Maternal malnutrition induces inflammatory pathways and oxidative stress in the dorsolateral prostate of male offspring rats.

IF 4.4 4区 医学 Q1 GERIATRICS & GERONTOLOGY
Renato Mattos, Matheus Naia Fioretto, Sérgio Alexandre Alcantara Dos Santos, Isabelle Tenori Ribeiro, Maycon Tavares Emílio-Silva, Luiz Marcos Frediani Portela, Clélia Akiko Hiruma Lima, Fabio Rodrigues Ferreira Seiva, Luis A Justulin
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Abstract

Maternal conditions during pregnancy can influence the long-term health of offspring. In particular, maternal malnutrition (MM), such as protein restriction, affects the development of several organs, including the male reproductive system. This study examined how a low-protein maternal diet impacts the structure and function of the dorsolateral prostate (DLP) in aging male rats. Male offspring were divided into two groups: A control group (CTR), whose mothers received a normal protein diet (17%) during pregnancy and lactation, and a low-protein group (GLLP), whose mothers received a low-protein diet (6%) during the same period. At 540 days of age, the offspring were euthanized, and the DLPs were collected for analysis. The GLLP group showed significant structural changes in the DLP, including increased epithelial and reduced stromal compartments. These rats also had lower levels of probasin (a prostate-specific protein), along with a higher number of mast cells, CD68 + macrophages, and IL-10 protein expression, indicating inflammation. Antioxidant balance was disrupted: Glutathione (GSH) levels increased, while catalase (CAT) and superoxide dismutase (SOD) decreased. The expression of SIRT1, a protein linked to aging and oxidative stress control, was reduced. In silico analysis using human prostate cancer data (PRAD-TCGA) revealed that biological pathways related to oxidative stress, immune response, and tissue remodeling were disrupted in both the rat model and human prostate cancer. In summary, maternal protein restriction leads to long-term changes in the dorsolateral prostate of aging male offspring, including inflammation, oxidative stress, and tissue remodeling. The reduced expression of SIRT1 may play a key role in these effects.

母体营养不良诱导雄性后代大鼠前列腺背外侧炎症通路和氧化应激。
怀孕期间的母亲状况会影响后代的长期健康。特别是,产妇营养不良(MM),如蛋白质限制,影响几个器官的发育,包括男性生殖系统。本研究探讨了低蛋白母性饮食如何影响衰老雄性大鼠背外侧前列腺(DLP)的结构和功能。雄性后代被分为两组:对照组(CTR),其母亲在怀孕和哺乳期间接受正常蛋白质饮食(17%);低蛋白组(GLLP),其母亲在同一时期接受低蛋白饮食(6%)。在540日龄时,对后代实施安乐死,并收集dlp进行分析。GLLP组DLP结构发生显著变化,包括上皮细胞增多和间质室减少。这些大鼠也有较低水平的probasin(前列腺特异性蛋白),以及大量肥大细胞,CD68 +巨噬细胞和IL-10蛋白表达,表明炎症。抗氧化平衡被破坏:谷胱甘肽(GSH)水平升高,过氧化氢酶(CAT)和超氧化物歧化酶(SOD)降低。SIRT1(一种与衰老和氧化应激控制有关的蛋白质)的表达减少。利用人类前列腺癌数据(PRAD-TCGA)进行的计算机分析显示,在大鼠模型和人类前列腺癌中,与氧化应激、免疫反应和组织重塑相关的生物通路都被破坏。综上所述,母体蛋白限制导致衰老雄性后代前列腺背外侧的长期变化,包括炎症、氧化应激和组织重塑。SIRT1的表达降低可能在这些作用中起关键作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Biogerontology
Biogerontology 医学-老年医学
CiteScore
8.00
自引率
4.40%
发文量
54
审稿时长
>12 weeks
期刊介绍: The journal Biogerontology offers a platform for research which aims primarily at achieving healthy old age accompanied by improved longevity. The focus is on efforts to understand, prevent, cure or minimize age-related impairments. Biogerontology provides a peer-reviewed forum for publishing original research data, new ideas and discussions on modulating the aging process by physical, chemical and biological means, including transgenic and knockout organisms; cell culture systems to develop new approaches and health care products for maintaining or recovering the lost biochemical functions; immunology, autoimmunity and infection in aging; vertebrates, invertebrates, micro-organisms and plants for experimental studies on genetic determinants of aging and longevity; biodemography and theoretical models linking aging and survival kinetics.
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