Snake Venom Components as Therapeutic Drugs in Ischemic Heart Disease

Erij Messadi1

  • 1Plateforme de Physiologie et Physiopathologie Cardiovasculaires (P2C), Laboratoire des Biomolécules, Venins et Applications Théranostiques (LR20IPT01), Institut Pasteur de Tunis, Université Tunis El Manar, Tunis 1068, Tunisia.

Biomolecules
|October 28, 2023
PubMed

Insights

Snake venom toxins show promise for treating ischemic heart disease (IHD) and related conditions like hypertension. This review explores their molecular mechanisms and therapeutic potential for cardiovascular drug development.

Area of Science:

  • Cardiovascular Pharmacology
  • Toxicology
  • Drug Discovery

Background:

  • Ischemic heart disease (IHD), including myocardial infarction (MI), is a primary global cause of mortality.
  • While reperfusion limits MI size, it can worsen ischemic myocardial injury, highlighting the need for novel therapeutic strategies.
  • Snake venoms are a rich source of bioactive molecules with significant cardiovascular applications.

Purpose of the Study:

  • To review the potential of snake venom toxins in developing treatments for IHD.
  • To explore their application in managing related conditions such as hypertension and atherosclerosis.
  • To summarize their molecular mechanisms, pharmacological properties, and therapeutic targets.

Main Methods:

  • Literature review of existing research on snake venom toxins and cardiovascular diseases.
  • Analysis of biological effects at the molecular level.
  • Examination of pharmacological properties, mechanisms of action, and molecular pathways.

Main Results:

  • Snake venom-derived compounds, like captopril, have already led to successful cardiovascular drugs.
  • Various toxins exhibit diverse pharmacological activities relevant to IHD, hypertension, and atherosclerosis.
  • Molecules are in different stages of development, from approved drugs to preclinical candidates.

Conclusions:

  • Snake venom toxins represent a promising avenue for novel therapeutic agents against IHD.
  • Further research into these toxins can yield new drug candidates for cardiovascular diseases.
  • Understanding their molecular targets and pathways is crucial for effective drug development.

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