首页|A-485 通过抑制 P300/CBP 诱导的 H3K18ac/H3K27ac减轻糖尿病肾小管细胞脂质沉积

A-485 通过抑制 P300/CBP 诱导的 H3K18ac/H3K27ac减轻糖尿病肾小管细胞脂质沉积

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目的 观察A-485对糖尿病小鼠肾小管损伤的保护作用及机制.方法 将18只雄性C57BL/6J小鼠随机分为对照组、糖尿病肾病(diabetic kidney disease,DKD)组和A-485治疗组.DKD小鼠模型构建采用高脂饲料饲喂8周联合腹腔注射链脲佐菌素5天的方法.随后,A-485治疗组隔日给予1次A-485(10 mg/kg)腹腔注射,共4周.治疗结束后,检测小鼠肾功能、P300 酶活性及脂质沉积情况;Western blot 法检测 SREBP-1、FASN、ACC、ChREBP、P300、CBP、H3K18ac 和 H3K27ac 蛋白的表达水平.结果 与对照小鼠相比,DKD小鼠FBG(2.52倍)、BUN(2.89倍)、Scr(2.13倍)及UAE(4.21倍)显著升高(P<0.01);A-485干预能够降低BUN(0.511倍)、Scr(0.636倍)及UAE(0.574倍)的水平(P<0.01).电镜及油红O染色结果显示,A-485干预抑制糖尿病小鼠肾小管细胞内脂滴形成及SREBP-1(0.544倍)、FASN(0.449倍)、ACC(0.306倍)、ChREBP(0.317倍)蛋白高表达(P<0.01).同时,A-485干预下调P300酶活性(0.546倍),抑制H3K18ac(0.337倍)和H3K27ac(0.308倍)的表达(P<0.01).结论 A-485能够明显改善糖尿病小鼠肾组织脂代谢紊乱,该作用可能是通过抑制P300诱导的H3K18ac和H3K27ac实现的.
A-485 alleviates tubular lipid accumulation by inhibiting H3K18ac/H3K27ac induced by P300/CBP in diabetic mice
Purpose To investigate the protective effect and mechanism of A-485 on renal tubular injury in diabetic mice.Methods Eighteen male C57BL/6J mice were randomly divided into three groups:Control group,diabetic kidney dis-ease(DKD)group and A-485 treatment group.The DKD mice model was established by feeding high-fat diet for 8 weeks and intraperitoneal injection of streptozotocin for 5 days.Subsequent-ly,the A-485 treatment group was given A-485(10 mg/kg/day)by intraperitoneal injection every other day for 4 weeks.After treatment,the renal function,P300 enzyme activity and lipid deposition in renal tissue were measured.Western blot a-nalysis was performed to detect SREBP-1,FASN,ACC,ChREBP,P300,CBP,H3K18ac and H3K27ac protein levels.Results Compared with control mice,the levels of FBG,BUN,Scr and UAE were significantly increased in diabetic mice(FBG:2.52 times,BUN:2.89 times,Scr:2.13 times,UAE:4.21 times),while diabetic mice treatment with A-485 exhibi-ted a remarkable decrease on BUN,Scr and UAE(BUN:0.511 times,Scr:0.636 times,UAE:0.574 times,P<0.01).The results of the transmission electron microscopy and oil red O stai-ning showed that A-485 treatment prevents lipid droplets forma-tion and up-regulation of SREBP-1,FASN,ACC and ChREBP in renal tubular cells of diabetic mice(SREBP-1:0.544 times,FASN:0.449 times,ACC:0.306 times,ChREBP:0.317 times,P<0.01).Furthermore,A-485 intervention downregu-lated the enzyme activity of P300(0.546 times)and suppressed the expression of H3K18ac(0.337 times)and H3K27ac(0.308 times,P<0.01).Conclusion A-485 can significant-ly improve renal lipid metabolic disorder in diabetic mice,which may be achieved by inhibiting p300-induced H3K18ac and H3K27ac.

diabetic kidney diseaseP300/CBPA-485lipid accumulationacetylation

孟丽、朱艳、杨琰、吴婷、任韫卓、杜林珊、曾士洁、杜春阳

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河北医科大学电镜实验中心,石家庄 050017

河北医科大学病理学教研室,石家庄 050017

糖尿病肾病 P300/CBP A-485 脂质沉积 乙酰化

国家自然科学基金青年基金河北省高等学校科学技术研究项目青年基金河北省自然科学基金

82000773QN2021104H2022206463

2024

临床与实验病理学杂志
安徽医科大学,中华医学会安徽分会

临床与实验病理学杂志

CSTPCD北大核心
影响因子:0.776
ISSN:1001-7399
年,卷(期):2024.40(5)
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