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• W2150393025 endingPage "333" @default.
• W2150393025 startingPage "313" @default.
• W2150393025 abstract "Tachykinins (also known as neurokinins) share a common C-terminal sequence, Phe-X-Gly-Leu-Met-NH2 (where X is Phe, Tyr, Val or Ile). Substance P was the first to be discovered and is the best characterised. Other tachykinins notable for their widespread distribution in mammalian tissues, including the peripheral and central nervous system, are neurokinins A and B. The biological actions of tachykinins are through G-protein linked receptors designated NK1, NK2 and NK3 and there has been an assumption that the preferred agonists were substance P, neurokinin A and neurokinin B respectively [1], [2]. However, the receptor selectivity of these peptides is relatively poor. There is a mismatch between tachykinin-containing neurones and fibres and their corresponding receptor in certain brain regions and this is particularly apparent in the case of neurokinin A since NK2 receptor expression appears to be extremely low in the adult mammalian nervous system [3]. A novel NK4 receptor has been proposed and it appears that there are two NK3 receptors designated A and B [4]." @default.
• W2150393025 created "2016-06-24" @default.
• W2150393025 creator A5036161330 @default.
• W2150393025 creator A5069068117 @default.
• W2150393025 date "1999-01-01" @default.
• W2150393025 modified "2023-09-26" @default.
• W2150393025 title "Tachykinin receptors and the potential of tachykinin antagonists as clinically effective analgesics and anti-inflammatory agents" @default.
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