Implications of sodium hydrogen exchangers in various brain diseases.

Abstract

Na+/H+ exchangers (NHEs) are the transporter proteins that play an important role in intracellular pH (pHi) regulation, cell differentiation and cell volume and that mediate transepithelial Na+ and HCO3- absorption on the basis of chemical gradients across the plasma membrane. Its activation causes an increase in intracellular Na+, which further leads to Ca+ overload and cell death. The pharmacological inhibition of these transporter proteins prevents myocardial infarction and other heart diseases like congestive heart failure in experimental animal models as well as in clinical situations. The more recent studies have implicated the role of these exchangers in the pathophysiology of brain diseases. Out of nine NHE isoforms, NHE-1 is the major isoform present in the brain and regulates the trans-cellular ion transport through blood-brain barrier membrane, and alteration in their function leads to severe brain abnormalities. NHEs were shown to be involved in pathophysiologies of many brain diseases like epilepsy, Alzheimer's disease, neuropathic pain and ischemia/reperfusion-induced cerebral injury. Na+/H+-exchanger inhibitors (e.g., amiloride and cariporide) produce protective effects on ischemia/reperfusion-induced brain injury (e.g., stroke), exhibit good antiepileptic potential and attenuate neuropathic pain in various animal models. The present review focuses on the pathophysiological role of these ion exchangers in different brain diseases with possible mechanisms.

• Authors: Vivek Verma, Anjana Bali, Nirmal Singh, Amteshwar Singh Jaggi
• Journal: Journal of basic and clinical physiology and pharmacology (J Basic Clin Physiol Pharmacol) Vol. 26 Issue 5 Pg. 417-26 (Sep 2015) ISSN: 2191-0286 [Electronic] Germany
• PMID: 26020555 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Review)

Chemical References

• Sodium-Hydrogen Exchangers

Topics

• Animals
• Blood-Brain Barrier (metabolism)
• Brain Diseases (metabolism, pathology)
• Humans
• Sodium-Hydrogen Exchangers (metabolism)