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Insulin-like growth factor-1 signaling in cardiac aging
1Division of Cardiology, Department of Internal Medicine, College of Medicine, Chung-Ang University, Seoul, Republic of Korea.
Insights
Cardiovascular aging is linked to the Insulin-like Growth Factor-1 (IGF-1)/IGF-1 Receptor (IGF-1R) system. Deleting IGF-1R in aged mice hearts may delay age-related cardiac dysfunction.
Area of Science:
- Cardiovascular research
- Aging biology
- Molecular medicine
Background:
- Cardiovascular disease (CVD) is a primary cause of mortality, with aging as a significant risk factor.
- The Insulin-like Growth Factor-1 (IGF-1) system, including its receptor (IGF-1R), plays a crucial role in cellular processes and is implicated in cardiac aging and longevity.
- Cardiac aging involves intrinsic dysfunction and molecular/cellular alterations.
Purpose of the Study:
- To review the current understanding of the IGF-1/IGF-1R system's role in cardiac aging.
- To compare the biological effects of IGF-1R and the insulin receptor.
- To present findings on the impact of cardiomyocyte-specific IGF-1R deletion in aged mice on senescence-associated myocardial pathologies.
Main Methods:
- Literature review of studies on IGF-1/IGF-1R signaling in cardiac aging.
- Comparative analysis of IGF-1R and insulin receptor functions.
- Examination of data from aged knockout mice with cardiomyocyte-specific IGF-1R deletion.
Main Results:
- The IGF-1/IGF-1R signaling pathway is a key regulator of cardiac aging.
- IGF-1R and insulin receptor exhibit distinct yet overlapping biological effects.
- Deletion of IGF-1R in aged cardiomyocytes can mitigate the development of age-related myocardial pathologies.
Conclusions:
- The IGF-1/IGF-1R system is a critical determinant of cardiac aging.
- Targeting IGF-1R in cardiomyocytes presents a potential therapeutic strategy for age-related cardiac dysfunction.
- Further research into the comparative roles of IGF-1R and insulin receptor could yield novel insights into cardiovascular health during aging.
Abstract:
Cardiovascular disease (CVD) is the leading cause of death in most developed countries. Aging is associated with enhanced risk of CVD. Insulin-like growth factor-1 (IGF-1) binds to its cognate receptor, IGF-1 receptor (IGF-1R), and exerts pleiotropic effects on cell growth, differentiation, development, and tissue repair. Importantly, IGF-1/IGF-1R signaling is implicated in cardiac aging and longevity. Cardiac aging is an intrinsic process that results in cardiac dysfunction, accompanied by molecular and cellular changes. In this review, we summarize the current state of knowledge regarding the link between the IGF-1/IGF-1R system and cardiac aging. The biological effects of IGF-1R and insulin receptor will be discussed and compared. Furthermore, we describe data regarding how deletion of IGF-1R in cardiomyocytes of aged knockout mice may delay the development of senescence-associated myocardial pathologies. This article is part of a Special issue entitled Cardiac adaptations to obesity, diabetes and insulin resistance, edited by Professors Jan F.C. Glatz, Jason R.B. Dyck and Christine Des Rosiers.
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