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阿片类激动剂-拮抗剂对小鼠吗啡诱导的过度兴奋和镇痛的不同作用。

Differential effects of opiate agonists-antagonists on morphine-induced hyperexcitability and analgesia in mice.

作者信息

Filibeck U, Castellano C, Oliverio A

出版信息

Psychopharmacology (Berl). 1981;73(2):134-6. doi: 10.1007/BF00429203.

DOI:10.1007/BF00429203
PMID:6785803
Abstract

The effects of two opiate agonists-antagonists, butorphanol (4.0 and 8.0 mg/kg) and buprenorphine (0.1 and 1.0 mg/kg), were assessed on locomotor activity and analgesia in DBA/2 and C57BL/6 mice. Different behavioral effects were evident in these strains, which might be characterized by different reactions to the effects of opiates and by differences in endorphin distributions and opiate receptor populations. In particular, buprenorphine acted as an agonist-antagonist to morphine in both strains while a dissociation of butorphanol effects was evident, depending on the strain considered. The clinical implications of these findings are discussed.

摘要

评估了两种阿片类激动剂 - 拮抗剂布托啡诺(4.0 和 8.0 毫克/千克)和丁丙诺啡(0.1 和 1.0 毫克/千克)对 DBA/2 和 C57BL/6 小鼠运动活性和镇痛作用的影响。在这些品系中观察到了不同的行为效应,这可能表现为对阿片类药物作用的不同反应以及内啡肽分布和阿片受体数量的差异。特别是,丁丙诺啡在两种品系中对吗啡均表现为激动 - 拮抗剂作用,而布托啡诺的效应则明显不同,这取决于所考虑的品系。讨论了这些发现的临床意义。

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1
Differential effects of opiate agonists-antagonists on morphine-induced hyperexcitability and analgesia in mice.阿片类激动剂-拮抗剂对小鼠吗啡诱导的过度兴奋和镇痛的不同作用。
Psychopharmacology (Berl). 1981;73(2):134-6. doi: 10.1007/BF00429203.
2
[Effect of agonistic morphine antagonists (cyclazocine, butorphanol, buprenorphine) on EEG activity and the depth of anesthesia in rats].[激动性吗啡拮抗剂(环唑辛、布托啡诺、丁丙诺啡)对大鼠脑电图活动及麻醉深度的影响]
Masui. 1987 Apr;36(4):490-7.
3
Physical dependence induced by opiate partial agonists in the rat.阿片类部分激动剂在大鼠中诱导的身体依赖性。
Neuropeptides. 1984 Dec;5(1-3):11-4. doi: 10.1016/0143-4179(84)90014-3.
4
In vivo receptor binding of the opiate partial agonist, buprenorphine, correlated with its agonistic and antagonistic actions.阿片类部分激动剂丁丙诺啡的体内受体结合与其激动和拮抗作用相关。
Br J Pharmacol. 1981 Nov;74(3):627-33. doi: 10.1111/j.1476-5381.1981.tb10473.x.
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Agonist action of the agonist/antagonist analgesic butorphanol on dopamine metabolism in the nucleus accumbens of the rat.激动剂/拮抗剂镇痛药布托啡诺对大鼠伏隔核多巴胺代谢的激动作用。
Neurosci Lett. 1987 Jun 15;77(2):226-30. doi: 10.1016/0304-3940(87)90591-x.
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Review of self-administration.自我给药的综述。
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[Effect of butorphanol and buprenorphine on cerebrospinal fluid pressure].[布托啡诺和丁丙诺啡对脑脊液压力的影响]
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[Interactions between buprenorphine, narcotic analgesic, and centrally acting drugs in prolongation of halothane-induced sleeping and analgesia (author's transl)].丁丙诺啡、麻醉性镇痛药与中枢作用药物之间在延长氟烷诱导的睡眠和镇痛方面的相互作用(作者译)
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Effects of butorphanol, flunixin, levorphanol, morphine, and xylazine in ponies.布托啡诺、氟尼辛、左啡诺、吗啡和赛拉嗪对小马的影响。
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Effect of Morphine and butorphanol on gallbladder emptying.
Can J Surg. 1983 Jan;26(1):70-1.

