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本文引用的文献

1
Dose response relationships during perinatal lead administration in the rat: a model for the study of lead effects on brain development.大鼠围产期铅给药期间的剂量反应关系:铅对脑发育影响研究的一个模型
Toxicology. 1981;21(2):117-28. doi: 10.1016/0300-483x(81)90122-0.
2
Dose-dependent and reversible effects of lead on rat dopaminergic system.
Life Sci. 1981 Feb 16;28(7):795-9. doi: 10.1016/0024-3205(81)90163-6.
3
Low-level lead exposure alters morphine antinociception in neonatal rats.低水平铅暴露会改变新生大鼠对吗啡的镇痛反应。
Toxicol Lett. 1984 Aug;22(2):119-23. doi: 10.1016/0378-4274(84)90054-7.
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Stress and endogenous opioid peptides: a review.压力与内源性阿片肽:综述
Mod Probl Pharmacopsychiatry. 1981;17:49-67. doi: 10.1159/000402406.
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Brain neurotransmitter system and chronic lead intoxication.脑神经递质系统与慢性铅中毒。
Pharmacol Res Commun. 1980 May;12(5):447-60. doi: 10.1016/s0031-6989(80)80115-9.
6
Ontogenesis of proenkephalin products in rat striatum and the inhibitory effects of low-level lead exposure.大鼠纹状体中前脑啡肽原产物的个体发生及低水平铅暴露的抑制作用。
Brain Res. 1985 Sep;354(1):75-9. doi: 10.1016/0165-3806(85)90070-7.
7
Ontogeny of catecholamine and GABA levels in rat brain: lack of effect of perinatal lead exposure.大鼠脑中儿茶酚胺和γ-氨基丁酸水平的个体发生:围产期铅暴露无影响。
Toxicol Lett. 1986 Jan;30(1):97-102. doi: 10.1016/0378-4274(86)90184-0.
8
Two types of chronic lead treatment in C57BL/6 mice: interaction with behavioural determinants of pain.C57BL/6小鼠的两种慢性铅治疗方式:与疼痛行为决定因素的相互作用
Life Sci. 1986 Jul 7;39(1):47-53. doi: 10.1016/0024-3205(86)90436-4.
9
Opioid and non-opioid stress analgesia from cold water swim: importance of stress severity.冷水游泳产生的阿片类和非阿片类应激镇痛:应激严重程度的重要性。
Brain Res. 1986 Apr 30;372(1):167-71. doi: 10.1016/0006-8993(86)91472-1.
10
Impairment of ketocyclazocine antinociception in rats by perinatal lead exposure.围产期铅暴露对大鼠酮环佐辛镇痛作用的损害。
Toxicol Lett. 1985 Aug;26(2-3):101-5. doi: 10.1016/0378-4274(85)90152-3.

围产期铅暴露会损害发育中大鼠的阿片类药物介导而非非阿片类药物介导的应激诱导的抗伤害感受。

Perinatal lead exposure impairs opioid but not non-opioid stress-induced antinociception in developing rats.

作者信息

Jackson H C, Kitchen I

机构信息

Department of Biochemistry, University of Surrey, Guildford.

出版信息

Br J Pharmacol. 1989 Aug;97(4):1338-42. doi: 10.1111/j.1476-5381.1989.tb12597.x.

DOI:10.1111/j.1476-5381.1989.tb12597.x
PMID:2551447
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1854625/
Abstract
  1. The development of opioid systems has been shown to be sensitive to perinatal exposure to lead. We have studied the effects of such exposure on opioid and non-opioid mediated stress-induced antinociception in developing rats. 2. Lead was administered in the maternal drinking water from conception to postnatal day 14 at 300 and 1000 p.p.m. Twenty and 25 day old rats were subjected to swimming stress and antinociception measured using the tail immersion test. 3. A 3 min swim-stress induced an opioid-mediated antinociceptive response in 20 day old rats which was attenuated by 300 p.p.m. lead and by 1000 p.p.m. lead treatment in a dose-related manner. A 10 min swim-stress induced a non-opioid mediated antinociceptive response in 25 day old rats which was not antagonised by 300 or 1000 p.p.m. lead. 4. Naloxone antagonised the residual antinociception observed in 20 day old animals treated with 300 p.p.m. lead and had no effect on antinociception in control or lead-treated 25 day old rats. 5. Using a lead exposure model considered to represent subclinical lead toxicity in man, it was shown that perinatal lead exposure disrupts opioid but not non-opioid mediated stress antinociception.
摘要
  1. 已表明阿片系统的发育对围产期铅暴露敏感。我们研究了这种暴露对发育中大鼠阿片类和非阿片类介导的应激诱导的抗伤害感受的影响。2. 从受孕到出生后第14天,以300和1000 ppm的浓度将铅添加到母鼠饮用水中。对20日龄和25日龄的大鼠施加游泳应激,并使用尾浸试验测量抗伤害感受。3. 3分钟的游泳应激在20日龄大鼠中诱导出阿片类介导的抗伤害感受反应,该反应在300 ppm铅和1000 ppm铅处理下以剂量相关的方式减弱。10分钟的游泳应激在25日龄大鼠中诱导出非阿片类介导的抗伤害感受反应,该反应未被300或1000 ppm铅拮抗。4. 纳洛酮拮抗了在接受300 ppm铅处理的20日龄动物中观察到的残余抗伤害感受,对对照或铅处理的25日龄大鼠的抗伤害感受没有影响。5. 使用被认为代表人类亚临床铅毒性的铅暴露模型,结果表明围产期铅暴露会破坏阿片类介导的应激抗伤害感受,但不会破坏非阿片类介导的应激抗伤害感受。