• 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

围产期营养不良大鼠长期治疗后缺乏神经元适应性变化。

Lack of neuronal adaptive changes following chronic treatments in perinatally undernourished rats.

作者信息

Keller E A, Molina V A, Orsingher O A

机构信息

Departamento de Farmacología, Facultad de Ciencias Químicas Universidad Naçional de Córdoba, Argentina.

出版信息

Pharmacol Biochem Behav. 1990 Dec;37(4):675-8. doi: 10.1016/0091-3057(90)90545-s.

DOI:10.1016/0091-3057(90)90545-s
PMID:1965513
Abstract

Reactivity of presynaptic dopaminergic and alpha 2-adrenoceptors following repeated stress or desipramine treatment was investigated by means of apomorphine (APO)- or clonidine (CLO)-induced hypoactivity, respectively, in adult rats undernourished at perinatal age. Under basal conditions, a comparable hypoactive response was observed in control and experimental animals following either APO or CLO administration. Chronic DMI or repeated immobilization sessions attenuated the hypoactivity elicited by APO or CLO in control animals; however, this effect was not observed in experimental rats. These findings demonstrate that deprived animals show impairment to produce neuronal adaptive changes in response to appropriate stimuli, which may account for the behavioral alterations attributed to early undernutrition.

摘要

通过阿扑吗啡(APO)或可乐定(CLO)诱导的活动减退,分别研究围产期营养不良的成年大鼠在反复应激或地昔帕明治疗后突触前多巴胺能和α2-肾上腺素能受体的反应性。在基础条件下,给予APO或CLO后,对照动物和实验动物均观察到类似的活动减退反应。慢性地昔帕明(DMI)或反复固定应激会减弱对照动物中APO或CLO诱导的活动减退;然而,在实验大鼠中未观察到这种效应。这些发现表明,营养缺乏的动物在对适当刺激作出反应时,产生神经元适应性变化的能力受损,这可能解释了早期营养不良所致的行为改变。

相似文献

1
Lack of neuronal adaptive changes following chronic treatments in perinatally undernourished rats.围产期营养不良大鼠长期治疗后缺乏神经元适应性变化。
Pharmacol Biochem Behav. 1990 Dec;37(4):675-8. doi: 10.1016/0091-3057(90)90545-s.
2
Increased neuronal activity in locus coeruleus from adult rats undernourished at perinatal age: its reversal by desipramine.围产期营养不良的成年大鼠蓝斑中神经元活动增加:地昔帕明可使其恢复正常。
Life Sci. 2001 Oct 12;69(21):2551-9. doi: 10.1016/s0024-3205(01)01335-2.
3
Opiate agonist-induced changes in behavioral sensitivity to clonidine are observed in perinatally malnourished rats exposed to chronic stress.在暴露于慢性应激的围产期营养不良大鼠中,观察到阿片类激动剂诱导的对可乐定行为敏感性的变化。
Pharmacol Biochem Behav. 1998 May;60(1):1-5. doi: 10.1016/s0091-3057(97)00059-2.
4
Immobilization stress modifies locomotor response to catecholamine receptor agonists in rats.制动应激改变大鼠对儿茶酚胺受体激动剂的运动反应。
Pol J Pharmacol Pharm. 1988 Sep-Oct;40(5):441-50.
5
Adaptive changes in alpha-2 adrenoceptor mediated responses: analgesia, hypothermia and hypoactivity.α-2肾上腺素能受体介导反应的适应性变化:镇痛、体温过低和活动减退。
Pharmacol Toxicol. 1989 Aug;65(2):143-51. doi: 10.1111/j.1600-0773.1989.tb01145.x.
6
Sex-related differences in central adrenergic function and responsiveness to repeated administration of desipramine or electroconvulsive shock.中枢肾上腺素能功能以及对重复给予地昔帕明或电休克反应的性别差异。
Br J Pharmacol. 1989 May;97(1):111-8. doi: 10.1111/j.1476-5381.1989.tb11930.x.
7
Chronic stress-induced changes in locus coeruleus neuronal activity.慢性应激引起的蓝斑核神经元活动变化。
Brain Res Bull. 1990 Feb;24(2):293-6. doi: 10.1016/0361-9230(90)90219-p.
8
Effects of long-term desipramine administration on noradrenergic neurotransmission: electrophysiological studies in the rat brain.长期给予地昔帕明对去甲肾上腺素能神经传递的影响:大鼠脑内的电生理研究
J Pharmacol Exp Ther. 1991 Jun;257(3):1081-90.
9
ACTH accelerates the attenuation of alpha 2-adrenoceptors response in nucleus accumbens following chronic desipramine.
Methods Find Exp Clin Pharmacol. 1992 Apr;14(3):189-92.
10
Adrenocorticotropic hormone influences the development of adaptive changes in dopamine autoreceptors induced by chronic administration of desipramine.促肾上腺皮质激素影响由慢性给予地昔帕明诱导的多巴胺自身受体适应性变化的发展。
Neuropharmacology. 1991 Jul;30(7):719-25. doi: 10.1016/0028-3908(91)90179-f.