首页> 外文期刊>Journal of Molecular Neuroscience: MN >Protective Effect of PACAP on Ischemia/Reperfusion-Induced Kidney Injury of Male and Female Rats: Gender Differences
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Protective Effect of PACAP on Ischemia/Reperfusion-Induced Kidney Injury of Male and Female Rats: Gender Differences

机译:PACAP对男性和女性大鼠缺血/再灌注肾损伤的保护作用:性别差异

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摘要

Pituitary adenylate cyclase-activating polypeptide (PACAP) is a neuropeptide that exerts general cytoprotective effects, including protection in different kidney disorders. The aim of our study was to investigate the ischemia/reperfusion-induced kidney injury of male and female rats to confirm the protective effects of PACAP in the kidney and to reveal possible gender differences.Male and female Wistar rats underwent unilateral renal artery clamping followed by 24-h, 48-h, or 14-day reperfusion. PACAP was administered intravenously before arterial clamping in half of the rats. Tubular damage, cytokine expression pattern, oxidative stress marker, antioxidative statusand signaling pathways were evaluated using histology, immunohistology, cytokine array, PCR, and Western blot. Tubular damage was significantly less severe in the PACAP-treated male and female rats compared to controls. Results of female animals were significantly better in both treated and untreated groups. Cytokine expression, oxidative stress marker and antioxidative statusconfirmed the histological results. We also revealed that PACAP counteracted the decreased PKA phosphorylation, influenced the expression of BMP2 and BMP4, and increased the expression of the protein Smad1.We conclude that PACAP is protective in ischemia/reperfusion-induced kidney injury in both sexes, but females had markedly less pronounced injury after ischemia/reperfusion, possibly also involving further protective factors, the investigation of which could have future therapeutic value in treating ischemic kidney injuries.
机译:垂体腺苷酸环酶活化多肽(PACAP)是一种神经肽,其施加一般的细胞保护作用,包括在不同的肾病中的保护。我们的研究目的是探讨雌性和雌性大鼠的缺血/再灌注诱导的肾损伤,以确认PACAP在肾脏中的保护作用,并揭示可能的性别差异。患者和女性Wistar大鼠接受单侧肾动脉夹紧术后。 24-H,48小时或14天再灌注。 PACAP在大鼠一半的动脉夹紧前静脉内施用。使用组织学,免疫组织学,细胞因子阵列,PCR和Western印迹评估管状损伤,细胞因子表达模式,氧化应激标记,抗氧化状态和信号通路。与对照相比,PACAP处理的雄性大鼠的管状损伤显着不太严重。在治疗和未经处理的群体中,雌性动物的结果显着更好。细胞因子表达,氧化应激标记物和抗氧化性质确认了组织学结果。我们还透露了PACAP抵消了PKA磷酸化降低,影响了BMP2和BMP4的表达,并增加了蛋白质Smad1的表达。我们得出的结论是PACAP在两性中的缺血/再灌注诱导的肾脏损伤中受到保护,但女性显着缺血/再灌注后的损伤不那么明显,可能还涉及进一步的保护因素,对其治疗缺血性肾脏损伤的未来治疗价值可能具有进一步的保护因素。

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