天津医药 ›› 2018, Vol. 46 ›› Issue (3): 239-245.doi: 10.11958/20171286

• 实验研究 • 上一篇    下一篇

替米沙坦对高脂饲养OLETF大鼠心肌重构及PPARγ表达的影响

赵紫琴,郑喜兰,雒瑢,田凤石,方涛    

  1. 1天津市天津医院病理科(邮编300211);2天津市海河医院心血管内科;3天津市胸科医院内分泌科;4天津市第四中心医院心血管内科
  • 收稿日期:2017-11-17 修回日期:2018-01-26 出版日期:2018-03-15 发布日期:2018-03-23
  • 通讯作者: 赵紫琴 E-mail:starelr_99@126.com
  • 基金资助:
    天津市应用基础与前沿技术研究计划青年项目资助(15JCQNJC13100)

The effect of telmisartan on myocardial remodeling and expression of PPARγ in myocardial tissue in high-fat fed OLETF rats

ZHAO Zi-qin,ZHENG Xi-lan,LUO Rong, TIAN feng-shi, FANG Tao   

  1. 1 Department of Pathology, Tianjin Hospital, Tianjin, 300211, China; 2 Department of Vasculocardiology, Tianjin Chest Hospital; 3 Department of Endocrinology, the Fourth Center Hospital of Tianjin;4 Department of Vasculocardiology, Tianjin Haihe Hospital
  • Received:2017-11-17 Revised:2018-01-26 Published:2018-03-15 Online:2018-03-23

摘要: 目的 探讨替米沙坦对高脂饲养的 OLETF 大鼠心肌重构及过氧化物酶体增殖物激活受体 γ(PPARγ)表达的影响。方法 4 周龄雄性 OLETF 大鼠 28 只,高脂喂养。22 周龄时称质量后随机分为替米沙坦组[O-T 组,5mg/ (kg·d),n=10],吡格列酮组[O-P 组,10 mg/ (kg·d),n=8]及无干预对照组[O-C 组,等体积生理盐水,n=10],连续给药 26 周;选取性别、周龄匹配的正常非糖尿病 LETO 大鼠为空白对照(LETO 组,n=12)。分别于 22 周龄和 48 周龄时行口服葡萄糖耐量试验(OGTT)检测大鼠 2 型糖尿病(T2DM)和糖耐量异常(IGT)发病情况。48 周龄时给药结束后每组随机抽取 5 只大鼠行高胰岛素-正糖钳夹实验,计算 60~120 min 的葡萄糖输注速度(GIR60-120)。实验结束时处死动物,分离心脏,称量心脏质量(HW)和体质量(BW),以 HW/BW 判定心肌肥厚情况。ELISA 法测定血清PPARγ、肿瘤坏死因子(TNF)-α、白细胞介素(IL)-6 水平,放射免疫法测定血清脂联素水平。Real-time PCR 检测心肌组织中 PPARγ1、PPARγ2 及 IL-6 mRNA 表达水平,Western blot 法检测心肌组织中 PPARγ、脂联素、IL-6 及核因子(NF)-κB 蛋白表达水平。光镜和电镜下分别观察各组大鼠心肌常规病理改变(HE 染色、Masson 染色、PAS 染色)和超微结构改变。结果 22 周龄时,各组大鼠均未发生 T2DM 及 IGT。48 周龄时 O-C 组 7 只发展为 T2DM,2 只IGT;O-T 组 1 只 T2DM,3 只 IGT;其他 2 组未见 T2DM 和 IGT。48 周龄时,O-P 组、O-T 组 GIR60-120及 HW/BW 均明显低于 O-C 组(P<0.05),同时 O-T 组大鼠收缩压(SBP)、舒张压(DBP)较其他 3 组明显下降(P<0.05)。与 O-C 组相比,O-T 组血清 IL-6、TNF-α 水平下降,脂联素和 PPARγ 水平则明显升高(P<0.05);O-P 及 O-T 组间上述指标差异均无统计学意义。Real-time PCR 及 Westen blot 结果显示,与 O-C 组相比,O-T 组 PPARγ1 mRNA 表达升高、IL-6 表达降低,O-P 组及 O-T 组 PPARγ、脂联素的蛋白表达均明显升高,而 NF-κB 及 IL-6 蛋白表达下降(均 P<0.05)。光镜和电镜下可见 O-C 组心肌细胞受损严重,纤维排列紊乱,胞浆溶解,心肌间质中出现大量胶原纤维增生,糖原和脂褐素沉积,肌原纤维断裂和核周扩张,心肌线粒体明显受损甚至溶解,O-P 组和 O-T 组心肌纤维排列整齐,无明显糖原沉积,心肌超微结构损害明显减轻。结论 小剂量替米沙坦可上调高脂饲养 OLETF 大鼠循环及心肌组织中 PPARγ 的表达,减轻心肌纤维化,延缓心肌重构。

