids. In the testis, Sertoli cells express P450-aromatase and represent the primary source of estrogen during prepuberal age. This study focused on the effect of simulated microgravity (SM) on aromatase expression in primary mouse Sertoli cells.
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