Literature DB >> 24269214

N-acylhydrazone improves exercise intolerance in rats submitted to myocardial infarction by the recovery of calcium homeostasis in skeletal muscle.

Jaqueline Soares da Silva1, Sharlene Lopes Pereira1, Rodolfo do Couto Maia1, Sharon Schilling Landgraf2, Celso Caruso-Neves2, Arthur Eugen Kümmerle3, Carlos Alberto Manssour Fraga1, Eliezer Jesus Barreiro1, Roberto Takashi Sudo1, Gisele Zapata-Sudo4.   

Abstract

AIMS: This work investigated the effects of 3,4-methylenedioxybenzoyl-2-thienylhydrazone (LASSBio-294) treatment on the contractile response of soleus (SOL) muscle from rats submitted to myocardial infarction (MI). MAIN
METHODS: Following coronary artery ligation, LASSBio-294 (2mg/kg, i.p.) or vehicle was administrated once daily for 4 weeks. KEY
FINDINGS: The run time to fatigue for sham rats was 17.9 ±2.6 min, and it was reduced to 3.3 ± 0.8 min (P<0.05) in MI rats. In MI rats treated with LASSBio-294, the time to fatigue was 15.1 ± 3.6 min. During the contractile test, SOL muscles from sham rats showed a response of 7.12 ± 0.54N/cm(2) at 60 Hz, which was decreased to 5.45 ± 0.49 N/cm(2) (P<0.05) in MI rats. The contractility of SOL muscles from the MI-LASSBio-294 group was increased to 9.01 ± 0.65N/cm(2). At 16 mM caffeine, the contractility was reduced from 2.31 ± 0.33 to 1.60 ± 0.21 N/cm(2) (P<0.05) in the MI group. In SOL muscles from MI-LASSBio-294 rats, the caffeine response was increased to 2.62 ± 0.33 N/cm(2). Moreover, SERCA2a expression in SOL muscles was decreased by 0.31-fold (31%) in the MI group compared to the Sham group (P<0.05). In the MI-LASSBio-294 group, it was increased by 1.53-fold (153%) compared to the MI group (P<0.05). Meanwhile, the nuclear density in SOL muscles was increased in the MI group compared to the Sham group. Treatment with LASSBio-294 prevented this enhancement of cellular infiltrate. SIGNIFICANCE: LASSBio-294 treatment prevented the development of muscular fatigue and improved exercise intolerance in rats submitted to MI.
Copyright © 2014 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Exercise intolerance; LASSBio-294; Myocardial infarction; SERCA2a expression

Mesh:

Substances:

Year:  2013        PMID: 24269214     DOI: 10.1016/j.lfs.2013.11.012

Source DB:  PubMed          Journal:  Life Sci        ISSN: 0024-3205            Impact factor:   5.037


  4 in total

1.  Cardioprotection Induced by Activation of GPER in Ovariectomized Rats With Pulmonary Hypertension.

Authors:  Allan K N Alencar; Guilherme C Montes; Daniele G Costa; Luiza V P Mendes; Ananssa M S Silva; Sabrina T Martinez; Margarete M Trachez; Valéria do M N Cunha; Tadeu L Montagnoli; Aline G M Fraga; Hao Wang; Leanne Groban; Carlos A M Fraga; Roberto T Sudo; Gisele Zapata-Sudo
Journal:  J Gerontol A Biol Sci Med Sci       Date:  2018-08-10       Impact factor: 6.053

Review 2.  Adenosine Receptors As Drug Targets for Treatment of Pulmonary Arterial Hypertension.

Authors:  Allan K N Alencar; Guilherme C Montes; Eliezer J Barreiro; Roberto T Sudo; Gisele Zapata-Sudo
Journal:  Front Pharmacol       Date:  2017-12-04       Impact factor: 5.810

3.  Adenosine A2A receptor agonist prevents cardiac remodeling and dysfunction in spontaneously hypertensive male rats after myocardial infarction.

Authors:  Jaqueline S da Silva; Daniele Gabriel-Costa; Roberto T Sudo; Hao Wang; Leanne Groban; Emanuele B Ferraz; José Hamilton M Nascimento; Carlos Alberto M Fraga; Eliezer J Barreiro; Gisele Zapata-Sudo
Journal:  Drug Des Devel Ther       Date:  2017-03-06       Impact factor: 4.162

4.  Effect of S-Se Bioisosteric Exchange on Affinity and Intrinsic Efficacy of Novel N-acylhydrazone Derivatives at the Adenosine A2A Receptor.

Authors:  Júlia Galvez Bulhões Pedreira; Rafaela Ribeiro Silva; François G Noël; Eliezer J Barreiro
Journal:  Molecules       Date:  2021-12-04       Impact factor: 4.411

  4 in total

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