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Published on: May 26, 2017
AMP-Activated Protein Kinase as a Reprogramming Strategy for Hypertension and Kidney Disease of Developmental Origin
You-Lin Tain1,2, Chien-Ning Hsu3
1Departments of Pediatrics, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung 833, Taiwan. tainyl@hotmail.com.
Abstract:
Suboptimal early-life conditions affect the developing kidney, resulting in long-term programming effects, namely renal programming. Adverse renal programming increases the risk for developing hypertension and kidney disease in adulthood. Conversely, reprogramming is a strategy aimed at reversing the programming processes in early life. AMP-activated protein kinase (AMPK) plays a key role in normal renal physiology and the pathogenesis of hypertension and kidney disease. This review discusses the regulation of AMPK in the kidney and provides hypothetical mechanisms linking AMPK to renal programming. This will be followed by studies targeting AMPK activators like metformin, resveratrol, thiazolidinediones, and polyphenols as reprogramming strategies to prevent hypertension and kidney disease. Further studies that broaden our understanding of AMPK isoform- and tissue-specific effects on renal programming are needed to ultimately develop reprogramming strategies. Despite the fact that animal models have provided interesting results with regard to reprogramming strategies targeting AMPK signaling to protect against hypertension and kidney disease with developmental origins, these results await further clinical translation.
Insights
Early life kidney programming can lead to adult hypertension and kidney disease. Activating AMP-activated protein kinase (AMPK) may offer a reprogramming strategy to prevent these conditions.
Area of Science:
- Nephrology
- Developmental programming
- Metabolic signaling
Background:
- Suboptimal early-life conditions can cause renal programming, increasing adult hypertension and kidney disease risk.
- AMP-activated protein kinase (AMPK) is crucial in kidney physiology and disease pathogenesis.
Purpose of the Study:
- To review AMPK regulation in the kidney and its link to renal programming.
- To explore AMPK activators as reprogramming strategies against hypertension and kidney disease.
Main Methods:
- Review of existing literature on AMPK, renal programming, and reprogramming strategies.
- Hypothetical mechanism development linking AMPK to renal programming.
- Discussion of studies on AMPK activators (metformin, resveratrol, etc.) for prevention.
Main Results:
- AMPK signaling pathways are implicated in renal programming.
- Several compounds (metformin, resveratrol, thiazolidinediones, polyphenols) show potential as AMPK-targeting reprogramming agents.
Conclusions:
- Targeting AMPK offers a promising strategy for reprogramming adverse early-life effects on the kidney.
- Further research on AMPK isoform-specific effects is needed for clinical translation of reprogramming strategies.
- Animal model findings require validation in human clinical trials.
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