氯胺酮加与不加噻嗪对犬血液学和生理的影响

G. Yohannes
{"title":"氯胺酮加与不加噻嗪对犬血液学和生理的影响","authors":"G. Yohannes","doi":"10.19080/IJCSMB.2018.05.555654","DOIUrl":null,"url":null,"abstract":"Ketamine hydrochloride is a dissociative anesthetic of the cyclohexylamine group used for chemical restraint and for the induction and maintenance of anesthesia in a number of species. Unlike many anesthetics, ketamine usually stimulates cardiovascular function in normal animals, causing increase in heart rate (HR) and mean arterial pressure (MAP). The use of ketamine as a sole anesthetic has been limited by muscle hypertonicity and myoclonus, violent recovery and occasional occurrence of convulsions [1]. Ketamine is combined with an alpha-2-agonist (e.g. xylazine), a benzodiazepine (e.g. diazepam) or a phenothiazine tranquillizer (e.g. acepromazine) to enhance muscle relaxation, analgesia, to prevent seizures/convulsions and prolong the duration of anesthetic effect. It is associated with a rapid onset, good to excellent sedation of one to two hours duration, excellent analgesia and smooth recovery. The analgesia and sedation are due to central nervous system depression and the muscle relaxation is due to the central inhibition of intraneural transmission [2]. Ketamine is poor in visceral analgesia. However, it can be used in combination with xylazine or diazepam to provide good visceral analgesia in case of abdominal surgery (including ovariohysterectomy) and thoracic surgery. Pain is an unpleasant sensory or emotional experience most commonly associated with potential tissue damage. The sensation of pain is a consequence of the activation of specialized receptors and neurological pathways after such pain stimuli [3,4]. Xylazine, an alpha-2 agonist used in animal experiments, stimulates alpha-2 adrenergic receptor in cerebral presynaptic nerve ends, inhibits release of catecholamines and dopamine resulting in analgesic and sedative eff ects, and hinders nerve conduction in the central nervous system leading to relaxation of striated muscles. Xylazine is usually used in combination with ketamine during anesthetic applications [5].","PeriodicalId":93190,"journal":{"name":"International journal of cell science & molecular biology","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2018-08-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"5","resultStr":"{\"title\":\"Hematological and Physiological Effects of Ketamine with and without Xylazine in Dogs\",\"authors\":\"G. Yohannes\",\"doi\":\"10.19080/IJCSMB.2018.05.555654\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Ketamine hydrochloride is a dissociative anesthetic of the cyclohexylamine group used for chemical restraint and for the induction and maintenance of anesthesia in a number of species. Unlike many anesthetics, ketamine usually stimulates cardiovascular function in normal animals, causing increase in heart rate (HR) and mean arterial pressure (MAP). The use of ketamine as a sole anesthetic has been limited by muscle hypertonicity and myoclonus, violent recovery and occasional occurrence of convulsions [1]. Ketamine is combined with an alpha-2-agonist (e.g. xylazine), a benzodiazepine (e.g. diazepam) or a phenothiazine tranquillizer (e.g. acepromazine) to enhance muscle relaxation, analgesia, to prevent seizures/convulsions and prolong the duration of anesthetic effect. It is associated with a rapid onset, good to excellent sedation of one to two hours duration, excellent analgesia and smooth recovery. The analgesia and sedation are due to central nervous system depression and the muscle relaxation is due to the central inhibition of intraneural transmission [2]. Ketamine is poor in visceral analgesia. However, it can be used in combination with xylazine or diazepam to provide good visceral analgesia in case of abdominal surgery (including ovariohysterectomy) and thoracic surgery. Pain is an unpleasant sensory or emotional experience most commonly associated with potential tissue damage. The sensation of pain is a consequence of the activation of specialized receptors and neurological pathways after such pain stimuli [3,4]. Xylazine, an alpha-2 agonist used in animal experiments, stimulates alpha-2 adrenergic receptor in cerebral presynaptic nerve ends, inhibits release of catecholamines and dopamine resulting in analgesic and sedative eff ects, and hinders nerve conduction in the central nervous system leading to relaxation of striated muscles. Xylazine is usually used in combination with ketamine during anesthetic applications [5].\",\"PeriodicalId\":93190,\"journal\":{\"name\":\"International journal of cell science & molecular biology\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2018-08-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"5\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International journal of cell science & molecular biology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.19080/IJCSMB.2018.05.555654\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International journal of cell science & molecular biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.19080/IJCSMB.2018.05.555654","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 5

