Abstract

Seventy adult male albino rats were randomly allotted into 3 main groups: control group (n = 10), acute stress-exposed group (n = 30) and chronic stress-exposed group (n = 30). Each of the stressed groups was subdivided into 3 equal subgroups (n = 10/subgroup, SG): subgroup 1 animals were exposed to immobilization stress, SG2 animals, were given immobilization stress and supplemented with α-tocopherol (vitamin E), SG3 animals were exposed to immobilization stress and supplemented with ascorbic acid (vitamin C). Immobilization stress exposure was applied once for 6 continuous hours in the acute stressed group and was 6 hours daily for 10 consecutive days in the chronic stressed group. In all vitamin supplemented groups, both vitamin E and C were administered orally mixed with the diet in a similar dose of 500 mg/kg diet. This supplementation started 6 weeks prior to the stress exposure and continued throughout the experimental period. At the end of the last immobilization session, sera were harvested from all animals thereafter, animals were sacrificed and the testes were immediately excised and processed for further biochemical investigations. Serum testosterone and luteinizing hormone levels were measured and the activities of antioxidant enzymes [catalase (CAT) & glutathione-s-transferase (GST)] as well as malondialdehyde (MDA) concentrations were determined in sera and testes. Compared to control, the results revealed that acute and chronic immobilization stress caused significant decrease in levels of serum testosterone and luteinizing hormone (LH). Also, significant reductions (P < 0.01) were found in the activities of CAT and GST in sera and testes. Contrariwise, there existed a significant (P < 0.05) increase in MDA concentrations in serum and testis. Co-administration of vitamin E or C relatively restored (P < 0.01) the above parameters. Thus, this study draws a conclusion that immobilization stress of male rats significantly inhibited testosterone secretion and induced oxidative stress which partially mediated this inhibition. It also proved a protective role of vitamin E and C against the oxidative stress-induced down-regulation of testosterone secretion with a better efficacy of vitamin E.

Highlights

  • The vast numbers of studies in both humans and animals confirm the inhibitory role of different stressors in the hormonal function of the testis [1]-[3]

  • 3) Chronic stress-exposed group (n = 30) in which animals were subdivided into three subgroups (n = 10/subgroup) as follow; a) Animals were exposed to immobilization stress for 6 hours daily on 10 consecutive days. b) Animals were exposed to immobilization stress and supplemented with vitamin E (500 mg/kg diet). c) Animals were exposed to immobilization stress supplemented with vitamin C (500 mg/kg diet)

  • This finding is consistent with number of studies in humans and animals which confirm the inhibitory role of different stressors on the hormonal function of the testis by decreasing the testosterone level in the blood [2] [3]

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Summary

Introduction

The vast numbers of studies in both humans and animals confirm the inhibitory role of different stressors in the hormonal function of the testis [1]-[3]. A variety of mediating mechanisms have been recenthy suggested [3] [4]. Considerable variations in the response of the hypothalamo-pituitary-gonadal (HPG) axis to stress have been reported. Many stressors decrease LH and testosterone levels by inhibiting luteinizing hormone-releasing hormone (LHRH) synthesis and release from the hypothalamus [1]. There are stimuli that attenuate testosterone levels without altering LH values in both rodents and humans [5]. Testosterone level may be increased at initial stages of acute stress with a constant or even decreased LH level [6]

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