现实世界中衰老与微粒物质 2.5 暴露的交集:对大鼠炎症和内分泌轴活动的影响。

IF 2.3 4区 医学 Q3 ENDOCRINOLOGY & METABOLISM
International Journal of Endocrinology Pub Date : 2024-06-27 eCollection Date: 2024-01-01 DOI:10.1155/2024/8501696
Cuiying Liu, Jian Yang, Longfei Guan, Liwei Jing, Shuqin Xiao, Liu Sun, Baohui Xu, Heng Zhao
{"title":"现实世界中衰老与微粒物质 2.5 暴露的交集:对大鼠炎症和内分泌轴活动的影响。","authors":"Cuiying Liu, Jian Yang, Longfei Guan, Liwei Jing, Shuqin Xiao, Liu Sun, Baohui Xu, Heng Zhao","doi":"10.1155/2024/8501696","DOIUrl":null,"url":null,"abstract":"<p><p>Exposure to particulate matter 2.5 (PM2.5) is detrimental to multiple organ systems. Given the factor that aging also alters the cellularity and response of immune system and dysfunction of hypothalamic-pituitary-adrenal, -gonad and -thyroid axes, it is imperative to investigate whether chronic exposure to PM2.5 interacts with aging in these aspects. In this study, two-months-old Sprague-Dawley rats were exposed to real world PM2.5 for 16 months. PM2.5 exposure diminished the relative numbers of CD4<sup>+</sup> T cells and CD8<sup>+</sup> T cells and increased the relative number of B cells in the peripheral blood of male rats. Conversely, only reduced relative number of CD4<sup>+</sup> T cells was seen in the blood of female rats. These shifts resulted in elevated levels of proinflammatory factors interleukin-6 and tumor necrosis factor-<i>α</i> in the circulatory systems of both sex, with females also evidencing a rise in interleukin-1<i>β</i> levels. Moreover, heightened interleukin-6 was solely discernible in the hippocampus of female subjects, while increased tumor necrosis factor-<i>α</i> concentrations were widespread in female brain regions but confined to the male hypothalamus. Notable hormonal decreases were observed following PM2.5 exposure in both sex. These comprised declines in biomolecules such as corticotrophin-releasing hormone and cortisol, generated by the hypothalamic-pituitary-adrenal axis, and thyroid-releasing hormone and triiodothyronine, produced by the hypothalamic-pituitary-thyroid axis. Hormonal elements such as gonadotropin-releasing hormone, luteinizing hormone, and follicle-stimulating hormone, derived from the hypothalamic-pituitary-gonad axis, were also diminished. Exclusive to male rats was a reduction in adrenocorticotropic hormone levels, whereas a fall in thyroid-stimulating hormone was unique to female rats. Decreases in sex-specific hormones, including testosterone, estradiol, and progesterone, were also noted. These findings significantly enrich our comprehension of the potential long-term health repercussions associated with PM2.5 interaction particularly among the aging populace.</p>","PeriodicalId":13966,"journal":{"name":"International Journal of Endocrinology","volume":null,"pages":null},"PeriodicalIF":2.3000,"publicationDate":"2024-06-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11223905/pdf/","citationCount":"0","resultStr":"{\"title\":\"Intersection of Aging and Particulate Matter 2.5 Exposure in Real World: Effects on Inflammation and Endocrine Axis Activities in Rats.\",\"authors\":\"Cuiying Liu, Jian Yang, Longfei Guan, Liwei Jing, Shuqin Xiao, Liu Sun, Baohui Xu, Heng Zhao\",\"doi\":\"10.1155/2024/8501696\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Exposure to particulate matter 2.5 (PM2.5) is detrimental to multiple organ systems. Given the factor that aging also alters the cellularity and response of immune system and dysfunction of hypothalamic-pituitary-adrenal, -gonad and -thyroid axes, it is imperative to investigate whether chronic exposure to PM2.5 interacts with aging in these aspects. In this study, two-months-old Sprague-Dawley rats were exposed to real world PM2.5 for 16 months. PM2.5 exposure diminished the relative numbers of CD4<sup>+</sup> T cells and CD8<sup>+</sup> T cells and increased the relative number of B cells in the peripheral blood of male rats. Conversely, only reduced relative number of CD4<sup>+</sup> T cells was seen in the blood of female rats. These shifts resulted in elevated levels of proinflammatory factors interleukin-6 and tumor necrosis factor-<i>α</i> in the circulatory systems of both sex, with females also evidencing a rise in interleukin-1<i>β</i> levels. Moreover, heightened interleukin-6 was solely discernible in the hippocampus of female subjects, while increased tumor necrosis factor-<i>α</i> concentrations were widespread in female brain regions but confined to the male hypothalamus. Notable hormonal decreases were observed following PM2.5 exposure in both sex. These comprised declines in biomolecules such as corticotrophin-releasing hormone and cortisol, generated by the hypothalamic-pituitary-adrenal axis, and thyroid-releasing hormone and triiodothyronine, produced by the hypothalamic-pituitary-thyroid axis. Hormonal elements such as gonadotropin-releasing hormone, luteinizing hormone, and follicle-stimulating hormone, derived from the hypothalamic-pituitary-gonad axis, were also diminished. Exclusive to male rats was a reduction in adrenocorticotropic hormone levels, whereas a fall in thyroid-stimulating hormone was unique to female rats. Decreases in sex-specific hormones, including testosterone, estradiol, and progesterone, were also noted. These findings significantly enrich our comprehension of the potential long-term health repercussions associated with PM2.5 interaction particularly among the aging populace.</p>\",\"PeriodicalId\":13966,\"journal\":{\"name\":\"International Journal of Endocrinology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":2.3000,\"publicationDate\":\"2024-06-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11223905/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Journal of Endocrinology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1155/2024/8501696\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q3\",\"JCRName\":\"ENDOCRINOLOGY & METABOLISM\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Endocrinology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1155/2024/8501696","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/1/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"ENDOCRINOLOGY & METABOLISM","Score":null,"Total":0}
引用次数: 0

