Literature DB >> 19817931

Age-related increase in atrial fibrillation induced by transvenous catheter-based atrial burst pacing: an in vivo rat model of inducible atrial fibrillation.

Dongzhu Xu1, Nobuyuki Murakoshi, Hiroshi Tada, Miyako Igarashi, Yukio Sekiguchi, Kazutaka Aonuma.   

Abstract

INTRODUCTION: Large animal models of atrial fibrillation (AF) are well established, but limited experimental reports exist on small animal models. We sought to develop an in vivo rat model of AF using a transvenous catheter and to evaluate the model's underlying characteristics. METHODS AND
RESULTS: Echocardiogram, surface electrocardiogram (ECG), and atrial effective refractory period (AERP) were recorded at baseline in young (3 months) and middle-aged (9 months) Wistar rats. AF inducibility and duration were measured through transvenous electrode catheter in young (n = 11) and middle-aged rats (n = 11) and middle-aged rats treated with either pilsicainide (1 mg/kg iv, n = 7) or amiodarone (10 mg/kg iv, n = 9). Degrees of interstitial fibrosis and cellular hypertrophy in the atria were assessed histologically. The P-wave duration and AERP were significantly longer and echocardiographic left atrial dimension significantly larger in middle-aged versus young rats. AF was inducible in >90% of all procedures in both untreated rat groups, whereas AF inducibility was reduced by the antiarrhythmic drugs. The AF duration was significantly longer in middle-aged than in young rats and was significantly shortened by treatment with either pilsicainide or amiodarone. Histologic analysis revealed significant increases in atrial interstitial fibrosis and cellular diameter in middle-aged versus young rats.
CONCLUSIONS: Transvenous catheter-based AF is significantly longer in middle-aged than in young rats and is markedly reduced by treatment with antiarrhythmic drugs. This rat model of AF is simple, reproducible, and reliable for examining pharmacologic effects on AF and studying the process of atrial remodeling.

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Year:  2009        PMID: 19817931     DOI: 10.1111/j.1540-8167.2009.01591.x

Source DB:  PubMed          Journal:  J Cardiovasc Electrophysiol        ISSN: 1045-3873


  6 in total

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Journal:  Pflugers Arch       Date:  2010-06-16       Impact factor: 3.657

2.  Cardiac overexpression of perilipin 2 induces atrial steatosis, connexin 43 remodeling, and atrial fibrillation in aged mice.

Authors:  Satsuki Sato; Jinya Suzuki; Masamichi Hirose; Mika Yamada; Yasuo Zenimaru; Takahiro Nakaya; Mai Ichikawa; Michiko Imagawa; Sadao Takahashi; Shoichiro Ikuyama; Tadashi Konoshita; Fredric B Kraemer; Tamotsu Ishizuka
Journal:  Am J Physiol Endocrinol Metab       Date:  2019-10-29       Impact factor: 4.310

3.  Aerobic Interval Training Prevents Age-Dependent Vulnerability to Atrial Fibrillation in Rodents.

Authors:  Vegard Malmo; Allen Kelly; Karin S Garten; Tomas Stolen; Natale P L Rolim; Ulrik Wisloff; Godfrey Smith; Jan P Loennechen
Journal:  Front Physiol       Date:  2018-03-09       Impact factor: 4.566

4.  Nicotinamide Phosphoribosyltransferase (Nampt)/Nicotinamide Adenine Dinucleotide (NAD) Axis Suppresses Atrial Fibrillation by Modulating the Calcium Handling Pathway.

Authors:  Duo Feng; DongZhu Xu; Nobuyuki Murakoshi; Kazuko Tajiri; Rujie Qin; Saori Yonebayashi; Yuta Okabe; Siqi Li; Zixun Yuan; Kazutaka Aonuma; Masaki Ieda
Journal:  Int J Mol Sci       Date:  2020-06-30       Impact factor: 5.923

5.  Atrial fibrillation and its arrhythmogenesis associated with insulin resistance.

Authors:  Yi-Hsin Chan; Gwo-Jyh Chang; Ying-Ju Lai; Wei-Jan Chen; Shang-Hung Chang; Li-Man Hung; Chi-Tai Kuo; Yung-Hsin Yeh
Journal:  Cardiovasc Diabetol       Date:  2019-09-26       Impact factor: 9.951

6.  Modulation of miR-10a-mediated TGF-β1/Smads signaling affects atrial fibrillation-induced cardiac fibrosis and cardiac fibroblast proliferation.

Authors:  Peng-Fei Li; Rong-Hua He; Shao-Bo Shi; Rui Li; Qiong-Tao Wang; Guo-Tao Rao; Bo Yang
Journal:  Biosci Rep       Date:  2019-02-08       Impact factor: 3.840

  6 in total

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