AI Article Synopsis

  • The kidneys filter toxins and regulate osmotic pressure but undergo significant changes with aging, leading to challenges in identifying age-related disorders as life expectancy increases.* -
  • Structural alterations in the kidneys are linked to changes in specific proteins and epigenetic factors, which play critical roles in renal health and can indicate acute kidney injury (AKI).* -
  • Hydrogen sulfide (HS) shows potential benefits in treating kidney injuries by reducing inflammation and oxidative stress; however, its mechanisms and effects need further research to fully understand its role in renal healing.*

Article Abstract

The kidney is an essential excretory organ that works as a filter of toxins and metabolic by-products of the human body and maintains osmotic pressure throughout life. The kidney undergoes several physiological, morphological, and structural changes with age. As life expectancy in humans increases, cell senescence in renal aging is a growing challenge. Identifying age-related kidney disorders and their cause is one of the contemporary public health challenges. While the structural abnormalities to the extracellular matrix (ECM) occur, in part, due to changes in MMPs, EMMPRIN, and Meprin-A, a variety of epigenetic modifiers, such as DNA methylation, histone alterations, changes in small non-coding RNA, and microRNA (miRNA) expressions are proven to play pivotal roles in renal pathology. An aged kidney is vulnerable to acute injury due to ischemia-reperfusion, toxic medications, altered matrix proteins, systemic hemodynamics, etc., non-coding RNA and miRNAs play an important role in renal homeostasis, and alterations of their expressions can be considered as a good marker for AKI. Other epigenetic changes, such as histone modifications and DNA methylation, are also evident in AKI pathophysiology. The endogenous production of gaseous molecule hydrogen sulfide (HS) was documented in the early 1980s, but its ameliorative effects, especially on kidney injury, still need further research to understand its molecular mode of action in detail. HS donors heal fibrotic kidney tissues, attenuate oxidative stress, apoptosis, inflammation, and GFR, and also modulate the renin-angiotensin-aldosterone system (RAAS). In this review, we discuss the complex pathophysiological interplay in AKI and its available treatments along with future perspectives. The basic role of HS in the kidney has been summarized, and recent references and knowledge gaps are also addressed. Finally, the healing effects of HS in AKI are described with special emphasis on epigenetic regulation and matrix remodeling.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11429536PMC
http://dx.doi.org/10.3390/biom14091165DOI Listing

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