摘要

暴露于颗粒物 2.5(PM2.5)会对多个器官系统造成损害。鉴于衰老也会改变免疫系统的细胞性和反应以及下丘脑-垂体-肾上腺、性腺和甲状腺轴的功能障碍,研究长期暴露于PM2.5是否会在这些方面与衰老发生相互作用势在必行。在这项研究中,两个月大的Sprague-Dawley大鼠暴露于真实世界的PM2.5中长达16个月。接触 PM2.5 会减少雄性大鼠外周血中 CD4+ T 细胞和 CD8+ T 细胞的相对数量,增加 B 细胞的相对数量。相反,在雌性大鼠的血液中只看到 CD4+ T 细胞相对数量的减少。这些变化导致雌雄大鼠循环系统中的促炎因子白细胞介素-6 和肿瘤坏死因子-α 水平升高,其中雌性大鼠的白细胞介素-1β 水平也有所升高。此外,只有在女性受试者的海马体中才能看到白细胞介素-6的升高,而肿瘤坏死因子-α浓度的升高在女性脑区很普遍,但仅限于男性的下丘脑。暴露于PM2.5后,男女受试者体内的荷尔蒙都明显减少。其中包括由下丘脑-垂体-肾上腺轴产生的促肾上腺皮质激素释放激素和皮质醇,以及由下丘脑-垂体-甲状腺轴产生的甲状腺释放激素和三碘甲状腺原氨酸等生物大分子的减少。由下丘脑-垂体-性腺轴产生的促性腺激素释放激素、黄体生成素和卵泡刺激素等激素成分也减少了。雄性大鼠的促肾上腺皮质激素水平下降,而雌性大鼠的促甲状腺激素水平下降。此外,睾酮、雌二醇和孕酮等性别特异性荷尔蒙也出现下降。这些发现极大地丰富了我们对与PM2.5相互作用相关的潜在长期健康影响的理解,尤其是在老龄人口中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intersection of Aging and Particulate Matter 2.5 Exposure in Real World: Effects on Inflammation and Endocrine Axis Activities in Rats.

Exposure to particulate matter 2.5 (PM2.5) is detrimental to multiple organ systems. Given the factor that aging also alters the cellularity and response of immune system and dysfunction of hypothalamic-pituitary-adrenal, -gonad and -thyroid axes, it is imperative to investigate whether chronic exposure to PM2.5 interacts with aging in these aspects. In this study, two-months-old Sprague-Dawley rats were exposed to real world PM2.5 for 16 months. PM2.5 exposure diminished the relative numbers of CD4+ T cells and CD8+ T cells and increased the relative number of B cells in the peripheral blood of male rats. Conversely, only reduced relative number of CD4+ T cells was seen in the blood of female rats. These shifts resulted in elevated levels of proinflammatory factors interleukin-6 and tumor necrosis factor-α in the circulatory systems of both sex, with females also evidencing a rise in interleukin-1β levels. Moreover, heightened interleukin-6 was solely discernible in the hippocampus of female subjects, while increased tumor necrosis factor-α concentrations were widespread in female brain regions but confined to the male hypothalamus. Notable hormonal decreases were observed following PM2.5 exposure in both sex. These comprised declines in biomolecules such as corticotrophin-releasing hormone and cortisol, generated by the hypothalamic-pituitary-adrenal axis, and thyroid-releasing hormone and triiodothyronine, produced by the hypothalamic-pituitary-thyroid axis. Hormonal elements such as gonadotropin-releasing hormone, luteinizing hormone, and follicle-stimulating hormone, derived from the hypothalamic-pituitary-gonad axis, were also diminished. Exclusive to male rats was a reduction in adrenocorticotropic hormone levels, whereas a fall in thyroid-stimulating hormone was unique to female rats. Decreases in sex-specific hormones, including testosterone, estradiol, and progesterone, were also noted. These findings significantly enrich our comprehension of the potential long-term health repercussions associated with PM2.5 interaction particularly among the aging populace.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
International Journal of Endocrinology
International Journal of Endocrinology ENDOCRINOLOGY & METABOLISM-
CiteScore
5.20
自引率
0.00%
发文量
147
审稿时长
1 months
期刊介绍: International Journal of Endocrinology is a peer-reviewed, Open Access journal that provides a forum for scientists and clinicians working in basic and translational research. The journal publishes original research articles, review articles, and clinical studies that provide insights into the endocrine system and its associated diseases at a genomic, molecular, biochemical and cellular level.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信