关键词: 大鼠, 近交 OLETF, 心室重构, 糖尿病, 2 型, 过氧化物酶体增殖物激活受体 γ, 替米沙坦

Abstract: Abstract: Objective To investigate the effect of telmisartan on the expression of peroxisome proliferator activated receptor gamma (PPARγ) and its regulation in myocardial remodeling in spontaneously type 2 diabetic male Otsuka Long-Evans Tokushima Fatty (OLETF) rats fed with high-fat diet. Methods Twenty-eight four-week-old male OLETF rats were fed with high-fat diet. From 22-week of age, the pre-diabetic OLETF rats were randomly assigned to three groups:telmisartan-treated group [O-T group, 5 mg/(kg·d), n=10], pioglitazone-treated group [O-P group, 10 mg/(kg·d), n=8] and untreated group ( O-C group, equal volume of normal saline, n=10),continuously administration for 22-week. Twelve sex and age matched Long-Evans Tokushima Otsuka (LETO) rats were used as control (LETO group). At 22 and 48-week of age,the glucose tolerance of the rats was assessed by the oral glucose tolerance test (OGTT). At 48 weeks of age, five rats were randomly selected from each group, and clamp experiments were carried out. The glucose infusion rate from 60 min to 120min (GIR60-120) was measured. All rats were sacrificed and the myocardial tissues were dissected. The ratio of heart weight to body weight (HW/BW) was calculated. Blood samples were collected, and serum PPARγ, tumor necrosis factor-alpha(TNF-α), interleukin-6 (IL-6) and adiponectin were measured using ELISA and radioimmunoassay. The mRNA expressions of IL-6, PPARγ1 and PPARγ2 were measured by real-time PCR. The protein expression levels of PPARγ, adiponectin, IL-6 and NF-κB were determined by Western blot assay. The myocardial pathological changes were observed under light microscope(HE staining, Masson staining and PAS staining), and ultrastructural changes were observed under transmission electron microscope. Results At 22-week of age, neither type 2 diabetes mellitus (T2DM) nor IGT were found in three groups. At 48-week of age, T2DM was found in seven rats of O-C group, and IGT was found in two rats. T2DM was found in one rat of O-C group, and IGT was found in three rats. Neither T2DM nor IGT was found in the other two groups. GIR60-120 and HW/BW were all significantly lower in the O-P group and O-T group than those of the O-C group at 48-week of age (P<0.05).Systolic blood pressure (SBP) and diastolic blood pressure (DBP) were significantly lower in O-T group than those in other three groups (P<0.05). Compared with the O-C group, the serum levels of PPARγ and adiponectin were significantly upregulated, whereas the serum levels of IL-6 and TNF-α were down-regulated by telmisartan administration in O-T group(P<0.05). There were no significant differences in the above indexes between O-P and O-T groups. The results of real-time PCR and Westen blot assay showed that the mRNA expression of PPARγ1 was increased, and IL-6 expression decreased in O-T group compared with those of O-C group. The protein expressions of PPARγ and adiponectin were increased, and protein expressions of NF-κB and IL-6 were significantly decreased in O-P group and O-T group compared with those of OC group (P<0.05). In the O-C group, the arrangernent of myocardial cells was irregular, myocardial fibers were swollen, a large amount of fibrotic tissue in the myocardial interstitium, and glycogen accumulation under light and electron microscope. Besides, myofibril breakage and perinuclear space expansion, myocardial mitochondria were apparently damaged or even dissolved. Compared with the O-C group, myocardial fibers arranged neatly, no obvious glycogen deposition and the ultrastructural changes of myocardium were obviously reduced in O-T group and O-P group.Conclusion Telmisartan can increase the expression level of PPARγ in the serum and myocardial tissue, reduce myocardial fibrosis and alleviate cardiac remodeling in the high-fat-diet OLETF rats.

Key words: rats, inbred OLETF, ventricular remodeling, diabetes mellitus, type 2, PPARγ, telmisartan

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