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M1毒蕈碱受体阻断对大鼠创伤性脑损伤后行为和生理反应的影响。

The effect of M1 muscarinic blockade on behavior and physiological responses following traumatic brain injury in the rat.

作者信息

Robinson S E, Foxx S D, Posner M G, Martin R M, Davis T R, Guo H Z, Enters E K

机构信息

Department of Pharmacology and Toxicology, Medical College of Virginia, Virginia Commonwealth University, Richmond 23298-0613.

出版信息

Brain Res. 1990 Mar 12;511(1):141-8. doi: 10.1016/0006-8993(90)90233-2.

DOI:10.1016/0006-8993(90)90233-2
PMID:2331611
Abstract

Dicyclomine (1 mg/kg or 10 mg/kg), scopolamine (1 mg/kg), or saline was administered intraperitoneally to rats 15 min prior to moderate fluid percussion brain injury. A variety of reflexes and responses were measured up to 60 min following injury, and body weight and several neurological measures were taken daily up to 10 days following injury. All 3 antimuscarinic treatments reduced the duration of transient behavioral suppression as assessed by these measures. It appears that blockade of the M1 muscarinic receptor can attenuate transient behavioral suppression associated with concussive brain injury. Thus, stimulation of M1 muscarinic receptors may mediate components of reversible traumatic unconsciousness following cerebral concussion. No differences were observed between saline and antimuscarinic treatments in the incidence or duration of apnea following injury. Scopolamine pretreatment significantly elevated heart rate prior to injury, but had no significant effect on the responses of heart rate and blood pressure to experimental concussion. Both doses of dicyclomine significantly reduced resting heart rate, but unlike scopolamine, significantly enhanced the cardiovascular response to fluid percussion injury. Antimuscarinic treatment significantly reduced body weight loss and certain motor deficits, including beam balance and beam walk performance, following concussive head injury. Scopolamine and both doses of dicyclomine appeared to be equally effective in reducing long-term deficits. Data from these experiments indicate that at least some of the long-term behavioral deficits following moderate levels of brain injury may involve the binding of acetylcholine to M1 muscarinic receptors.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在对大鼠进行中度液体冲击性脑损伤前15分钟,腹腔注射双环维林(1毫克/千克或10毫克/千克)、东莨菪碱(1毫克/千克)或生理盐水。在损伤后的60分钟内测量多种反射和反应,并在损伤后的10天内每天测量体重和多项神经学指标。通过这些指标评估发现,所有三种抗毒蕈碱治疗均缩短了短暂行为抑制的持续时间。似乎M1毒蕈碱受体的阻断可减轻与脑震荡相关的短暂行为抑制。因此,M1毒蕈碱受体的刺激可能介导脑震荡后可逆性创伤性昏迷的某些成分。在损伤后呼吸暂停的发生率或持续时间方面,生理盐水和抗毒蕈碱治疗之间未观察到差异。东莨菪碱预处理在损伤前显著提高了心率,但对心率和血压对实验性脑震荡的反应没有显著影响。两种剂量的双环维林均显著降低静息心率,但与东莨菪碱不同的是,它显著增强了对液体冲击性损伤的心血管反应。抗毒蕈碱治疗显著减少了脑震荡性头部损伤后的体重减轻和某些运动缺陷,包括横梁平衡和横梁行走表现。东莨菪碱和两种剂量的双环维林在减少长期缺陷方面似乎同样有效。这些实验的数据表明,中度脑损伤后的至少一些长期行为缺陷可能涉及乙酰胆碱与M1毒蕈碱受体的结合。(摘要截断于250字)

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The effect of M1 muscarinic blockade on behavior and physiological responses following traumatic brain injury in the rat.M1毒蕈碱受体阻断对大鼠创伤性脑损伤后行为和生理反应的影响。
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Dicyclomine, an M1 muscarinic antagonist, reduces biomarker levels, but not neuronal degeneration, in fluid percussion brain injury.双环胺,一种M1毒蕈碱拮抗剂,可降低液体冲击脑损伤中的生物标志物水平,但不能减少神经元变性。
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