脂联素抑制内质网应激干预慢性间歇性缺氧所致肾损伤
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(1. 江苏省老年医院呼吸内科,南京 210024;2. 南京医科大学第一附属人民医院呼吸内科,南京 210000)

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R322.3

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国家自然科学基金(81470273);临床医学科技专项——公共卫生关键技术应用(BL2014083)


Adiponectin protects rats against chronic intermittent hypoxia-induced kidney injury through inhibiting endoplasmic reticulum stress
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(1. Department of Respiratory Diseases, Jiangsu Province Geriatric Hospital, Nanjing 210024, China;2. Department of Respiratory Diseases, the First Affiliated Hospital of Nanjing Medical University, Nanjing 210000, China)

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    摘要:

    目的 探讨脂联素(Ad)对慢性间歇性缺氧(CIH)所致肾损伤的干预作用及相关机制。方法 60只成年Wistar大鼠随机分成4组:正常对照(NC)组、NC+Ad组、CIH组和CIH+Ad组。其中CIH组和CIH+Ad组大鼠接受CIH处理4个月。其余2组接受正常空气处理,同时NC+Ad组和CIH+Ad组大鼠接受Ad(10 μg)治疗,每周2次,持续4个月。荧光显微镜下观察活性氧(ROS)的水平。TUNEL染色检测肾脏细胞凋亡情况。Western blotting检测各组大鼠肾脏组织中GRP78、CHOP、IRE1、PERK、pro-ATF6蛋白的表达,以反映各组大鼠内质网应激情况。采用SPSS 17.0软件进行统计学分析。计量资料用均数±标准差([AKx-D]±s)表示,组间比较用t检验。结果 实验满4个月时,组间比较示各参数在NC与NC+Ad组间差异均无统计学意义(P均>0.05)。与NC组和NC+Ad组比较:(1)ROS水平在CIH组显著增高,而CIH+Ad组低于CIH组,但仍高于NC组和NC+Ad组(P均<0.05);(2)肾细胞凋亡率和反映凋亡的caspase-12和caspase-3蛋白水平在CIH组明显增加,CIH+Ad组较CIH组明显减少,但仍然高于NC组和NC+Ad组(P均<0.05);(3)CIH组肾脏组织的GRP78、CHOP、IRE1、PERK蛋白水平明显增加,在CIH+Ad组明显减少,但仍高于NC组和NC+Ad组(P均<0.05);pro-ATF6蛋白水平在CIH组明显降低,在CIH+Ad组有所增加,但仍然低于NC组和NC+Ad组(P均<0.05)。结论 CIH可以通过激活ROS和ERS相关的细胞凋亡途径导致肾脏损伤,而补充外源性Ad后,可能通过抑制ROS,进而抑制ERS,保护肾脏细胞。

    Abstract:

    Objective To determine the intervention effects of adiponectin (Ad) on rat kidney injury induced by chronic intermittent hypoxia (CIH), and investigate the underlying mechanisms. Methods Sixty adult Wistar rats were randomly divided into 4 groups:normal control (NC group), normal control plus Ad supplement (NC+Ad group), CIH, and CIH plus Ad supplement (CIH+Ad group) groups. The rats in both CIH and CIH+Ad groups were submitted to a CIH environment for 4 months, while the rats in NC and NC+Ad groups were housed with the normal air for 4 months. In addition, the rats in NC+Ad and CIH+Ad groups were treated with an intravenous injection of Ad at a dosage of 10 μg per injection, twice a week, for 4 successive months. Fluorescence microscopy was used to observe the levels of reactive oxygen species (ROS). TUNEL staining was employed to detect the apoptosis of renal cells. Western blotting was adopted to measure the expression levels of GRP78, CHOP, IRE1, PERK and pro-ATF6 in renal tissues of rats in each group to indicate the stress of endoplasmic reticulum in rats. SPSS statistics 17.0 was used to analyze the data. The measurement data were expressed as mean±standard deviation ([AKx-D]±s), and student’s t test was used for the comparison between the groups. Results In the end of 4 months’ treatment, no significant differences were found in all the parameters between the NC and NC+Ad groups (all P>0.05). Compared with the NC and NC+Ad groups, our findings were as follows:(1) ROS levels were significantly higher in the CIH group, while the levels in the CIH+Ad group was though lower than those in the CIH group, but higher than those in the NC and NC+Ad groups (all P<0.05); (2) the percentage of apoptotic renal cells and protein levels of caspase-12 and caspase-3 were all significantly higher in the CIH group, while in the CIH+Ad group, they were lower than in the CIH group, but still higher than in the NC and NC+Ad groups (all P<0.05); (3) the protein levels of GRP78, CHOP, IRE1 and PERK in the renal tissues were all significantly higher in the CIH group, while in CIH+Ad group, the levels were lower than in the CIH group, but higher than in the NC and NC+Ad groups (all P<0.05); the protein level of pro-ATF6 in the renal tissues was lower in the CIH group, while in the CIH+Ad group, the level was higher than in the CIH group, but lower than in the NC and NC+Ad groups (all P<0.05). Conclusion CIH induces kidney injury through activation of ROS and ERS-associated cellular apoptotic pathway, while exogenous Ad supplement protects the renal cells by inhibiting ROS and then ERS.

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高佳,朱选风,张希龙,陆甘,刘剑南.脂联素抑制内质网应激干预慢性间歇性缺氧所致肾损伤[J].中华老年多器官疾病杂志,2017,16(9):687~692

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  • 收稿日期:2017-06-16
  • 最后修改日期:2017-07-15
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  • 在线发布日期: 2017-09-26
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