4.2 Review

Calcitonin gene-related peptide (CGRP) and its role in hypertension

期刊

NEUROPEPTIDES
卷 45, 期 2, 页码 93-104

出版社

CHURCHILL LIVINGSTONE
DOI: 10.1016/j.npep.2010.12.002

关键词

CGRP; Hypertension; Sensory nerves; Human; Mouse; Rat; CLR; RAMP1; TRPV1

资金

  1. BBSRC
  2. BPS
  3. HEFCE
  4. KTN
  5. MRC
  6. SFC
  7. Biotechnology and Biological Sciences Research Council [BB/E527098/1] Funding Source: researchfish
  8. BBSRC [BB/E527098/1] Funding Source: UKRI

向作者/读者索取更多资源

Hypertension is still presently the number one silent killer in the Western World, and a major risk factor for the development of secondary diseases contributing to cardiovascular disease (CVD). However, despite a broad range of therapies, the mechanisms involved in the onset of hypertension remains unclear, therefore there is a real need to investigate the mechanisms involved. Calcitonin gene-related peptide (CGRP) is the most potent microvascular vasodilator known to date. Widely expressed in the nervous system, this peptide is considered to play a positive role in wound healing and protects against ischaemic and other traumas. However, whilst the protective mechanisms are not well understood, evidence indicates that these mechanisms become important in vascular-related stress. This review provides evidence that CGRP is both a potent vasodilator and hypotensive agent. However studies to date suggest that CGRP does not contribute to the physiological regulation of blood pressure. By comparing results from a range of human and animal studies, findings broadly suggest an association between CGRP and the pathophysiology of hypertension in terms of protective mechanisms, with possibly the RAMP1 component of the CGRP receptor playing a key role in the brain stem, in addition to peripheral receptors. The studies of agents that release CGRP agonists are at an early stage, with analogues for human use currently under development. However, at this stage, further research is required to establish the mechanisms by which CGRP is protective in the onset of hypertension, if novel and therapeutic modes of treatment are to be developed. (C) 2011 Elsevier Ltd. All rights reserved.

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