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Pharmacological characterization of the cardiovascular responses elicited by kinin B(1) and B(2) receptor agonists in the spinal cord of streptozotocin-diabetic rats.链脲佐菌素诱导的糖尿病大鼠脊髓中激肽B(1)和B(2)受体激动剂引起的心血管反应的药理学特征
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The effect of long-term streptozotocin-induced diabetes on contractile and relaxation responses of coronary arteries: selective attenuation of CGRP-induced relaxations.长期链脲佐菌素诱导的糖尿病对冠状动脉收缩和舒张反应的影响:降钙素基因相关肽诱导舒张的选择性减弱。
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糖尿病大鼠的神经源性皮肤血管舒张和血浆外渗:胰岛素和神经生长因子的作用

Neurogenic cutaneous vasodilatation and plasma extravasation in diabetic rats: effect of insulin and nerve growth factor.

作者信息

Bennett G S, Garrett N E, Diemel L T, Brain S D, Tomlinson D R

机构信息

Pharmacology Group and Vascular Biology Research Centre, King's College, London.

出版信息

Br J Pharmacol. 1998 Aug;124(7):1573-9. doi: 10.1038/sj.bjp.0701986.

DOI:10.1038/sj.bjp.0701986
PMID:9723973
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1565543/
Abstract
  1. Neurogenic vasoactive responses in rat skin were investigated following 8 weeks of streptozotocin-induced diabetes to determine the effect of diabetes and of treatment with insulin and nerve growth factor (NGF) treatment. 2. Diabetic rats were divided into three groups: untreated; insulin (4 IU day(-1) by s.c. implant weeks 4-8) treated; Nerve Growth Factor, NGF, (0.2 mg kg(-1) three times weekly, weeks 4-8) treated. A fourth group served as a non-diabetic control. 3. Electrical stimulation of the saphenous nerve (10 V, 2 Hz, 1 ms for 30 s) increased blood flow in the ipsilateral paw skin, as measured by laser Doppler flowmetry. The peak increase was similar between groups, but the time taken for flow to return to a steady baseline was significantly (P < 0.01) reduced in untreated diabetic rats, when compared with non-diabetic controls, but not significantly reduced in the insulin- or NGF-treated diabetic groups. 4. A second stimulation of the saphenous nerve (10 V, 2 Hz, 1 ms for 5 min) produced plasma extravasation, measured by the extravascular accumulation of 125I-albumin, in the skin. Plasma extravasation was significantly attenuated (P < 0.001) in the untreated diabetic group, but not the insulin-treated group, compared to non-diabetic controls. Plasma extravasation was present, though reduced, in the NGF-treated group. 5. Plasma extravasation induced by intradermal injections of substance P with and without CGRP was similar in all groups indicating no decrease in vascular responsiveness to exogenously applied neuropeptides. The results suggest that release of neuropeptides is diminished in diabetes and that treatment with either insulin or NGF can restore neurogenic microvascular vasoactive responses towards normal.
摘要
  1. 在链脲佐菌素诱导的糖尿病大鼠持续8周后,研究其皮肤中的神经源性血管活性反应,以确定糖尿病以及胰岛素和神经生长因子(NGF)治疗的效果。2. 糖尿病大鼠分为三组:未治疗组;胰岛素治疗组(第4 - 8周皮下植入,每天4 IU);神经生长因子(NGF)治疗组(第4 - 8周,每周三次,每次0.2 mg/kg)。第四组作为非糖尿病对照组。3. 通过激光多普勒血流仪测量,电刺激隐神经(10 V,2 Hz,1 ms,持续30 s)可增加同侧爪皮肤的血流量。各组的峰值增加相似,但与非糖尿病对照组相比,未治疗的糖尿病大鼠血流恢复到稳定基线所需的时间显著缩短(P < 0.01),而胰岛素或NGF治疗的糖尿病组则无显著缩短。4. 再次刺激隐神经(10 V,2 Hz,1 ms,持续5 min)会导致皮肤出现血浆外渗,通过125I - 白蛋白的血管外积聚来测量。与非糖尿病对照组相比,未治疗的糖尿病组血浆外渗显著减弱(P < 0.001),而胰岛素治疗组则没有。NGF治疗组存在血浆外渗,尽管有所减少。5. 在所有组中,皮内注射P物质以及联合降钙素基因相关肽(CGRP)诱导的血浆外渗相似,表明对外源性应用的神经肽的血管反应性没有降低。结果表明,糖尿病中神经肽的释放减少,胰岛素或NGF治疗均可使神经源性微血管血管活性反应恢复正常。