• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

作为评估小鼠肌肉松弛手段的定量握力评估

Quantitative grip strength assessment as a means of evaluating muscle relaxation in mice.

作者信息

Nevins M E, Nash S A, Beardsley P M

机构信息

Department of Neurological Diseases Research, Searle, Skokie, IL 60077.

出版信息

Psychopharmacology (Berl). 1993;110(1-2):92-6. doi: 10.1007/BF02246955.

DOI:10.1007/BF02246955
PMID:7870904
Abstract

The effects of various centrally acting drugs and some peripherally acting agents on the forelimb grip strength of CD-1 mice were explored. Forelimb grip strength was assessed by use of a strain gauge to measure the lateral pull force, in grams, exerted by mice as an index of muscle relaxation. The muscle relaxants, diazepam, midazolam, baclofen, methocarbamol, dantrolene sodium and the neuromuscular blocking agents, succinylcholine and pancuronium bromide, dose-dependently reduced forelimb grip strength. 2-Amino-7-phosphonoheptanoic acid (AP7), which has also been shown to have muscle relaxant effects, also reduced grip strength. Pentobarbital, ethanol, phencyclidine, ketamine and chlorpromazine reduced grip strength at doses which produced behavioral impairments. Lithium chloride, a toxic compound used to induce taste aversions, and clonidine, at doses which affect blood pressure, body temperature and locomotor activity, did not affect grip strength. In addition, stimulant doses of amphetamine and caffeine, but not of morphine, increased grip strength in a dose-dependent manner. These results extend previous findings and suggest that this forelimb grip strength procedure may be a useful screening test for the identification of the potential muscle relaxant properties of drugs.

摘要

研究了各种中枢作用药物和一些外周作用药物对CD-1小鼠前肢握力的影响。使用应变仪测量小鼠施加的横向拉力(以克为单位)来评估前肢握力,以此作为肌肉松弛的指标。肌肉松弛剂地西泮、咪达唑仑、巴氯芬、美索巴莫、丹曲林钠以及神经肌肉阻滞剂琥珀酰胆碱和泮库溴铵,均剂量依赖性地降低前肢握力。2-氨基-7-膦酰庚酸(AP7)也已被证明具有肌肉松弛作用,它也降低了握力。戊巴比妥、乙醇、苯环己哌啶、氯胺酮和氯丙嗪在产生行为损伤的剂量下降低了握力。用于诱导味觉厌恶的有毒化合物氯化锂以及在影响血压、体温和运动活动的剂量下的可乐定,均未影响握力。此外,兴奋剂剂量的苯丙胺和咖啡因可剂量依赖性地增加握力,但吗啡则无此作用。这些结果扩展了先前的发现,并表明这种前肢握力测试方法可能是一种有用的筛选试验,用于鉴定药物潜在的肌肉松弛特性。

