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1.
目的:观察大鼠在不同时间水环境应激过程中下丘脑、纹状体5-羟色胺(5-HT)及其代谢产物5-羟吲哚乙酸(5-HMA)含量的变化,分析5-HT含量变化与水环境之间的关系。方法:分别测定安静组、一次水环境组和长期水环境组大鼠8周后下丘脑、纹状体中5-HT和5-mAA含量。结果:长期水环境组大鼠下丘脑5-HT含量显著高于安静组(P〈0.05),一次水环境组大鼠纹状体5-mAA含量显著高于安静组(P〈O.05),其余各组间无显著性差异,但水环境的影响可使上述指标较安静组有增高的趋势。结论:水环境刺激可使大鼠下丘脑、纹状体中的抑制性神经递质5-HT及其代谢产物的含量增加,使机体处于中枢抑制状态。  相似文献   

2.
力竭运动对大鼠脑纹状体5-HT含量及其代谢的影响   总被引:1,自引:0,他引:1  
目的:观察力竭运动对大鼠脑纹状体5-羟色胺(5-HT)含量及其代谢的影响,分析纹状体中5-HT合成代谢和分解代谢中各指标的关系,进一步探讨力竭运动后脑5-HT含量及其代谢的动态变化对运动性中枢疲劳发生、发展的影响并分析其机理。方法:大鼠分为两组。力竭运动组大鼠进行一次性游泳运动直至力竭。断头处死,取纹状体测色氨酸(Trp)、5-HT和5-羟吲哚乙酸(5-HIAA)含量,测色氨酸羟化酶(TPH)和单胺氧化酶(MAO)活性,取血清测游离色氨酸(f-Trp)含量。结果:与安静组5-HT含量及其代谢各指标相比,力竭运动组大鼠血清f-Trp含量有下降趋势,其余各指标均呈升高趋势,其中纹状体Trp(P<0.01)和5-HIAA(P<0.001)含量显著升高。结论:(1)力竭运动引起血清Trp透过血脑屏障进入脑中增多,导致血清f-Trp含量下降且纹状体Trp含量增多,激活TPH的活性,增强脑5-HT的合成。(2)运动中5-HT的分解也是增加的,说明力竭运动使5-HT代谢加快,易产生中枢疲劳。提示力竭运动组大鼠在力竭运动后,中枢神经系统抑制过程占优势。  相似文献   

3.
目的:探讨游泳运动对大鼠纹状体、下丘脑(DA)内多巴胺的含量及其代谢的影响.方法:选取72只雄性SD大鼠,随机分成6组:安静对照组(A)、一次性力竭游泳运动组(B)、安静+水环境组(C)、游泳耐力训练组(D)、水环境组(E)、游泳耐力训练后一次性力竭游泳运动组(F).D组按照耐力训练方案进行负重训练,每周5次,持续7周.所有大鼠一起断头处死,各组交叉进行,迅速取出脑组织(纹状体、下丘脑)进行多巴胺浓度和单胺氧化酶B(MAO-B)活性的测试.结果:一次性力竭运动或游泳训练对下丘脑中DA含量或MAO-B活性的影响无明显影响,而纹状体DA浓度在一次性力竭运动尤其是游泳训练后都明显升高(P〈0.05),MAO-B也有升高的趋势.结论:一次性力竭运动尤其是游泳耐力训练使DA的浓度和MAO-B活性增加,其合成和分解代谢都增加,提高了DA的转换率,以适应运动的需要,有利于改善脑机能,延缓运动疲劳,是适应运动的表现.  相似文献   

