A Model of Left Ventricular Dysfunction Complicated by CAWS Arteritis in DBA/2 Mice
Author(s) -
Naoto Hirata,
Kenichi Ishibashi,
Tatsuya Usui,
Jiro Yoshioka,
Satoru Hata,
Yoshiyuki Adachi,
Noriko NagiMiura,
Shin Ohta,
Naohito Ohno
Publication year - 2012
Publication title -
international journal of vascular medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.411
H-Index - 27
eISSN - 2090-2832
pISSN - 2090-2824
DOI - 10.1155/2012/570297
Subject(s) - medicine , arteritis , ventricular outflow tract , cardiology
It was reported previously that a Candida albicans water-soluble fraction (CAWS), including a mannoprotein and β -glucan complex, has strong potency in inducing fatal necrotizing arteritis in DBA/2 mice. In this study, histopathological changes and cardiac function were investigated in this system. One mg/day of CAWS was given to DBA/2 mice via peritoneal injection for five days. The CAWS-treated DBA/2 mice were induced aortitis and died at an incidence of 100% within several weeks. Histological findings included stenosis in the left ventricular outflow tract (LVOT) and severe inflammatory changes of the aortic valve with fibrinoid necrosis. Cardiomegaly was observed and heart weight increased 1.62 fold ( P < 0.01). Echocardiography revealed a severe reduction in contractility and dilatation of the cavity in the left ventricle (LV): LV fractional shortening (LVFS) decreased from 71% to 38% ( P < 0.01), and the LV end-diastolic diameter (LVDd) increased from 2.21 mm to 3.26 mm ( P < 0.01). The titer of BNP mRNA increased in the CAWS-treated group. Severe inflammatory changes resulting from CAWS brought about lethal LV dysfunction by aortic valve deformation with LVOT stenosis. This system is proposed as an easy and useful experimental model of heart failure because CAWS arteritis can be induced by CAWS injection alone.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom