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Central B2 receptor involvement in the antinociceptive effect of bradykinin in rats.

机译:中枢B2受体参与了缓激肽在大鼠中的镇痛作用。

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摘要

1. The effect of intracerebroventricular (i.c.v.) injection of bradykinin (BK) and related peptides was tested on the dental pulp electrical stimulation threshold (DPEST) in rats. 2. BK (4, 8 and 16 nmol) induced a dose-dependent increase of DPEST, indicative of an antinociceptive effect. 3. I.c.v. injection of equimolar doses of BK-related peptides, Lys-BK and Met-Lys-BK, also induced an increase of DPEST, but the magnitude of the effect was not as intensive as that induced by BK, when the maximum increase of DPEST was considered. The peptide T-kinin induced a short lasting and weak antinociceptive effect. 4. The B1 agonist, des-Arg9-BK (8 nmol) induced a significant antinociceptive effect, but this was not as intensive as that induced by BK. 5. The B2 antagonist D-Arg0-Hyp3-Thi5,8-D-Phe7-BK (D-Arg0) competitively antagonized the BK-induced antinociception. Likewise, Hyp3-Thi5,8-D-Phe7-BK (Hyp) also antagonized BK effect. However, the compound Thi5,8-D-Phe7-BK (Thi), initially considered a pure BK antagonist, induced an antinociceptive effect, supporting previous observations that this peptide can also act as a partial agonist. 6. It is concluded that the dose-dependent antinociceptive effect induced by i.c.v. injection of BK is mediated by the stimulation of brain B2 receptors.
机译:1.在大鼠的牙髓电刺激阈值(DPEST)上测试了脑室内(i.c.v.)注射缓激肽(BK)和相关肽的作用。 2. BK(4、8和16 nmol)引起DPEST剂量依赖性增加,表明其具有镇痛作用。 3. I.c.v.注射等摩尔剂量的BK相关肽Lys-BK和Met-Lys-BK也会引起DPEST增加,但是当DPEST的最大增加为考虑过的。肽T激肽诱导了短暂且弱的抗伤害感受作用。 4. B1激动剂des-Arg9-BK(8 nmol)诱导了显着的抗伤害作用,但强度不如BK强烈。 5. B2拮抗剂D-Arg0-Hyp3-Thi5,8-D-Phe7-BK(D-Arg0)竞争性拮抗BK诱导的抗伤害感受。同样,Hyp3-Thi5,8-D-Phe7-BK(Hyp)也拮抗BK效应。然而,最初被认为是纯BK拮抗剂的化合物Thi5,8-D-Phe7-BK(Thi)诱导了抗伤害感受作用,支持了以前的观点,即该肽还可以作为部分激动剂。 6.结论是i.c.v.诱导的剂量依赖性抗伤害感受作用。 BK的注射是由脑B2受体的刺激介导的。

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