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Immunology, Endocrine & Metabolic Agents in Medicinal Chemistry (Discontinued)


ISSN (Print): 1871-5222
ISSN (Online): 1875-6115

Clarithromycin Attenuates Left Ventricular Remodeling and Dysfunction after Pressure Overload in Mice

Author(s): Risako Yamada, Jun-Ichi Suzuki, Masahito Ogawa, Ryo Watanabe and Mitsuaki Isobe

Volume 12, Issue 2, 2012

Page: [147 - 151] Pages: 5

DOI: 10.2174/187152212800388978

Price: $65


Background: Left ventricular (LV) hypertrophy is a natural adaption of the heart to pressure overloading and results in life-threatening heart failure. Matrix metalloproteinase (MMP) activity is upregulated in hearts with LV hypertrophy and its activation is the main cause of change in the LV wall. Clarithromycin (CAM), a major macrolide antibiotic, has various biologic effects including MMP regulation. However, little is known about the effect of CAM on LV hypertrophy.

Methods and Results: To clarify the role of CAM on LV hypertrophy, we used the transverse aortic constriction (TAC) model. The mice were randomly assigned into three groups; (a) CAM administration with TAC (CAM-treated group, n=10); (b) vehicle administration with TAC (non-treated group, n=10); (c) vehicle administration with sham-operation (control group, n=10). M-mode echocardiograms showed that LV end-diastolic posterior wall (LVPWd) thickness increased progressively from week 1 to 3 after TAC in the non-treated group. However, it was attenuated in the CAMtreated group. Furthermore, heart to body weight ratio increased in the non-treated group (15.8±1.7%); this increase was negated by CAM administration (10.2±1.4%). Histpathologically, LV wall thickness increased in the non-treated group (18.0±4.0%); this increase was also negated in the CAM-treated group (-8.5±3.5%). Real-time RT-PCR demonstrated that CAM treatment tended to suppress MMP-9 and elevate TIMP-2 mRNA levels compared to the non-treated group.

Conclusion: CAM attenuates the progression of LV hypertrophy via MMP suppression after pressure overload in mice. It might be a basic solution for LV hypertrophy.

Keywords: Clarithromycin, clarithromycin, extracellular matrix, echocardiograms, heart, fibrosis, macrolide antibiotic, matrix metalloproteinase, mice, pressure overload, pathology, polymerase chain reaction, transverse aortic constriction, ventricular hypertrophy

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