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