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CI988, a selective antagonist of cholecystokininB receptors, prevents morphine tolerance in the rat.CI988,一种胆囊收缩素B受体的选择性拮抗剂,可预防大鼠的吗啡耐受性。
Br J Pharmacol. 1992 Mar;105(3):591-6. doi: 10.1111/j.1476-5381.1992.tb09024.x.
2
The selective CCK-B receptor antagonist L-365,260 enhances morphine analgesia and prevents morphine tolerance in the rat.
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3
The CCK-B antagonist CI988 enhances the reflex-depressive effect of morphine in axotomized rats.胆囊收缩素B受体拮抗剂CI988增强吗啡对轴突切断大鼠的反射抑制作用。
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The CCK-B receptor antagonist Cl 988 reverses tolerance to morphine in rats.胆囊收缩素B受体拮抗剂氯988可逆转大鼠对吗啡的耐受性。
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Inhibition of morphine withdrawal by the association of RB 101, an inhibitor of enkephalin catabolism, and the CCKB antagonist PD-134,308.脑啡肽分解代谢抑制剂RB 101与CCKB拮抗剂PD-134,308联合使用对吗啡戒断的抑制作用。
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Dissociation of tolerance and dependence to morphine: a possible role for cholecystokinin.吗啡耐受性与依赖性的分离:胆囊收缩素的潜在作用
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7
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8
PD134308, a selective antagonist of cholecystokinin type B receptor, enhances the analgesic effect of morphine and synergistically interacts with intrathecal galanin to depress spinal nociceptive reflexes.PD134308,一种胆囊收缩素B型受体的选择性拮抗剂,可增强吗啡的镇痛效果,并与鞘内注射甘丙肽协同作用以抑制脊髓伤害性反射。
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The antagonism of benzodiazepine withdrawal effects by the selective cholecystokininB receptor antagonist CI-988.选择性胆囊收缩素B受体拮抗剂CI-988对苯二氮䓬戒断效应的拮抗作用。
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The selective cholecystokininB receptor antagonist L-365,260 diminishes the expression of naloxone-induced morphine withdrawal symptoms in normal and neuropathic rats.选择性胆囊收缩素B受体拮抗剂L-365,260可减轻正常大鼠和神经病理性大鼠中纳洛酮诱发的吗啡戒断症状的表达。
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Chronic morphine treatment modulates the extracellular levels of endogenous enkephalins in rat brain structures involved in opiate dependence: a microdialysis study.慢性吗啡治疗对参与阿片类药物依赖的大鼠脑结构中内源性脑啡肽的细胞外水平有调节作用:一项微透析研究。
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A locus and mechanism of action for associative morphine tolerance.联合吗啡耐受性的一个基因座及作用机制。
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Analgesic tolerance produced by morphine pellets is facilitated by analgesic testing.
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Prior hot plate exposure enhances morphine analgesia in tolerant and drug-naive rats.先前的热板暴露增强了耐受大鼠和未接触过药物大鼠的吗啡镇痛作用。
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Nociceptive assessment modifies behavioral tolerance without altering brain morphine concentration.伤害性评估可改变行为耐受性,而不改变脑内吗啡浓度。
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Separation of morphine analgesia from physical dependence.吗啡镇痛作用与身体依赖性的分离。
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Proglumide prevents and curtails acute tolerance to morphine in rats.丙谷胺可预防和减轻大鼠对吗啡的急性耐受性。
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Evidence for the neuropeptide cholecystokinin as an antagonist of opiate analgesia.神经肽缩胆囊素作为阿片类镇痛拮抗剂的证据。
Science. 1983 Jan 21;219(4582):310-2. doi: 10.1126/science.6294831.
8
Caerulein and cholecystokinin suppress beta-endorphin-induced analgesia in the rat.蛙皮素和胆囊收缩素可抑制大鼠体内β-内啡肽诱导的镇痛作用。
Eur J Pharmacol. 1982 Jun 4;80(4):421-5. doi: 10.1016/0014-2999(82)90089-9.
9
Distinct cholecystokinin receptors in brain and pancreas.大脑和胰腺中不同的胆囊收缩素受体。
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Cholecystokinin receptors in the brain: characterization and distribution.大脑中的胆囊收缩素受体:特性与分布
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CI988,一种胆囊收缩素B受体的选择性拮抗剂,可预防大鼠的吗啡耐受性。

CI988, a selective antagonist of cholecystokininB receptors, prevents morphine tolerance in the rat.

作者信息

Xu X J, Wiesenfeld-Hallin Z, Hughes J, Horwell D C, Hökfelt T

机构信息

Department of Clinical Physiology, Karolinska Institute, Huddinge University Hospital, Sweden.

出版信息

Br J Pharmacol. 1992 Mar;105(3):591-6. doi: 10.1111/j.1476-5381.1992.tb09024.x.

DOI:10.1111/j.1476-5381.1992.tb09024.x
PMID:1628146
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1908430/
Abstract
  1. The effect of chronic treatment with CI988, a recently developed selective antagonist of cholecystokinin type-B receptors (CCKB receptors) on the tolerance to morphine analgesia was studied in rats with the hot plate test. 2. Morphine tolerance was induced with the use of two paradigms. Morphine was injected i.p. either in a schedule of increasing doses (1-32 mg kg-1) twice daily for 6 days or at a fixed dose (3 mg kg-1) daily for 29 days. 3. In both series of experiments, tolerance to the analgesic effect of morphine was prevented by simultaneous treatment with i.p. CI988. Chronic treatment with only CI988 daily for up to 29 days did not reduce the analgesic effect of a weekly injection of morphine. 4. CI988 did not diminish the physical dependence to morphine, as examined with naloxone precipitated withdrawal. 5. The present results provide evidence that chronic treatment with a selective CCKB receptor antagonist could prevent tolerance to the analgesic effect of morphine without affecting morphine-induced physical dependence. Application of CCK antagonists may be clinically important in treating chronic pain patients by preventing morphine tolerance and by eliminating the need to increase morphine doses to unacceptable levels.
摘要
  1. 采用热板试验,研究了最近开发的胆囊收缩素B型受体(CCKB受体)选择性拮抗剂CI988长期治疗对大鼠吗啡镇痛耐受性的影响。2. 采用两种方案诱导吗啡耐受性。吗啡腹腔注射,一种方案是每日两次递增剂量(1 - 32毫克/千克),持续6天;另一种方案是每日固定剂量(3毫克/千克),持续29天。3. 在这两个系列实验中,腹腔注射CI988同时给药可预防对吗啡镇痛作用的耐受性。仅每日用CI988长期治疗长达29天,并不降低每周一次注射吗啡的镇痛效果。4. 用纳洛酮诱发戒断反应检测发现,CI988并不减弱对吗啡的身体依赖性。5. 目前的结果表明,用选择性CCKB受体拮抗剂长期治疗可预防对吗啡镇痛作用的耐受性,而不影响吗啡诱导的身体依赖性。CCK拮抗剂的应用在治疗慢性疼痛患者方面可能具有临床重要性,可预防吗啡耐受性,并避免将吗啡剂量增加到不可接受的水平。