相似文献

1
Quantitative grip strength assessment as a means of evaluating muscle relaxation in mice.作为评估小鼠肌肉松弛手段的定量握力评估
Psychopharmacology (Berl). 1993;110(1-2):92-6. doi: 10.1007/BF02246955.
2
Influence of ethanol on the myorelaxant effect of diazepam in rats.乙醇对大鼠地西泮肌松作用的影响。
Acta Pharm. 2005 Mar;55(1):115-22.
3
Transdermal eperisone elicits more potent and longer-lasting muscle relaxation than oral eperisone.与口服乙哌立松相比,透皮乙哌立松能引起更有效且更持久的肌肉松弛。
Pharmacology. 2004 Jul;71(3):150-6. doi: 10.1159/000077449.
4
Comparative study in mice of tetrazepam and other centrally active skeletal muscle relaxants.替马西泮与其他中枢性骨骼肌松弛剂在小鼠体内的对比研究。
Arch Int Pharmacodyn Ther. 1989 Jan-Feb;297:272-85.
5
Factors affecting grip strength testing.影响握力测试的因素。
Neurotoxicol Teratol. 2003 Sep-Oct;25(5):543-53. doi: 10.1016/s0892-0362(03)00073-4.
6
A comparison of the neuromuscular blocking and autonomic effects of two new short-acting muscle relaxants with those of succinylcholine in the anesthetized cat and pig.
Anesthesiology. 1989 Mar;70(3):533-40. doi: 10.1097/00000542-198903000-00026.
7
Modified forelimb grip strength test detects aging-associated physiological decline in skeletal muscle function in male mice.改良后的前肢握力测试可检测雄性小鼠骨骼肌功能与衰老相关的生理衰退。
Sci Rep. 2017 Feb 8;7:42323. doi: 10.1038/srep42323.
8
Muscle relaxant activity of methocarbamol enantiomers in mice.美索巴莫对映体在小鼠体内的肌肉松弛活性。
J Pharm Pharmacol. 1999 Jul;51(7):853-5. doi: 10.1211/0022357991773069.
9
Characterization of acute adverse-effect profiles of selected antiepileptic drugs in the grip-strength test in mice.在小鼠握力试验中对选定抗癫痫药物的急性不良反应特征进行描述。
Pharmacol Rep. 2009 Jul-Aug;61(4):737-42. doi: 10.1016/s1734-1140(09)70128-8.
10
2-Amino-7-phosphonoheptanoic acid (AP7) produces discriminative stimuli and anticonflict effects similar to diazepam.2-氨基-7-膦酰庚酸(AP7)产生与地西泮相似的辨别性刺激和抗冲突效应。
Life Sci. 1986 Dec 22;39(25):2455-61. doi: 10.1016/0024-3205(86)90488-1.

引用本文的文献

1
Behavioral and Pharmacokinetics Studies of -Methyl-2-Aminoindane (NM2AI) in Mice: An Aminoindane Briefly Used in the Illicit Drug Market.-甲基-2-氨基茚满(NM2AI)在小鼠中的行为学和药代动力学研究:一种在非法毒品市场中短暂使用的氨基茚满。
Int J Mol Sci. 2023 Jan 18;24(3):1882. doi: 10.3390/ijms24031882.
2
Multi-Dose Intravenous Administration of Neutral and Cationic Liposomes in Mice: An Extensive Toxicity Study.小鼠中性和阳离子脂质体的多剂量静脉给药:一项广泛的毒性研究。
Pharmaceuticals (Basel). 2022 Jun 18;15(6):761. doi: 10.3390/ph15060761.
3
Carisoprodol Single and Multiple Dose PK-PD. Part II: Pharmacodynamics Evaluation Method for Central Muscle Relaxants. Double-Blind Placebo-Controlled Clinical Trial in Healthy Volunteers.

