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Combination therapy with renin-angiotensin-aldosterone system inhibitor telmisartan and serine protease inhibitor camostat mesilate provides further renoprotection in a rat chronic kidney disease model
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نویسنده
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narita y. ,ueda m. ,uchimura k. ,kakizoe y. ,miyasato y. ,mizumoto t. ,morinaga j. ,hayata m. ,nakagawa t. ,adachi m. ,miyoshi t. ,sakai y. ,kadowaki d. ,hirata s. ,mukoyama m. ,kitamura k.
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منبع
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journal of pharmacological sciences - 2016 - دوره : 130 - شماره : 2 - صفحه:110 -116
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چکیده
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We previously reported that camostat mesilate (cm) had renoprotective and antihypertensive effects in rat ckd models. in this study,we examined if cm has a distinct renoprotective effect from telmisartan (te),a renin-angiotensin-aldosterone system (ras) inhibitor,on the progression of ckd. we evaluated the effect of cm (400 mg/kg/day) and/or te (10 mg/kg/day) on renal function,oxidative stress,renal fibrosis,and ras components in the adenine-induced rat ckd model following 5-weeks treatment period. the combination therapy with cm and te significantly decreased the adenine-induced increase in serum creatinine levels compared with each monotherapy,although all treatment groups showed similar reduction in blood pressure. similarly,adenine-induced elevation in oxidative stress markers and renal fibrosis markers were significantly reduced by the combination therapy relative to each monotherapy. furthermore,the effect of the combination therapy on plasma renin activity (pra) and plasma aldosterone concentration (pac) was similar to that of te monotherapy,and cm had no effect on both pra and pac,suggesting that cm has a distinct pharmacological property from ras inhibition. our findings indicate that cm could be a candidate drug for an add-on therapy for ckd patients who had been treated with ras inhibitors. © 2016 japanese pharmacological society. production and hosting by elsevier b.v.
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کلیدواژه
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Camostat mesilate; Chronic kidney diseases; Combination therapy; Serine protease inhibitor; Telmisartan
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آدرس
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center for clinical pharmaceutical sciences,kumamoto university,5-1 oe-honmachi,chuo-ku,kumamoto 862-0973, Japan, department of nephrology,kumamoto university graduate school of medical sciences,1-1-1 honjo,chuo-ku,kumamoto 860-8556, Japan, department of internal medicine iii,faculty of medicine,university of yamanashi,1110 shimokato,chuo-shi,yamanashi 409-3898, Japan, department of nephrology,kumamoto university graduate school of medical sciences,1-1-1 honjo,chuo-ku,kumamoto 860-8556, Japan, department of nephrology,kumamoto university graduate school of medical sciences,1-1-1 honjo,chuo-ku,kumamoto 860-8556, Japan, department of nephrology,kumamoto university graduate school of medical sciences,1-1-1 honjo,chuo-ku,kumamoto 860-8556, Japan, department of nephrology,kumamoto university graduate school of medical sciences,1-1-1 honjo,chuo-ku,kumamoto 860-8556, Japan, department of nephrology,kumamoto university graduate school of medical sciences,1-1-1 honjo,chuo-ku,kumamoto 860-8556, Japan, department of nephrology,kumamoto university graduate school of medical sciences,1-1-1 honjo,chuo-ku,kumamoto 860-8556, Japan, department of nephrology,kumamoto university graduate school of medical sciences,1-1-1 honjo,chuo-ku,kumamoto 860-8556, Japan, department of nephrology,kumamoto university graduate school of medical sciences,1-1-1 honjo,chuo-ku,kumamoto 860-8556, Japan, research headquarters,ono pharmaceutical co.,ltd.,1-8-2 kyutaromachi,chuo-ku,osaka 541-8564, Japan, center for clinical pharmaceutical sciences,kumamoto university,5-1 oe-honmachi,chuo-ku,kumamoto 862-0973, Japan, center for clinical pharmaceutical sciences,kumamoto university,5-1 oe-honmachi,chuo-ku,kumamoto 862-0973, Japan, department of nephrology,kumamoto university graduate school of medical sciences,1-1-1 honjo,chuo-ku,kumamoto 860-8556, Japan, department of internal medicine iii,faculty of medicine,university of yamanashi,1110 shimokato,chuo-shi,yamanashi 409-3898, Japan
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Authors
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