Casein and pea enriched high-protein diet attenuates arsenic provoked apoptosis in testicles of adult rats.

IF 2.2 4区 医学 Q3 TOXICOLOGY Toxicology Research Pub Date : 2023-06-14 eCollection Date: 2023-08-01 DOI:10.1093/toxres/tfad043
Sagnik Biswas, Priyankar Pal, Rubia Mondal, Prabir Kumar Mukhopadhyay
{"title":"Casein and pea enriched high-protein diet attenuates arsenic provoked apoptosis in testicles of adult rats.","authors":"Sagnik Biswas, Priyankar Pal, Rubia Mondal, Prabir Kumar Mukhopadhyay","doi":"10.1093/toxres/tfad043","DOIUrl":null,"url":null,"abstract":"<p><p>Arsenic toxicity is a major health issue that also threats male reproductive system leading to impairment of fertility. The antioxidant capacity of casein and pea enriched formulated high-protein diet (FHPD) is found to be effective in different toxicity management. The present study was endeavored to investigate the mitigatory aspect of FHPD on arsenic stimulated testicular apoptosis. Adult male rats were maintained on either normal diet as control (Gr I, <i>n</i> = 8) and arsenic (As<sub>2</sub>O<sub>3</sub>) treated at a dose of 3 mg/kg/rat/day (Gr II, <i>n</i> = 8) or on isocaloric FHPD as supplemented (Gr III, <i>n</i> = 8) with same dose of arsenic for 30 consecutive days. Testicular histomorphometry, spermatokinetics, testicular functional marker enzymes, serum gonadotrophins, oxidative stress markers, testicular deoxyribonucleic acid (DNA) damage, and apoptosis markers were evaluated to assess the reprotoxicity of arsenic and subsequent protection by FHPD. FHPD protected the histopathological alterations and also restored normal spermatogenesis. Altered enzymatic activities of testicular functional markers like lactate dehydrogenase, γ-glutamyl transferase, acid phosphatase, and alkaline phosphatase were also regularized. FHPD also reinstated the normal level of follicle stimulating hormone (FSH), luteinising hormone (LH), and also normalized the enzymatic activities of testicular glutathione peroxidase and glutathione reductase. Testicular DNA damage was also prevented by FHPD supplementation. Testicular apoptosis marked by the altered messenger ribonucleic acid and protein expression of apoptotic markers like Bax, Bcl-2, caspase 9, and caspase 3 were also attenuated upon FHPD supplementation along with diminution of arsenic accumulation in testicular tissues. FHPD not only mitigated the adverse effects of arsenic induced gonadotoxicity but also helped in sustaining the normal reproductive functions.</p>","PeriodicalId":105,"journal":{"name":"Toxicology Research","volume":"12 4","pages":"551-563"},"PeriodicalIF":2.2000,"publicationDate":"2023-06-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10470344/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Toxicology Research","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1093/toxres/tfad043","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/8/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"TOXICOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Arsenic toxicity is a major health issue that also threats male reproductive system leading to impairment of fertility. The antioxidant capacity of casein and pea enriched formulated high-protein diet (FHPD) is found to be effective in different toxicity management. The present study was endeavored to investigate the mitigatory aspect of FHPD on arsenic stimulated testicular apoptosis. Adult male rats were maintained on either normal diet as control (Gr I, n = 8) and arsenic (As2O3) treated at a dose of 3 mg/kg/rat/day (Gr II, n = 8) or on isocaloric FHPD as supplemented (Gr III, n = 8) with same dose of arsenic for 30 consecutive days. Testicular histomorphometry, spermatokinetics, testicular functional marker enzymes, serum gonadotrophins, oxidative stress markers, testicular deoxyribonucleic acid (DNA) damage, and apoptosis markers were evaluated to assess the reprotoxicity of arsenic and subsequent protection by FHPD. FHPD protected the histopathological alterations and also restored normal spermatogenesis. Altered enzymatic activities of testicular functional markers like lactate dehydrogenase, γ-glutamyl transferase, acid phosphatase, and alkaline phosphatase were also regularized. FHPD also reinstated the normal level of follicle stimulating hormone (FSH), luteinising hormone (LH), and also normalized the enzymatic activities of testicular glutathione peroxidase and glutathione reductase. Testicular DNA damage was also prevented by FHPD supplementation. Testicular apoptosis marked by the altered messenger ribonucleic acid and protein expression of apoptotic markers like Bax, Bcl-2, caspase 9, and caspase 3 were also attenuated upon FHPD supplementation along with diminution of arsenic accumulation in testicular tissues. FHPD not only mitigated the adverse effects of arsenic induced gonadotoxicity but also helped in sustaining the normal reproductive functions.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
富含酪蛋白和豌豆的高蛋白饮食可减轻砷引起的成年大鼠睾丸凋亡。
砷中毒是一个重大的健康问题,也威胁着男性生殖系统,导致生育能力受损。研究发现,富含酪蛋白和豌豆的配方高蛋白日粮(FHPD)的抗氧化能力在不同的毒性处理中都很有效。本研究旨在探讨 FHPD 对砷刺激睾丸凋亡的缓解作用。成年雄性大鼠以正常饮食作为对照(Gr I,n = 8),并以 3 毫克/千克/大鼠/天的剂量服用砷(As2O3)(Gr II,n = 8),或连续 30 天服用补充相同剂量砷的等热量 FHPD(Gr III,n = 8)。对睾丸组织形态学、精子动力学、睾丸功能标志酶、血清促性腺激素、氧化应激标志物、睾丸脱氧核糖核酸(DNA)损伤和细胞凋亡标志物进行了评估,以评估砷的再毒性和 FHPD 的后续保护作用。FHPD 保护了组织病理学改变,并恢复了正常的精子发生。乳酸脱氢酶、γ-谷氨酰转移酶、酸性磷酸酶和碱性磷酸酶等睾丸功能标志物的酶活性改变也得到了恢复。FHPD 还能恢复促卵泡激素(FSH)和黄体生成素(LH)的正常水平,并使睾丸谷胱甘肽过氧化物酶和谷胱甘肽还原酶的酶活性恢复正常。补充 FHPD 还能防止睾丸 DNA 损伤。补充 FHPD 后,以 Bax、Bcl-2、caspase 9 和 caspase 3 等凋亡标志物的信使核糖核酸和蛋白质表达改变为标志的睾丸凋亡也得到了缓解,同时睾丸组织中的砷积累也减少了。FHPD 不仅减轻了砷诱导的性腺毒性的不良影响,还有助于维持正常的生殖功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Toxicology Research
Toxicology Research TOXICOLOGY-
CiteScore
3.60
自引率
0.00%
发文量
82
期刊介绍: A multi-disciplinary journal covering the best research in both fundamental and applied aspects of toxicology
期刊最新文献
Unveiling the interspecies correlation and sensitivity factor analysis of rat and mouse acute oral toxicity of antimicrobial agents: first QSTR and QTTR Modeling report. Stress survival and longevity of Caenorhabditis elegans lacking NCS-1. Lipid-core nanocapsules containing simvastatin do not affect the biochemical and hematological indicators of toxicity in rats. Proteomics reveals that nanoplastics with different sizes induce hepatocyte apoptosis in mice through distinct mechanisms involving mitophagy dysregulation and cell cycle arrest. Antibiotic contaminants and their impact in Gingee River, Puducherry: insights from SPE-UPLC-MS/MS and zebrafish study.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1