本文引用的文献

1
A note on a simple apparatus for detecting neurological deficit in rats and mice.关于一种用于检测大鼠和小鼠神经功能缺损的简易装置的说明。
J Am Pharm Assoc Am Pharm Assoc. 1957 Mar;46(3):208-9. doi: 10.1002/jps.3030460322.
2
A comparison of the rates of development of functional hexane neuropathy in weanling and young adult rats.断奶幼鼠和成年幼鼠功能性正己烷神经病变发展速率的比较。
Neurobehav Toxicol Teratol. 1983 Jan-Feb;5(1):63-8.
3
The hypothermic effect of clonidine and other imidazolidines in relation to their ability to enter the central nervous system in mice.
卡立普多单剂量与多剂量的药代动力学-药效学。第二部分:中枢性肌肉松弛剂的药效学评估方法。健康志愿者的双盲安慰剂对照临床试验。
J Clin Med. 2022 Feb 21;11(4):1141. doi: 10.3390/jcm11041141.
4
GABA Receptor Agonist R-Baclofen Reverses Altered Auditory Reactivity and Filtering in the Knock-Out Rat.GABA受体激动剂R-巴氯芬可逆转基因敲除大鼠听觉反应性和听觉过滤的改变。
Front Integr Neurosci. 2021 Aug 20;15:710593. doi: 10.3389/fnint.2021.710593. eCollection 2021.
5
Behavioral Battery for Testing Candidate Analgesics in Mice. I. Validation with Positive and Negative Controls.用于在小鼠中测试候选镇痛剂的行为学电池。I. 阳性和阴性对照的验证。
J Pharmacol Exp Ther. 2021 May;377(2):232-241. doi: 10.1124/jpet.120.000464. Epub 2021 Feb 23.
6
The loss of slow skeletal muscle isoform of troponin T in spindle intrafusal fibres explains the pathophysiology of Amish nemaline myopathy.梭内肌纤维中慢骨骼肌肌钙蛋白 T 同工型的缺失解释了阿什肯纳兹型先天性肌营养不良的病理生理学。
J Physiol. 2019 Aug;597(15):3999-4012. doi: 10.1113/JP278119. Epub 2019 Jul 3.
7
Azemiopsin, a Selective Peptide Antagonist of Muscle Nicotinic Acetylcholine Receptor: Preclinical Evaluation as a Local Muscle Relaxant.阿佐米星,一种肌肉型烟碱型乙酰胆碱受体的选择性肽拮抗剂:作为局部肌肉松弛剂的临床前评估。
Toxins (Basel). 2018 Jan 7;10(1):34. doi: 10.3390/toxins10010034.
8
Muscle power during intravenous sedation.静脉镇静期间的肌肉力量。
Jpn Dent Sci Rev. 2017 Nov;53(4):125-133. doi: 10.1016/j.jdsr.2017.02.001. Epub 2017 Mar 9.
9
Activation of the NLRP3 Inflammasome Is Associated with Valosin-Containing Protein Myopathy.NLRP3炎性小体的激活与含缬酪肽蛋白肌病相关。
Inflammation. 2017 Feb;40(1):21-41. doi: 10.1007/s10753-016-0449-5.
10
Dexmedetomidine ameliorates nocifensive behavior in humanized sickle cell mice.右美托咪定改善人源化镰状细胞小鼠的伤害性防御行为。
Eur J Pharmacol. 2015 May 5;754:125-33. doi: 10.1016/j.ejphar.2015.02.027. Epub 2015 Feb 25.
可乐定及其他咪唑烷类药物的低温效应与其进入小鼠中枢神经系统的能力的关系。
Eur J Pharmacol. 1981 Feb 19;69(4):477-82. doi: 10.1016/0014-2999(81)90452-0.
4
A new method for quantitative grip strength evaluation.一种用于定量握力评估的新方法。
Eur J Pharmacol. 1969;6(3):353-6. doi: 10.1016/0014-2999(69)90197-6.
5
A comparative study of dantrolene sodium and other skeletal muscle relaxants with the Straub tail mouse.用斯特劳布尾小鼠对丹曲林钠和其他骨骼肌松弛剂进行的对比研究。
Neuropharmacology. 1974 Mar;13(3):211-4. doi: 10.1016/0028-3908(74)90109-9.
6
Dantrolene, a direct acting skeletal muscle relaxant.丹曲林,一种直接作用的骨骼肌松弛剂。
J Pharm Sci. 1973 Jun;62(6):948-51. doi: 10.1002/jps.2600620619.
7
Learned taste aversions in rats as a function of dosage, concentration, and route of administration of LiCl.大鼠习得性味觉厌恶与氯化锂剂量、浓度及给药途径的关系
Physiol Behav. 1973 Jan;10(1):73-8. doi: 10.1016/0031-9384(73)90089-9.
8
Effects of morphine on striatal dopamine metabolism: possible mechanism of its opposite effect on locomotor activity in rats and mice.
Eur J Pharmacol. 1974 Apr;26(1):41-50. doi: 10.1016/0014-2999(74)90072-7.
9
Pharmacology of a new centrally acting muscle relaxant (RJ-64).一种新型中枢性肌肉松弛剂(RJ - 64)的药理学
Arzneimittelforschung. 1970 Nov;20(11):1778-83.
10
Testing the statistical certainty of a response to increasing doses of a drug.测试对药物剂量增加的反应的统计确定性。
Biometrics. 1985 Mar;41(1):295-301.