首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >Effects of the delta-opioid receptor antagonist naltrindole on antinociceptive responses to selective delta-agonists in post-weanling rats.
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Effects of the delta-opioid receptor antagonist naltrindole on antinociceptive responses to selective delta-agonists in post-weanling rats.

机译:阿片类鸦片受体拮抗剂纳曲酮对断奶后大鼠选择性δ-激动剂抗伤害感受反应的影响。

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摘要

1. Antagonism, by the selective delta-opioid receptor antagonist naltrindole, of the antinociceptive effects of [D-Pen2, D-Pen5] enkephalin (DPDPE), [D-Ser2, Leu5, Thr6] enkephalin (DSLET) and D-Ala2 deltorphin I (DELT I) has been studied in 25 day old rats. 2. Antinociception was measured by the 50 degrees C tail immersion test following i.p. administration of agonists and/or antagonists. 3. Dose-related antinociception was observed with DPDPE, DSLET and DELT I and ED75 doses were computed (0.66 mg kg-1, 0.65 mg kg-1, 0.032 mg kg-1 respectively) and used for antagonism studies. 4. Naltrindole (0.01 mg kg-1) significantly attenuated the antinociceptive effects of DPDPE and DSLET with 0.1 mg kg-1 producing complete reversal of the effects of the ED75 dose. In contrast, naltrindole at 0.01 and 0.1 mg kg-1 did not alter antinociceptive responses to DELT I. Naltrindole at 1 mg kg-1 significantly attenuated DELT I antinociception. 5. Naloxone (1 mg kg-1) produced equivalent degrees of antagonism of the antinociceptive effects of DPDPE, DSLET and DELT I. ICI 174,864 (1 mg kg-1) also antagonized antinociception with a differential degree of attenuation (DSLET > DPDPE > DELT I). 6. Naltrindole (1 mg kg-1) had no effect on the antinociception induced by the selective mu-agonist alfentanil (60 micrograms kg-1). Naltrindole, naloxone or ICI 174,864 had no effect on nociceptive latencies. 7. The differential antagonism by naltrindole of the effects of three selective delta-agonists suggests delta-receptor heterogeneity.(ABSTRACT TRUNCATED AT 250 WORDS)
机译:1.通过选择性δ-阿片受体拮抗剂纳曲酮对[D-Pen2,D-Pen5]脑啡肽(DPDPE),[D-Ser2,Leu5,Thr6]脑啡肽(DSLET)和D-Ala2的抗伤害作用已在25日龄大鼠中研究了deltorphin I(DELT I)。 2.在腹腔注射后,通过50℃的尾部浸没试验来测量抗伤害感受。激动剂和/或拮抗剂的给药。 3.用DPDPE观察到剂量相关的抗伤害感受,计算了DSLET和DELT I的剂量,并计算了ED75的剂量(分别为0.66 mg kg-1、0.65 mg kg-1、0.032 mg kg-1),并用于拮抗作用研究。 4.纳曲酮(0.01 mg kg-1)显着减弱了DPDPE和DSLET的抗伤害感受性,而0.1 mg kg-1则完全逆转了ED75剂量的作用。相比之下,在0.01和0.1 mg kg-1的纳曲酮没有改变对DELT I的镇痛反应。在1 mg kg-1的纳曲酮显着减弱了DELT I的镇痛作用。 5.纳洛酮(1 mg kg-1)与DPDPE,DSLET和DELT I具有相同程度的拮抗作用。ICI 174,864(1 mg kg-1)也具有不同程度的减弱作用(DSLET> DPDPE> DELT I)。 6.纳曲酮(1mg kg-1)对选择性μ-激动剂阿芬太尼(60μgkg-1)诱导的抗伤害感受没有作用。纳曲酮,纳洛酮或ICI 174864对伤害性潜伏期没有影响。 7.纳曲酮对三种选择性δ-激动剂的不同拮抗作用表明δ-受体异质性。(摘要截短为250字)

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