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Time course of decompensation after angiotensin II and high-salt diet in Balb/CJ mice suggests pulmonary hypertension-induced cardiorenal syndrome

Becirovic-Agic, Mediha (författare)
Uppsala universitet,Integrativ Fysiologi
Jönsson, Sofia (författare)
Uppsala universitet,Integrativ Fysiologi
Tveitarås, Maria K. (författare)
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Skogstrand, Trude (författare)
Karlsen, Tine, V (författare)
Lidén, Åsa (författare)
Leh, Sabine (författare)
Ericsson, Madelene (författare)
Umeå universitet,Fysiologisk kemi
Nilsson, Stefan K., 1979- (författare)
Umeå universitet,Fysiologisk kemi
Reed, Rolf K. (författare)
Hultström, Michael, 1978- (författare)
Uppsala universitet,Anestesiologi och intensivvård,Integrativ Fysiologi,Department of Biomedicine, University of Bergen, Bergen, Norway
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 (creator_code:org_t)
the American Physiological Society, 2019
2019
Engelska.
Ingår i: American Journal of Physiology. Regulatory Integrative and Comparative Physiology. - : the American Physiological Society. - 0363-6119 .- 1522-1490. ; 316:5, s. R563-R570
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • The genetic background of a mouse strain determines its susceptibility to disease. C57BL/6J and Balb/CJ are two widely used inbred mouse strains that we found react dramatically differently to angiotensin II and high-salt diet (ANG II + Salt). Balb/CJ show increased mortality associated with anuria and edema formation while C57BL/6J develop arterial hypertension but do not decompensate and die. Clinical symptoms of heart failure in Balb/CJ mice gave the hypothesis that ANG II + Salt impairs cardiac function and induces cardiac remodeling in male Balb/CJ but not in male C57BL/6J mice. To test this hypothesis, we measured cardiac function using echocardiography before treatment and every day for 7 days during treatment with ANG II + Salt. Interestingly, pulsed wave Doppler of pulmonary artery flow indicated increased pulmonary vascular resistance and right ventricle systolic pressure in Balb/CJ mice, already 24 h after ANG II + Salt treatment was started. In addition, Balb/CJ mice showed abnormal diastolic filling indicated by reduced early and late filling and increased isovolumic relaxation time. Furthermore, Balb/CJ exhibited lower cardiac output compared with C57BL/6J even though they retained more sodium and water, as assessed using metabolic cages. Left posterior wall thickness increased during ANG II + Salt treatment but did not differ between the strains. In conclusion, ANG II + Salt treatment causes early restriction of pulmonary flow and reduced left ventricular filling and cardiac output in Balb/CJ, which results in fluid retention and peripheral edema. This makes Balb/CJ a potential model to study the adaptive capacity of the heart for identifying new disease mechanisms and drug targets.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Fysiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Physiology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Kardiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cardiac and Cardiovascular Systems (hsv//eng)

Nyckelord

animal model
congestive heart failure
pulmonary hypertension
right-sided heart failure

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