引用本文的文献

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Role of efficacy as a determinant of locomotor activation by mu-opioid receptor (MOR) ligands in female and male mice. II. Effects of novel MOR-selective phenylmorphans with high-to-low MOR efficacy.阿片受体(MOR)配体对雌性和雄性小鼠运动激活作用的功效决定作用。二、高至低 MOR 功效的新型 MOR 选择性苯吗喃的影响。
Pharmacol Res Perspect. 2023 Aug;11(4):e01111. doi: 10.1002/prp2.1111.
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Thermal latency studies in opiate-treated mice.阿片类药物处理小鼠的热潜伏期研究。
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The effects of chronic buprenorphine on intake of heroin and cocaine in rats and its effects on nucleus accumbens dopamine levels during self-administration.

本文引用的文献

1
Buprenorphine suppresses heroin use by heroin addicts.丁丙诺啡可抑制海洛因成瘾者对海洛因的使用。
Science. 1980 Feb 8;207(4431):657-9. doi: 10.1126/science.7352279.
2
Genotype-dependent sensitivity to morphine: role of different opiate receptor populations.基因型对吗啡的敏感性:不同阿片受体群体的作用
Brain Res. 1980 May 5;189(1):289-94. doi: 10.1016/0006-8993(80)90031-1.
3
Requirements for extinction of relapse-facilitating variables and for rehabilitation in a narcotic-antagonist treatment program.在麻醉拮抗剂治疗方案中,消除促进复发变量及康复的要求。
慢性丁丙诺啡对大鼠海洛因和可卡因摄入量的影响及其在自我给药过程中对伏隔核多巴胺水平的影响。
Psychopharmacology (Berl). 2006 Sep;188(1):28-41. doi: 10.1007/s00213-006-0485-1. Epub 2006 Aug 11.
4
Tripelennamine enhances buprenorphine-, but not pentazocine-induced hyperactivity in mice.曲吡那敏增强小鼠中丁丙诺啡诱导的多动,但不增强喷他佐辛诱导的多动。
Psychopharmacology (Berl). 1988;95(2):176-9. doi: 10.1007/BF00174505.
5
Opioids and behavior: genetic aspects.阿片类药物与行为:遗传学方面
Experientia. 1988 Jun 15;44(6):473-81. doi: 10.1007/BF01958921.
6
Inbred strain differences in morphine-induced analgesia with the hot plate assay: a reassessment.采用热板法对吗啡诱导镇痛的近交系差异进行的重新评估。
Behav Genet. 1990 Mar;20(2):333-8. doi: 10.1007/BF01067800.
Adv Biochem Psychopharmacol. 1973;8(0):399-414.
4
Genotype-dependent sensitivity and tolerance to morphine and heroin: dissociation between opiate-induced running and analgesia in the mouse.基因型依赖性对吗啡和海洛因的敏感性与耐受性:小鼠中阿片类药物诱导的奔跑行为与镇痛作用的分离
Psychopharmacologia. 1974;39(1):13-22. doi: 10.1007/BF00421454.
5
Mixed agonist-antagonist opiates and physical dependence.混合激动剂-拮抗剂阿片类药物与身体依赖性
Br J Clin Pharmacol. 1979;7 Suppl 3(Suppl 3):291S-296S. doi: 10.1111/j.1365-2125.1979.tb04703.x.
6
Differential effects of localized lesions of n. accumbens on morphine- and amphetamine-induced locomotor hyperactivity in the C57BL/6J mouse.伏隔核局部损伤对C57BL/6J小鼠吗啡和苯丙胺诱导的运动性活动亢进的不同影响。
J Comp Physiol Psychol. 1979 Aug;93(4):745-51. doi: 10.1037/h0077605.
7
The animal pharmacology of buprenorphine, an oripavine analgesic agent.丁丙诺啡(一种阿片类镇痛药)的动物药理学。
Br J Pharmacol. 1977 Aug;60(4):547-54. doi: 10.1111/j.1476-5381.1977.tb07533.x.
8
Agonist and antagonist properties of buprenorphine, a new antinociceptive agent.新型抗伤害感受剂丁丙诺啡的激动剂和拮抗剂特性
Br J Pharmacol. 1977 Aug;60(4):537-45. doi: 10.1111/j.1476-5381.1977.tb07532.x.
9
History and development of mixed opioid agonists, partial agonists and antagonists.混合阿片类激动剂、部分激动剂和拮抗剂的历史与发展
Br J Clin Pharmacol. 1979;7 Suppl 3(Suppl 3):273S-279S. doi: 10.1111/j.1365-2125.1979.tb04700.x.
10
Analgesic effectiveness of the narcotic agonist-antagonists.麻醉性激动剂-拮抗剂的镇痛效果。
Br J Clin Pharmacol. 1979;7 Suppl 3(Suppl 3):297S-308S. doi: 10.1111/j.1365-2125.1979.tb04704.x.