Literature DB >> 16983932

The newly developed calcium antagonist, azelnidipine, increases drain volume in continuous ambulatory peritoneal dialysis patients.

Hiromichi Suzuki1, Tsutomu Inoue, Kazuhiro Kobayashi, Junko Shoda, Hidetomo Nakamoto.   

Abstract

Many patients undergoing continuous ambulatory peritoneal dialysis (CAPD) receive antihypertensive agents, including calcium antagonists, which produce reflex tachycardia through activation of the sympathetic nervous system. Azelnidipine, a newly developed calcium antagonist, has unique characteristics in that it causes less reflex stimulation of the sympathetic nervous system. In the present study, we used a crossover method to compare the effects of amlodipine (5-10 mg daily) and azelnidipine (8-16 mg daily) on drain volume and weekly creatinine clearance in 9 CAPD patients (3 women, 6 men; mean age: 64 +/- 5 years; mean duration of CAPD: 1.8 +/- 0.6 years). Each calcium antagonist was administered for 3 months and then switched for the other. As compared with amlodipine, azelnidipine increased drain volume by 13% +/- 2% (p < 0.05) and weekly creatinine clearance by 12% +/- 2% (p < 0.05). At the same time, we observed no significant differences in blood pressure and urine volume. The increases in drain volume produced by azelnidipine resulted from less activation of the sympathetic nervous system. We therefore suggest that activation of the sympathetic nervous system induced by calcium antagonists may be important in the regulation of drain volume in CAPD patients.

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Year:  2006        PMID: 16983932

Source DB:  PubMed          Journal:  Adv Perit Dial        ISSN: 1197-8554


  2 in total

1.  Aliskiren-induced chyloperitoneum in a patient on peritoneal dialysis.

Authors:  Y Saka; H Tachi; H Sakurai; M Tawada; A Sawai; Y Shimamura; M Mizuno; S Maruyama; S Matsuo; Y Ito
Journal:  Perit Dial Int       Date:  2012 Jan-Feb       Impact factor: 1.756

2.  Tolvaptan increases urine and ultrafiltration volume for patients with oliguria undergoing peritoneal dialysis.

Authors:  Tohru Iwahori; Masatoshi Esaki; Hayao Hinoue; Shinga Esaki; Yukumi Esaki
Journal:  Clin Exp Nephrol       Date:  2013-10-11       Impact factor: 2.801

  2 in total

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