摘要
目的 观察结缔组织生长因子 (CTGF)mRNA在 5 / 6肾切除大鼠肾皮质的表达特点和羟甲基戊二酰辅酶A(HMG CoA)还原酶抑制剂氟伐他汀的调节作用。方法 将 2 4只 5 / 6肾切除大鼠随机分为未治疗的 5 / 6肾切除组 (模型组 ,12只 )和氟伐他汀治疗的 5 / 6肾切除组 (治疗组 ,12只 ) ,另设6只假手术大鼠作为对照。氟伐他汀治疗 (7mg·kg-1·d-1) 13周后 ,检测尿蛋白排泄、血清尿素氮和肌酐含量 ,用RT PCR法检测肾皮质CTGFmRNA表达 ,免疫组织化学检测肾小球转化生长因子 β1(TGF β1)、IV型胶原和纤连蛋白的表达水平 ,并评价肾脏病变和肾小球硬化指数 (GSI)。 结果 实验终止时 ,模型组尿蛋白排泄 (30 5 4mg/ 2 4h)显著高于假手术组 (5 6mg/ 2 4h ,P <0 0 1) ,氟伐他汀治疗的大鼠尿蛋白排泄 (2 30 9mg/ 2 4h)明显低于模型组 (P <0 0 5 )。与假手术组相比 ,模型组血清尿素氮(P <0 0 1)和肌酐 (P <0 0 5 )水平均明显增高 ,氟伐他汀治疗使血清尿素氮和肌酐的含量明显降低。模型组GSI为 4 1 8± 11 5 ,明显高于假手术组 (2 2± 1 3,P <0 0 1) ,治疗组GSI(2 3 4± 6 1)明显低于模型组 (P <0 0 5 )。肾皮质CTGFmRNA表达水平约为假手术组的 3倍 (P <0 0 1) ,而在治疗组其表达水平减少 5 5 4 %。
Objective To investigate the connective tissue growth factor (CTGF) mRNA expression in the renal cortex of 5/6 nephrectomized rats and its modulation by fluvastatin, a 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitor. Methods Twenty-four rats underwent operation 2 times: during the first operation 2/3 of the left kidney was resected, and the right kidney was resected completely one week after. The 24 5/6 nephrectomized rats were randomly divided into 2 groups: untreated 5/6 nephrectomized group (model group, n=12) and fluvastatin-treated 5/6 nephrectomized group (treatment group, fluvastatin was orally administered 7 mg·kg -1 ·d -1 for 13 weeks, n=12),and 6 sham-operated rats served as control (sham operation group). In the weeks 2, 4, 8, and 13 after the second operation metabolic cage was used to collect the 24-hour urine 2 times. Urine protein was examined by biuret reaction so as to calculate urinary protein excretion. By the end of experiment blood was collected to examine the serum cholesterol, triglyceride, urea nitrogen, and creatinine contents. The rats were killed and their kidneys taken out. The CTGF mRNA expression in the renal cortex was detected by RT-PCR. Immunohistochemstry was used to examine the expression of transforming growth factor-β1(TGF-β1), type IV collagen and fibronectin in the glomeruli. Renal pathological changes and glomerular sclerosis index (GSI) were evaluated as well. Results At the end of the experiment, the mean urinary protein excretion in the model group was 305.4 mg/24 h, significantly higher than that in the treatment group (230.9 mg/24 h, P <0.01) and the sham operation group (5.6 mg/ 24 h, P <0.01) The serum urea nitrogen of the model group was (24.5±4.9 )mmol/L , significantly higher than that of the treatment group[ (15.8±3.9) mmol/L, P <0.05] and that of the sham-operated group (7.4±0.3 mmol/L. P <0.01). The serum creatinine ( P <0.05) of the model group was 88 μmol/L±14 μmol/L , significantly higher than that of the treatment group [(58±5) μmol/L, P <0.05)] and that of the sham-operated group[(54±5) μmol/L. P <0.05]. The creatinine clearance rate of the model group was (1.7±0.7) ml·min -1 ·kg -1 , significantly lower than that of the treated group [(3.2±1.1) ml·min -1 ·kg -1 , P <0.05] and that of the sham-operated group[(3.9±1.5) ml·min -1 ·kg -1 , P <0.05]. The glomerular sclerosis index (GSI) in the model group was 41.8±11.5, significantly higher than that in the sham operation group (2.2±1.3, P <0.01) and the treatment group (23.4±6.1, P <0.05). The mean optical density of CTGF mRNA expression in the renal cortex of the model group was a 3 times that of the sham operation group, and the mean optical density of CTGF mRNA expression in the renal cortex of the treatment group was lower by 55.4% compared with that of the model group ( P <0.01). The glomerular expressions of TGF-β1, type IV collagen and fibronectin were significantly up-regulated in the model group in comparison with those in the sham operation group (all P <0.01). The glomerular proten expressions of TGF-β1, type IV collagen and fibronectin were significantly weaker in the fluvastatin treatment group as compared with the model group (all P <0.01).Conclusion CTGF mRNA expression is markedly upregulated in the renal cortex of 5/6 nephrectomized rats. Fluvastatin suppresses the increased CTGF mRNA expression in renal cortex and ameliorates the glomerular extracellular matrix accumulation.
出处
《中华医学杂志》
CAS
CSCD
北大核心
2003年第16期1428-1432,共5页
National Medical Journal of China
基金
国家自然科学基金资助项目 (3 9870 3 12 )
