Literature DB >> 26057694

Pre-treatment with LCZ696, an orally active angiotensin receptor neprilysin inhibitor, prevents ischemic brain damage.

Hui-Yu Bai1, Masaki Mogi2, Hirotomo Nakaoka1, Harumi Kan-No1, Kana Tsukuda1, Toshiyuki Chisaka3, Xiao-Li Wang1, Masayoshi Kukida4, Bao-Shuai Shan1, Toshifumi Yamauchi3, Akinori Higaki4, Jun Iwanami1, Masatsugu Horiuchi1.   

Abstract

Angiotensin II receptor blockers (ARBs) are known to prevent ischemic brain damage after stroke. Natriuretic peptides, which are increased by a neprilysin inhibitor, are also reported to protect against brain damage. Therefore, we investigated the possible protective effect of valsartan (VAL) compared with LCZ696 (VAL+ neprilysin inhibitor; 1:1) after middle cerebral artery (MCA) occlusion. Eight-week-old male C57BL/6J mice were treated with VAL (3mg/kg per day) or LCZ696 (6mg/kg per day) for 2 weeks before MCA occlusion. Blood pressure and heart rate were measured by telemetry. Cerebral blood flow (CBF) was determined by laser-Doppler flowmetry. Ischemic area was evaluated by triphenytetrasodium chloride staining, and oxidative stress was determined by dihydroethidium staining. Blood pressure and heart rate were not significantly different before and after treatment. Pre-treatment with LCZ696 or VAL reduced the ischemic area, and this effect of LCZ696 was more marked than that of VAL pre-treatment. The decrease in CBF in the peripheral region of the ischemic area was significantly attenuated by pre-treatment with LCZ696 or VAL, without any significant effect on CBF in the core region. VAL or LCZ696 pre-treatment significantly decreased the increase of superoxide anion production in the cortex on the ischemic side. However, no significant difference in CBF and superoxide anion production was observed between VAL and LCZ696 pre-treatment. The preventive effect of LCZ696 on ischemic brain damage after stroke was more marked than that of VAL. LCZ696 could be used as a new approach to prevent brain damage after stroke. (246 words).
Copyright © 2015 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Angiotensin; Brain; Natriuretic peptide; Neprilysin; Stroke

Mesh:

Substances:

Year:  2015        PMID: 26057694     DOI: 10.1016/j.ejphar.2015.05.059

Source DB:  PubMed          Journal:  Eur J Pharmacol        ISSN: 0014-2999            Impact factor:   4.432


  10 in total

1.  LCZ696 (Sacubitril/valsartan) ameliorates oxidative stress, inflammation, fibrosis and improves renal function beyond angiotensin receptor blockade in CKD.

Authors:  Wanghui Jing; Nosratola D Vaziri; Ane Nunes; Yasunori Suematsu; Ted Farzaneh; Mahyar Khazaeli; Hamid Moradi
Journal:  Am J Transl Res       Date:  2017-12-15       Impact factor: 4.060

2.  Using Laser Doppler Imaging and Monitoring to Analyze Spinal Cord Microcirculation in Rat.

Authors:  Yingli Jing; Fan Bai; Hui Chen; Hao Dong
Journal:  J Vis Exp       Date:  2018-05-30       Impact factor: 1.355

Review 3.  Long-term neprilysin inhibition - implications for ARNIs.

Authors:  Duncan J Campbell
Journal:  Nat Rev Cardiol       Date:  2016-12-15       Impact factor: 32.419

4.  Sacubitril/Valsartan Decreases Cardiac Fibrosis in Left Ventricle Pressure Overload by Restoring PKG Signaling in Cardiac Fibroblasts.

Authors:  Ryan M Burke; Janet K Lighthouse; Deanne M Mickelsen; Eric M Small
Journal:  Circ Heart Fail       Date:  2019-04       Impact factor: 8.790

5.  Therapeutic Assessment of Combination Therapy with a Neprilysin Inhibitor and Angiotensin Type 1 Receptor Antagonist on Angiotensin II-Induced Atherosclerosis, Abdominal Aortic Aneurysms, and Hypertension.

Authors:  Yasir AlSiraj; Sean E Thatcher; Ching Ling Liang; Heba Ali; Mark Ensor; Lisa A Cassis
Journal:  J Pharmacol Exp Ther       Date:  2021-03-11       Impact factor: 4.030

Review 6.  From ARB to ARNI in Cardiovascular Control.

Authors:  Estrellita Uijl; Lodi C W Roksnoer; Ewout J Hoorn; A H Jan Danser
Journal:  Curr Hypertens Rep       Date:  2016-12       Impact factor: 5.369

7.  Combined Angiotensin Receptor-Neprilysin Inhibitors Improve Cardiac and Vascular Function Via Increased NO Bioavailability in Heart Failure.

Authors:  Rishi K Trivedi; David J Polhemus; Zhen Li; Daniel Yoo; Hiroshi Koiwaya; Amy Scarborough; Traci T Goodchild; David J Lefer
Journal:  J Am Heart Assoc       Date:  2018-03-03       Impact factor: 5.501

8.  Cardioprotective Effects of LCZ696 (Sacubitril/Valsartan) After Experimental Acute Myocardial Infarction.

Authors:  Masanobu Ishii; Koichi Kaikita; Koji Sato; Daisuke Sueta; Koichiro Fujisue; Yuichiro Arima; Yu Oimatsu; Tatsuro Mitsuse; Yoshiro Onoue; Satoshi Araki; Megumi Yamamuro; Taishi Nakamura; Yasuhiro Izumiya; Eiichiro Yamamoto; Sunao Kojima; Shokei Kim-Mitsuyama; Hisao Ogawa; Kenichi Tsujita
Journal:  JACC Basic Transl Sci       Date:  2017-12-25

9.  Neprilysin Inhibitor-Angiotensin II Receptor Blocker Combination Therapy (Sacubitril/valsartan) Suppresses Atherosclerotic Plaque Formation and Inhibits Inflammation in Apolipoprotein E- Deficient Mice.

Authors:  Hui Zhang; Gangqiong Liu; Wenping Zhou; Wenjing Zhang; Kai Wang; Jinying Zhang
Journal:  Sci Rep       Date:  2019-04-24       Impact factor: 4.379

Review 10.  Novel Therapeutic Approaches Targeting the Renin-Angiotensin System and Associated Peptides in Hypertension and Heart Failure.

Authors:  Lauren B Arendse; A H Jan Danser; Marko Poglitsch; Rhian M Touyz; John C Burnett; Catherine Llorens-Cortes; Mario R Ehlers; Edward D Sturrock
Journal:  Pharmacol Rev       Date:  2019-10       Impact factor: 25.468

  10 in total

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