Literature DB >> 20337636

Beneficial effects of L- and N-type calcium channel blocker on glucose and lipid metabolism and renal function in patients with hypertension and type II diabetes mellitus.

Takashi Masuda1, Misao N Ogura, Tatsumi Moriya, Naonobu Takahira, Takuya Matsumoto, Toshiki Kutsuna, Miyako Hara, Naoko Aiba, Chiharu Noda, Tohru Izumi.   

Abstract

It has been proved that cilnidipine has N-type calcium channels inhibitory activity as well as L-type calcium channels and inhibits excessive release of norepinephrine from the sympathetic nerve ending. This study was undertaken to compare the efficacy of amlodipine (an inhibitor of L-type calcium channels) and cilnidipine (an inhibitor of both L-type and N-type calcium channels) in patients with hypertension and type II diabetes mellitus. Seventy-seven hypertensive patients were divided into two groups according to presence/absence of type II diabetes mellitus. In these two groups of patients, the effects of amlodipine and cilnidipine on glucose and lipid metabolism and renal function were compared. As for glucose and lipid metabolism, homeostasis model assessment insulin resistance (HOMA-R) level in the non-diabetic group and triglyceride in the diabetes group were significantly lower with cilnidipine than with amlodipine. As regards renal function in the diabetic group, estimated glomerular filtration rate (eGFR) was significantly higher and urinary albumin/creatinine ratio was significantly lower with cilnidipine than with amlodipine. Cilnidipine which inhibits N-type calcium channels is more useful for patients with hypertension and diabetes mellitus from its effects on glucose and lipid metabolism and renal function.
© 2010 Blackwell Publishing Ltd.

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Year:  2011        PMID: 20337636     DOI: 10.1111/j.1755-5922.2009.00126.x

Source DB:  PubMed          Journal:  Cardiovasc Ther        ISSN: 1755-5914            Impact factor:   3.023


  8 in total

Review 1.  The fourth-generation Calcium channel blocker: cilnidipine.

Authors:  K Sarat Chandra; G Ramesh
Journal:  Indian Heart J       Date:  2013-12

2.  N-type calcium channel inhibition with cilnidipine elicits glomerular podocyte protection independent of sympathetic nerve inhibition.

Authors:  Bai Lei; Daisuke Nakano; Yoshihide Fujisawa; Ya Liu; Hirofumi Hitomi; Hiroyuki Kobori; Hirohito Mori; Tsutomu Masaki; Katsuhiko Asanuma; Yasuhiko Tomino; Akira Nishiyama
Journal:  J Pharmacol Sci       Date:  2012-07-21       Impact factor: 3.337

Review 3.  Ion channels and transporters in diabetic kidney disease.

Authors:  Denisha Spires; Anna D Manis; Alexander Staruschenko
Journal:  Curr Top Membr       Date:  2019-02-18       Impact factor: 3.049

4.  Serum Triglyceride Lowering Effect of Cilnidipine in Patients With Essential Hypertension.

Authors:  Prakash Kumar; Arijit Das; Satish Chandra; Manju Gari; U S P Keshri; Kusum Kumari
Journal:  Cardiol Res       Date:  2016-11-03

5.  Genomics of lipid-laden human hepatocyte cultures enables drug target screening for the treatment of non-alcoholic fatty liver disease.

Authors:  Stephanie Breher-Esch; Nishika Sahini; Anna Trincone; Christin Wallstab; Jürgen Borlak
Journal:  BMC Med Genomics       Date:  2018-12-14       Impact factor: 3.063

6.  Modifiable Variables Are Major Risk Factors for Posttransplant Diabetes Mellitus in a Time-Dependent Manner in Kidney Transplant: An Observational Cohort Study.

Authors:  Débora Dias de Lucena; João Roberto de Sá; José O Medina-Pestana; Érika Bevilaqua Rangel
Journal:  J Diabetes Res       Date:  2020-03-18       Impact factor: 4.011

7.  Cilnidipine and magnesium sulfate supplement ameliorates hyperglycemia, dyslipidemia and inhibits oxidative-stress in fructose-induced diabetic rats.

Authors:  Most Sumaiya Khatun Kali; Md Rafiqul Islam Khan; Ranjan Kumar Barman; Md Farhad Hossain; Mir Imam Ibne Wahed
Journal:  Heliyon       Date:  2021-12-26

8.  Comparison of the antialbuminuric effects of L-/N-type and L-type calcium channel blockers in hypertensive patients with diabetes and microalbuminuria: the study of assessment for kidney function by urinary microalbumin in randomized (SAKURA) trial.

Authors:  Katsuayuki Ando; Kenji Ueshima; Sachiko Tanaka; Shinji Kosugi; Tosiya Sato; Hiroaki Matsuoka; Kazuwa Nakao; Toshiro Fujita
Journal:  Int J Med Sci       Date:  2013-07-30       Impact factor: 3.738

  8 in total

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