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降钙素基因相关肽(CGRP)与脑实质血管的调节

Calcitonin gene-related peptide (CGRP) and the regulation of cerebral parenchymal vessels.

作者信息

Kobari M, Fukuuchi Y, Tomita M, Tanahashi N, Takeda H, Yokoyama M

机构信息

Department of Neurology, School of Medicine, Keio University, Tokyo, Japan.

出版信息

Brain Res. 1995 Nov 6;698(1-2):95-9. doi: 10.1016/0006-8993(95)00833-c.

Abstract

The role of calcitonin gene-related peptide (CGRP) in the cerebral microcirculation was examined in fourteen anesthetized cats. The local cerebral blood volume (CBV) and blood flow (CBF) in the temporoparietal cortex were measured by our photoelectric method. CBV represents the cumulative dimensions of the parenchymal vascular network. Intracarotid injection of 0.1, 1, and 10 micrograms/kg CGRP8-37, a CGRP antagonist, had no significant effects on CBV and mean arterial blood pressure (MABP). Intracarotid injection of 0.1 and 1 microgram/kg CGRP, but not 0.01 microgram/kg CGRP, increased CBV in a dose-dependent manner (P < 0.05). CBV was initially reduced following 1 microgram/kg CGRP injection, possibly reflecting the marked fall in MABP (P < 0.01) with this dose. Following injection of 0.1 and 1 microgram/kg CGRP, CBF was also increased by +7.3 +/- 7.7 (+10.7%) and +13.1 +/- 4.8 ml/100 g brain/min (+20.4%, P < 0.05) at 15 min. The CBV increase elicited by 1 micrograms/kg CGRP was inhibited (P < 0.05) by preinjection of 10 micrograms/kg CGRP8-37. It is concluded that CGRP has no significant role in the maintenance of resting tone of intracerebral microvessels. However, circulating CGRP dilates the small parenchymal vessels through a specific CGRP receptor, and thereby is involved in the evolution of pathologic conditions.

摘要

在14只麻醉猫身上研究了降钙素基因相关肽(CGRP)在脑微循环中的作用。采用我们的光电方法测量颞顶叶皮质的局部脑血容量(CBV)和血流(CBF)。CBV代表实质血管网络的累积尺寸。颈内注射0.1、1和10微克/千克的CGRP拮抗剂CGRP8 - 37,对CBV和平均动脉血压(MABP)无显著影响。颈内注射0.1和1微克/千克的CGRP,但不包括0.01微克/千克的CGRP,以剂量依赖方式增加CBV(P < 0.05)。注射1微克/千克CGRP后,CBV最初降低,这可能反映了该剂量下MABP的显著下降(P < 0.01)。注射0.1和1微克/千克CGRP后,15分钟时CBF也分别增加了+7.3±7.7(+10.7%)和+13.1±4.8毫升/100克脑/分钟(+20.4%,P < 0.05)。预先注射10微克/千克的CGRP8 - 37可抑制1微克/千克CGRP引起的CBV增加(P < 0.05)。结论是,CGRP在维持脑微血管的静息张力方面无显著作用。然而,循环中的CGRP通过特定的CGRP受体使实质小血管扩张,从而参与病理状况的演变。

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