A new therapeutic target for the prevention of heart failure due to aortic stenosis

A new therapeutic target for the prevention of heart failure due to aortic stenosis
Cardiomyocyte-specific human β3AR overexpression prevents cardiomyocyte hypertrophy upon catecholamine challenge via NO/cGMP pathway. A Genetic constructs for adeno-associated virus (AAV) vectors encoding hβ3AR and control EGFP. ITR, recognition site for AVV packaging; Cmr4, enhancer sequence; Prom cTnT, troponin T promoter sequence for cardiomyocyte-specific expression; ADRB3, human β3AR receptor cDNA sequence, EGFP enhanced green fluorescent protein sequence, IRES internal ribosome entry site, Luciferase, firefly luciferase sequence; pA, simian virus 40 polyadenylation signal. B Representative images of neonatal rat ventricular myocytes (NRVM) transduced with control (AAV6-EGFP) or human β3AR adeno-associated virus (AAV6-hβ3AR) for 72 h and incubated for 24 h with isoproterenol (10 μM), L-NAME (100 μM) or both. Nucleus is stained in blue with DAPI and α-actin is stained in green to differentiate myocytes from other cells. Scale bar, 60 μm. C Size assessment of NVRM treated as above (40 cells/condition in each preparation; 3 independent preparations). The isoproterenol-induced hypertrophic response is blunted in hβ3AR myocytes and NOS inhibition by L-NAME restores the hypertrophy. D Confocal microscopy images of E9.5 cTnT+/+;R26ADRB3tg/tg (control) and cTnTCre/+;R26ADRB3tg/tg (c-hβ3tg) embryos, showing cardiac expression of GFP in an E9.5 embryo. E Immunoblot showing GFP expression in cardiomyocytes isolated from adult c-hβ3tg mice. F Immunostaining analysis for GFP in cardiac tissue. Scale bar, 50 µm. G β3AR protein levels is increased in c-hβ3tg mice. β3AR density (Bmax) in fmol of [3H]-CGP12177 specifically bound/ mg protein in homogenates from c-hβ3tg (red, n = 3) and WT (black, n = 3) hearts. H Mice with cardiomyocyte-specific overexpression of human β3AR (c-hβ3tg, red) and littermate controls (WT, black) were subjected to transaortic constriction (TAC) surgery (to induce supravalvular AS) or sham surgery and were followed for 2 weeks. I Supravalvular AS was confirmed by echocardiography as an increase in the descendant aortic velocity blood flow. J ATP levels were increased in hearts from c-hβ3tg 2 weeks after supravalvular AS induction (n = 5/condition). K Cyclic GMP:AMP levels ratio was boosted in hearts from c-hβ3tg mice, thus suggesting an enhancing effect of human β3 overexpression in cardiomyocytes on NO/cGMP signaling (n = 5/condition). Data are means ± SEM. Mann–Whitney or Student’s t test for non-normally or normally distributed data, and Kruskal–Wallis test with Dunn’s multiple comparisons test. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001. NS, not significant. Credit: Basic Research in Cardiology (2022). DOI: 10.1007/s00395-022-00966-z

Scientists at the Centro Nacional de Investigaciones Cardiovasculares (CNIC) have identified a new therapeutic target for the prevention of heart failure linked to aortic stenosis. The study was led by Dr. Borja Ibáñez, Clinical Research Director at the CNIC, cardiologist at Hospital Universitario Fundación Jiménez Díaz, and member of the Spanish cardiovascular research network (CiberCV).

The study shows that overexpression in cells of beta-3 , a member of the beta adrenergic system, can prevent or even reverse heart failure in a mouse model of , a condition that currently has few therapeutic options.

In the study, published in Basic Research in Cardiology, the CNIC team adopted an innovative approach to boost the expression of this receptor in the heart and thus reinforce its beneficial action.

"Gene therapy has an enormous potential for the treatment of cardiac diseases. The next step will be to investigate this approach in animals with a heart more similar to that of humans, such as pigs, and then design a pilot clinical trial to translate these promising results to patients," explained study co-author and CNIC General Director Dr. Valentín Fuster.

