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Published on: June 27, 2022
Preventing Developmental Origins of Cardiovascular Disease: Hydrogen Sulfide as a Potential Target?
Chien-Ning Hsu1,2, You-Lin Tain3,4
1Department of Pharmacy, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung 833, Taiwan.
Insights
Early-life insults can program cardiovascular disease (CVD). Hydrogen sulfide (H2S) interventions show promise in preventing adult-onset CVD by reprogramming these developmental origins.
Area of Science:
- Cardiovascular physiology
- Developmental biology
- Biochemistry
Background:
- Cardiovascular disease (CVD) can arise from early-life insults, a concept known as the developmental origins of health and disease (DOHaD).
- Hydrogen sulfide (H2S), a key regulator of cardiovascular homeostasis, is implicated in the pathogenesis of developmental origins of CVD.
- Early interventions using H2S have shown potential in preventing adult-onset CVD in animal models through reprogramming.
Purpose of the Study:
- To review the current understanding of H2S in cardiovascular programming.
- To explore the mechanisms linking H2S signaling to cardiovascular programming.
- To summarize H2S-based reprogramming strategies for preventing developmental origins of CVD.
Main Methods:
- Literature review focusing on H2S, cardiovascular programming, and DOHaD.
- Analysis of evidence linking H2S signaling pathways to CVD mechanisms.
- Overview of animal studies on H2S-based interventions for CVD prevention.
Main Results:
- H2S plays a dual role in cardiovascular programming, acting pathologically in developmental origins of CVD and therapeutically via reprogramming.
- Mechanisms include modulation of oxidative stress, nitric oxide, nutrient sensing, renin-angiotensin system, and gut microbiota.
- H2S precursors and donors demonstrate preventative effects against adult-onset CVD in animal models.
Conclusions:
- Understanding H2S's role in cardiovascular programming is crucial for developing novel CVD prevention strategies.
- H2S-based reprogramming interventions offer a promising therapeutic avenue for mitigating the global burden of CVD.
- Further research into H2S signaling and interventions could lead to effective strategies for preventing adult-onset cardiovascular diseases originating in early life.
Abstract:
The cardiovascular system can be programmed by a diversity of early-life insults, leading to cardiovascular disease (CVD) in adulthood. This notion is now termed developmental origins of health and disease (DOHaD). Emerging evidence indicates hydrogen sulfide (H2S), a crucial regulator of cardiovascular homeostasis, plays a pathogenetic role in CVD of developmental origins. Conversely, early H2S-based interventions have proved beneficial in preventing adult-onset CVD in animal studies via reversing programming processes by so-called reprogramming. The focus of this review will first summarize the current knowledge on H2S implicated in cardiovascular programming. This will be followed by supporting evidence for the links between H2S signaling and underlying mechanisms of cardiovascular programming, such as oxidative stress, nitric oxide deficiency, dysregulated nutrient-sensing signals, activation of the renin-angiotensin system, and gut microbiota dysbiosis. It will also provide an overview from animal models regarding how H2S-based reprogramming interventions, such as precursors of H2S and H2S donors, may prevent CVD of developmental origins. A better understanding of cardiovascular programming and recent advances in H2S-based interventions might provide the answers to bring down the global burden of CVD.
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