Neuroprotective Effects of Drug-Induced Therapeutic Hypothermia in Central Nervous System Diseases

Curr Drug Targets. 2017;18(12):1392-1398. doi: 10.2174/1389450118666170607104251.

Abstract

Objective: This review article focuses on the neuroprotective effect of drug-induced hypothermia in cerebrovascular diseases and discusses its related side effects.

Method: A systematic literature search was performed using Pubmed and Embase electronic databases for a retrospective analysis.

Results: Experimental studies have shown that drug-induced hypothermia alleviates brain damage and plays a neuroprotective role, thereby reducing mortality and ameliorating neurological deficits. Therefore, drug-induced hypothermia has an important research value and is worth further consideration in the clinical setting. However, drug-induced hypothermia is also associated with side effects, such as ventricular tachycardia, ventricular fibrillation, suppressed immune function, infection, electrolyte imbalance, glucose metabolism disorders, and skeletal muscle tremor. Existing drugs with cooling effects belong to the following categories: (1) dopamine receptor agonists; (2) cannabis; (3) opioid receptors; (4) vanilloid receptors; (5) vasopressins (potent neurotensin receptor agonists); (6) thyroid drugs; (7) adenosine drugs; and (8) purine drugs.

Keywords: Drug-induced therapeutic hypothermia; cerebral ischemia; cerebral hemorrhage; cerebrovascular diseases; neuroprotection.

Publication types

  • Review

MeSH terms

  • Animals
  • Cannabis / adverse effects
  • Central Nervous System Diseases / therapy*
  • Dopamine Agonists / administration & dosage
  • Dopamine Agonists / adverse effects
  • Humans
  • Hypothermia, Induced / adverse effects*
  • Hypothermia, Induced / methods
  • Neuroprotective Agents / administration & dosage*
  • Neuroprotective Agents / adverse effects
  • Receptors, Opioid / administration & dosage
  • Retrospective Studies
  • TRPV Cation Channels / administration & dosage
  • TRPV Cation Channels / adverse effects
  • Vasopressins / agonists

Substances

  • Dopamine Agonists
  • Neuroprotective Agents
  • Receptors, Opioid
  • TRPV Cation Channels
  • Vasopressins