Musio F, Carome M A, Bohen E M, Sabnis S, Yuan C M
Nephrology Service, Walter Reed Army Medical Center, Washington, DC 20307-5001, USA.
Ren Fail. 1997 Jan;19(1):33-46. doi: 10.3109/08860229709026258.
Glycine has been shown to protect against cisplatin (CP) nephrotoxicity in rats and to enhance the in vitro expression of heat-shock protein (hsp) 70 in renal epithelial cells following sublethal heat shock. We hypothesized that the protective effect of glycine against CP nephrotoxicity may be due to an up-regulation of Hsp 70 protein expression. Male Sprague-Dawley rats were divided into 4 treatment groups based upon infusion of glycine and injection of CP or their respective vehicles. At 5 days after treatment animals administered CP alone demonstrated a significant decrease in creatinine clearance compared to baseline (0.77 +/- 0.32 mL/min vs. 3.90 +/- 0.87 mL/min, p < 0.05). Treatment with glycine and CP attenuated this response, with no significant decline seen in creatinine clearance at day 5 compared to baseline (2.25 +/- 0.31 mL/min vs. 3.40 +/- 0.86 mL/min). Semiquantitative histological study revealed a marked decrease in proximal tubular injury at the juxtamedullary and outer medullary regions among animals treated with glycine and CP compared to those animals treated with CP alone. There were no differences in renal cortical and medullary Hsp 70 levels by Western immunoblotting between animals treated with glycine and CP compared to CP alone at 4 h and 5 days after treatment. Immunohistochemical studies of animals treated with CP alone revealed the diffuse presence of Hsp 70 in the cytoplasm of injured and necrotic proximal tubular cells 5 days after treatment. Animals receiving CP and glycine demonstrated a more focal presence of Hsp 70 restricted to injured proximal tubular cells, with no staining of uninjured cells. The protective effect of glycine in CP-induced acute and renal failure in the rat does not appear to be associated with enhancement of Hsp 70 expression.
甘氨酸已被证明可保护大鼠免受顺铂(CP)肾毒性影响,并能增强亚致死热休克后肾上皮细胞中热休克蛋白(hsp)70的体外表达。我们推测甘氨酸对CP肾毒性的保护作用可能归因于Hsp 70蛋白表达的上调。雄性Sprague-Dawley大鼠根据甘氨酸输注和CP注射或其各自的赋形剂分为4个治疗组。治疗后5天,单独给予CP的动物与基线相比肌酐清除率显著降低(0.77±0.32 mL/分钟对3.90±0.87 mL/分钟,p<0.05)。甘氨酸和CP联合治疗减弱了这种反应,与基线相比,第5天时肌酐清除率未见显著下降(2.25±0.31 mL/分钟对3.40±0.86 mL/分钟)。半定量组织学研究显示,与单独接受CP治疗的动物相比,接受甘氨酸和CP治疗的动物在近髓质和外髓质区域近端肾小管损伤明显减少。治疗后4小时和5天,通过蛋白质免疫印迹法检测,接受甘氨酸和CP治疗的动物与单独接受CP治疗的动物相比,肾皮质和髓质中Hsp 70水平无差异。单独接受CP治疗的动物的免疫组织化学研究显示,治疗后5天,损伤和坏死的近端肾小管细胞胞质中弥漫性存在Hsp 70。接受CP和甘氨酸治疗的动物显示Hsp 70更局限于损伤的近端肾小管细胞,未损伤细胞无染色。甘氨酸对大鼠CP诱导的急性肾衰竭的保护作用似乎与Hsp 70表达增强无关。