Protective Roles of Hydrogen Sulfide in Alzheimer’s Disease and Traumatic Brain Injury

Author:

Paul Bindu D.1234ORCID,Pieper Andrew A.567891011

Affiliation:

1. Department of Pharmacology and Molecular Sciences, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA

2. The Solomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA

3. Department of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA

4. Lieber Institute for Brain Development, Baltimore, MD 21205, USA

5. Brain Health Medicines Center, Harrington Discovery Institute, University Hospitals Cleveland Medical Center, Cleveland, OH 44106, USA

6. Department of Psychiatry, Case Western Reserve University, Cleveland, OH 44106, USA

7. Geriatric Psychiatry, GRECC, Louis Stokes Cleveland VA Medical Center, Cleveland, OH 44106, USA

8. Institute for Transformative Molecular Medicine, School of Medicine, Case Western Reserve University, Cleveland, OH 44106, USA

9. Department of Pathology, Case Western Reserve University, School of Medicine, Cleveland, OH 44106, USA

10. Department of Neuroscience, Case Western Reserve University, School of Medicine, Cleveland, OH 44106, USA

11. Translational Therapeutics Core, Cleveland Alzheimer’s Disease Research Center, Cleveland, OH 44106, USA

Abstract

The gaseous signaling molecule hydrogen sulfide (H2S) critically modulates a plethora of physiological processes across evolutionary boundaries. These include responses to stress and other neuromodulatory effects that are typically dysregulated in aging, disease, and injury. H2S has a particularly prominent role in modulating neuronal health and survival under both normal and pathologic conditions. Although toxic and even fatal at very high concentrations, emerging evidence has also revealed a pronounced neuroprotective role for lower doses of endogenously generated or exogenously administered H2S. Unlike traditional neurotransmitters, H2S is a gas and, therefore, is unable to be stored in vesicles for targeted delivery. Instead, it exerts its physiologic effects through the persulfidation/sulfhydration of target proteins on reactive cysteine residues. Here, we review the latest discoveries on the neuroprotective roles of H2S in Alzheimer’s disease (AD) and traumatic brain injury, which is one the greatest risk factors for AD.

Funder

American Heart Association and Paul Allen Foundation

NIH NIDA

Solve-ME foundation

Catalyst Award from Johns Hopkins University

Case Western Reserve University

University Hospitals Morley-Mather Chair in Neuropsychiatry

The Valour Foundation

Brockman Foundation

Department of Veterans Affairs Merit Award

Translational Therapeutics Core of the Cleveland Alzheimer’s Disease Research Center

Elizabeth Ring Mather & William Gwinn Mather Fund

S. Livingston Samuel Mather Trust

G.R. Lincoln Family Foundation

Wick Foundation

Leonard Krieger Fund of the Cleveland Foundation

Maxine and Lester Stoller Parkinson’s Research Fund

Louis Stokes VA Medical Center resources and facilities

Publisher

MDPI AG

Subject

Cell Biology,Clinical Biochemistry,Molecular Biology,Biochemistry,Physiology

Reference158 articles.

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5. Role of transamination and pyridoxal phosphate in the enzymatic formation of hydrogen sulfide from cysteine by the rat liver under anaerobiosis;Chatagner;Bull. Soc. Chim. Biol.,1956

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