Aortic stenosis is a progressive narrowing of the aortic valve, a "floodgate" through which blood flows from the heart to the rest of the body. The progressive obstruction of the aortic valve impedes the supply of blood to the body organs and causes pressure to build within the heart. The extra force required to expel blood with each heartbeat generates a physical stress that deteriorates the . The condition is currently treated by replacing the damaged valve with a prosthesis.

While valve replacement technology has become much less invasive and successfully recovers valve function, Dr. Ibáñez explained that the cardiac muscle, after years of being subject to stress, does not recover. Unfortunately, there is a lack of treatments able to improve cardiac muscle function and thereby alleviate heart failure resulting from a long history of aortic stenosis.

In addition to the CNIC team led by Dr. Ibáñez's team, the study had input from groups based in Italy and the U.S.. The study exploited the beneficial properties of stimulating the beta-3 adrenergic receptor, which is abundant in adipose tissue and the bladder but weakly expressed in the heart. Previous research had shown that stimulation of this receptor, despite its low expression in the heart, has potentially beneficial effects on cardiac diseases.

Using rat heart muscle cells (cardiomyocytes) grown in culture, the researchers found that forced expression of beta-3 adrenergic receptor inhibited the hypertrophic growth of these cells when they were exposed to a hormonal stimulus.

Through a collaboration with the CNIC Intercellular Signaling in Cardiovascular Development and Disease group, led by Dr. Jose Luis de la Pompa, transgenic mice were generated that overexpress the beta-3 adrenergic receptor in cardiomyocytes.

"When these mice were subjected to supravalvular aortic stenosis, they developed less and fibrosis than mice with normal levels of expression. The transgenic mice were also free of heart failure, and their hearts were metabolically more efficient and consumed less glucose," explained Dr. Andrés Pun, first author on the study.

These results prompted the scientists to study the cardiomyocytes' mitochondria, the energy production hubs in cells. "Because heart muscle has such high energy requirements, any damage to its mitochondria can have catastrophic consequences, as frequently occurs in heart failure," said Dr. Pun.

In healthy hearts, mitochondria mainly burn fatty acids, which provide a highly efficient generation of abundant amounts of energy. Nevertheless, said Dr. Pun, "the failing heart often switches to the use of glucose, a much less efficient energy source, and this contributes to the progression of the disease."

In addition, the mitochondria of the failing heart are unable to fuse efficiently and are therefore smaller and more prone to accumulating injuries. The investigators found that the cardiomyocyte mitochondria in the transgenic mice were much larger and healthier.

Since the transgenic technology used to develop these mice is not applicable in patients, the investigators developed a gene therapy approach, whereby an innocuous virus was injected into mice to deliver the beta-3 adrenergic receptor gene specifically to cardiomyocytes, resulting in safe and efficient production of the receptor.

Working in partnership with the CNIC Viral Vectors Unit, the team designed an innocuous virus able to enter cardiomyocytes and drive elevated expression of beta-3 adrenergic receptor in the hearts of non-transgenic adult mice. When these mice were subjected to aortic stenosis, they were as equally protected against heart failure as transgenic mice overexpressing the receptor from before birth.

In a final test, the team injected the virus into non- with long-lasting aortic stenosis and established . In these mice, gene-therapy–induced overexpression of beta-3 adrenergic receptor recovered heart function, reduced cardiomyocyte hypertrophy, restored normal mitochondrial size and normal expression of mitochondrial fusion proteins in the heart, and increased animal survival.

More information: Andrés Pun-García et al, Beta-3 adrenergic receptor overexpression reverses aortic stenosis–induced heart failure and restores balanced mitochondrial dynamics, Basic Research in Cardiology (2022). DOI: 10.1007/s00395-022-00966-z

Provided by Centro Nacional de Investigaciones Cardiovasculares Carlos III (F.S.P.)
Citation: A new therapeutic target for the prevention of heart failure due to aortic stenosis (2022, November 30) retrieved 25 February 2024 from https://medicalxpress.com/news/2022-11-therapeutic-heart-failure-due-aortic.html
This document is subject to copyright. Apart from any fair dealing for the purpose of private study or research, no part may be reproduced without the written permission. The content is provided for information purposes only.

Explore further

Novel lncRNA 'Caren' counteracts heart failure progression


Feedback to editors