Tachykinin peptides

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Overview[edit | edit source]

Structure of a tachykinin peptide.

Tachykinin peptides are a family of neuropeptides that share a common C-terminal sequence and are involved in a variety of physiological processes. These peptides are characterized by their ability to rapidly induce contraction of smooth muscle tissues, hence the name "tachykinin," derived from the Greek words "tachys" (swift) and "kinein" (to move).

Structure[edit | edit source]

Tachykinins are small peptides, typically consisting of 10-12 amino acids. The defining feature of tachykinins is their conserved C-terminal sequence, which is -Phe-X-Gly-Leu-Met-NH2, where "X" can be various amino acids. This sequence is crucial for their biological activity and interaction with neurokinin receptors.

Function[edit | edit source]

Tachykinins are involved in numerous physiological functions, including:

Types of Tachykinins[edit | edit source]

The most well-known tachykinins include:

Receptors[edit | edit source]

Tachykinins exert their effects by binding to specific G protein-coupled receptors known as neurokinin receptors. There are three main types of neurokinin receptors:

Clinical Significance[edit | edit source]

Tachykinins and their receptors are targets for therapeutic interventions in various conditions, such as:

  • Chronic pain: Antagonists of the NK1 receptor are used to manage pain.
  • Asthma and COPD: Tachykinin receptor antagonists can help reduce bronchoconstriction.
  • Depression and anxiety: NK1 receptor antagonists are being explored for their potential antidepressant and anxiolytic effects.

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