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性别差异在急性肾损伤向慢性肾脏病进展中的作用

Gender Differences in the Acute Kidney Injury to Chronic Kidney Disease Transition.

机构信息

Molecular Physiology Unit, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, Mexico City, Mexico.

Departament of Nephrology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico.

出版信息

Sci Rep. 2017 Sep 25;7(1):12270. doi: 10.1038/s41598-017-09630-2.

DOI:10.1038/s41598-017-09630-2
PMID:28947737
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5612964/
Abstract

This study evaluated if there is a sexual dimorphism in the acute kidney injury (AKI) to chronic kidney disease (CKD) transition and the time-course of the potential mechanisms involved in the dimorphic response. Female and male rats were divided into sham-operated or underwent 45-min renal ischemia (F + IR, and M + IR). All groups were studied at 24-h and 1, 2, 3, or 4-months post-ischemia. Additionally, oophorectomized rats were divided into sham or IR groups. After 24-h, AKI extent was simllar in females and males, but female rats exhibited less oxidative stress and increased renal GSH content. After 4-months and despite similar AKI, the M + IR group developed CKD characterized by proteinuria, tubulointerstitial fibrosis, glomerular hypertrophy, increased oxidative stress and a reduction in HIF1α and VEGF from the 1-month and persisting throughout the time-course studied. Interestingly, the F + IR group did not develop CKD due to lesser oxidative stress and increased eNOS, TGFβ and HIF1α mRNA levels from the 1-month after IR. Whereas, oophorectomized rats did develop CKD. We found a sexual dimorphic response in the AKI to CKD transition. Early antioxidant defense and higher TGFβ, HIF1α and eNOS were among the renoprotective mechanisms that the F + IR group demonstrated.

摘要

这项研究评估了急性肾损伤 (AKI) 向慢性肾脏病 (CKD) 转变过程中是否存在性别二态性,以及涉及这种二态性反应的潜在机制的时程。雌性和雄性大鼠分为假手术或接受 45 分钟肾缺血 (F+IR 和 M+IR)。所有组均在缺血后 24 小时和 1、2、3 或 4 个月进行研究。此外,卵巢切除大鼠分为假手术或 IR 组。在 24 小时后,雌性和雄性大鼠的 AKI 程度相似,但雌性大鼠的氧化应激较小,肾 GSH 含量增加。4 个月后,尽管 AKI 相似,但 M+IR 组发展为 CKD,表现为蛋白尿、肾小管间质纤维化、肾小球肥大、氧化应激增加以及 HIF1α 和 VEGF 从 1 个月开始减少,并持续整个研究过程。有趣的是,F+IR 组由于氧化应激较小和 TGFβ、HIF1α 和 eNOS mRNA 水平从 IR 后 1 个月开始升高,因此未发展为 CKD。而卵巢切除大鼠确实发展为 CKD。我们发现 AKI 向 CKD 转变存在性别二态性。早期抗氧化防御和更高的 TGFβ、HIF1α 和 eNOS 是 F+IR 组表现出的肾保护机制之一。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a91/5612964/3d2067be2ffe/41598_2017_9630_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a91/5612964/a78d35eca257/41598_2017_9630_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a91/5612964/e868cc22a231/41598_2017_9630_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a91/5612964/6612a2b34a3b/41598_2017_9630_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a91/5612964/789b706d305c/41598_2017_9630_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a91/5612964/8059ad266adf/41598_2017_9630_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a91/5612964/1e3613a994c5/41598_2017_9630_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a91/5612964/3d2067be2ffe/41598_2017_9630_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a91/5612964/a78d35eca257/41598_2017_9630_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a91/5612964/e868cc22a231/41598_2017_9630_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a91/5612964/6612a2b34a3b/41598_2017_9630_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a91/5612964/789b706d305c/41598_2017_9630_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a91/5612964/8059ad266adf/41598_2017_9630_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a91/5612964/1e3613a994c5/41598_2017_9630_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a91/5612964/3d2067be2ffe/41598_2017_9630_Fig7_HTML.jpg

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