摘要

盐酸氯胺酮是一种解离性环己胺类麻醉剂,在许多物种中用于化学抑制和诱导和维持麻醉。与许多麻醉药不同,氯胺酮通常会刺激正常动物的心血管功能,导致心率(HR)和平均动脉压(MAP)增加。氯胺酮作为单一麻醉剂的使用受到肌肉高张力和肌阵挛、剧烈恢复和偶尔发生惊厥的限制。氯胺酮与α -2激动剂(如二嗪)、苯二氮卓类药物(如地西泮)或吩噻嗪类镇静剂(如乙酰丙嗪)联合使用,以增强肌肉松弛、镇痛、防止癫痫发作/抽搐并延长麻醉作用的持续时间。它与快速起效,一至两小时的良好至优异的镇静作用,良好的镇痛作用和顺利恢复有关。镇痛和镇静作用是由于中枢神经系统的抑制,肌肉松弛是由于中枢抑制神经内传递[2]。氯胺酮在内脏镇痛方面效果不佳。但在腹部手术(包括卵巢子宫切除术)和胸外科手术中,可与噻嗪或地西泮合用,提供良好的内脏镇痛效果。疼痛是一种不愉快的感觉或情绪体验,通常与潜在的组织损伤有关。痛觉是痛觉刺激后特定受体和神经通路激活的结果[3,4]。甲拉嗪是一种用于动物实验的α -2激动剂,刺激大脑突触前神经末梢α -2肾上腺素能受体,抑制儿茶酚胺和多巴胺的释放,产生镇痛和镇静作用,阻碍中枢神经系统的神经传导,使横纹肌松弛。在麻醉应用中,噻嗪通常与氯胺酮联合使用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hematological and Physiological Effects of Ketamine with and without Xylazine in Dogs
Ketamine hydrochloride is a dissociative anesthetic of the cyclohexylamine group used for chemical restraint and for the induction and maintenance of anesthesia in a number of species. Unlike many anesthetics, ketamine usually stimulates cardiovascular function in normal animals, causing increase in heart rate (HR) and mean arterial pressure (MAP). The use of ketamine as a sole anesthetic has been limited by muscle hypertonicity and myoclonus, violent recovery and occasional occurrence of convulsions [1]. Ketamine is combined with an alpha-2-agonist (e.g. xylazine), a benzodiazepine (e.g. diazepam) or a phenothiazine tranquillizer (e.g. acepromazine) to enhance muscle relaxation, analgesia, to prevent seizures/convulsions and prolong the duration of anesthetic effect. It is associated with a rapid onset, good to excellent sedation of one to two hours duration, excellent analgesia and smooth recovery. The analgesia and sedation are due to central nervous system depression and the muscle relaxation is due to the central inhibition of intraneural transmission [2]. Ketamine is poor in visceral analgesia. However, it can be used in combination with xylazine or diazepam to provide good visceral analgesia in case of abdominal surgery (including ovariohysterectomy) and thoracic surgery. Pain is an unpleasant sensory or emotional experience most commonly associated with potential tissue damage. The sensation of pain is a consequence of the activation of specialized receptors and neurological pathways after such pain stimuli [3,4]. Xylazine, an alpha-2 agonist used in animal experiments, stimulates alpha-2 adrenergic receptor in cerebral presynaptic nerve ends, inhibits release of catecholamines and dopamine resulting in analgesic and sedative eff ects, and hinders nerve conduction in the central nervous system leading to relaxation of striated muscles. Xylazine is usually used in combination with ketamine during anesthetic applications [5].
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信