4.
50只SD雄性成年大鼠分别接受不同时间的水应激、一次性力竭游泳运动和长期游泳耐力训练,用免疫印迹法检测中脑TH含量,以荧光发光分析法检测纹状体DA含量。结果显示:长期游泳训练与安静状态的大鼠和一次性力竭游泳大鼠相比中脑TH含量有升高的趋势,但以上变化并没有显著性差异;而一次性力竭游泳运动使得大鼠纹状体DA含量高与安静组,长期游泳耐力训练引起了大鼠纹状体DA含量显著性升高;处于一次性水环境与长期水环境的大鼠中脑TH与纹状体DA含量无显著性差异;长期耐力游泳训练大鼠中脑TH和纹状体DA含量显著性高于处于水环境的大鼠。提示:一次性力竭游泳运动抑制了中脑TH活性,而长期游泳耐力训练有助于提高大鼠中脑TH含量,增加纹状体DA的释放量,提高中枢兴奋性,从而能够改善中枢机能,延迟中枢疲劳的发生时间;水环境会抑制大鼠中脑TH含量,从而使机体处于中枢抑制状态,建议在建立大鼠游泳训练模型中,应增列水环境对照组,从而增强实验的可比性与真实性。  相似文献   

5.
[目的]观察整肤疗法对运动性疲劳大鼠下丘脑单胺类神经递质的影响,以探索整肤疗法对中枢神经系统的作用机制.[方法]将40只SD雄性大鼠随即分成安静对照组、运动后即刻处死组、运动后自然恢复组及运动后整肤治疗组.除安静组外,其余组游泳运动至疲劳,即刻组立即处死取下丘脑,自然恢复组休息30min,整肤疗法组施以整肤治疗(提拉皮肤刺激)30min,两组均断头处死取出下丘脑,采用高效液相色谱一电化学检测法检测各组大鼠下丘脑中5-羟色胺(5-HT)和多巴胺(DA)水平.[结果]大鼠运动性疲劳后,下丘脑中的5-HT水平明显升高,DA水平则较明显降低;经过整肤治疗后,5-HT和DA水平虽然变化不明显,但是5-HT水平比自然恢复组低,DA水平已经比运动后即刻略有回升.[结论]整肤疗法在短时间内对运动性疲劳大鼠下丘脑中5-HT和DA水平的影响不明显,但能看出有促进疲劳恢复的趋势.  相似文献   

6.
目的:通过观察耳针对脑缺血后睡眠剥夺大鼠下丘脑单胺类神经递质和细胞因子IL-1β的影响,探讨耳针治疗卒中后失眠的作用机制.方法:取SPF级Wistar雄性大鼠,用Zea Logna等报道的大脑中动脉栓线法(MCAO)制备大脑中动脉闭塞再灌注模型,模型成功后将动物随机分为对照组、模型组、安定组和耳针组4组,再对除对照组外的其他3组动物腹腔注射对氯苯丙氨酸(PCPA)造成脑缺血后睡眠剥夺大鼠模型,安定组每日腹腔注射安定,耳针组取耳穴神门(TF4)进行皮内针埋藏,均连续治疗7 d.采用酶联免疫吸附测定法(ELISA)检测下丘脑单胺类神经递质5-羟色胺(5-HT)、5-羟引哚乙酸(5-HIAA)、多巴胺(DA)、去甲肾上腺素(NE)和白介素-1β(IL-1β)的含量.结果:与对照组相比模型组大鼠下丘脑5-HT、5-HIAA和IL-1β含量减低(P0.05),DA、NE含量显著升高(P0.01);与模型组相比安定组与耳针组大鼠下丘脑5-HT和IL-1β含量显著升高(P0.01),DA、NE含量显著降低(P0.01).结论:耳针治疗卒中后失眠可能通过提高机体下丘脑5-HT、5-HIAA及细胞因子IL-1β含量,降低NE和DA的含量以调节和改善睡眠.  相似文献   

7.
目的:观察不同穴位处方麦粒灸对失眠大鼠下丘脑5-羟色胺(5-HT)、5-羟吲哚乙酸(5-HIAA)、去甲肾上腺素(NE)、多巴胺(DA)质量分数的变化,探讨麦粒灸治疗失眠症的作用机理.方法:将SD大鼠36只随机分为6组即对照组、模型组、安定组、麦粒灸1组(取百会、神道、心俞穴),麦粒灸2组(取三阴交、神门穴),麦粒灸3组(取申脉、照海穴),模型组以腹腔注射对氯苯丙氨酸(PCPA)建立大鼠失眠模型,安定组给予腹腔注射安定,麦粒灸各组分别按穴位给予麦粒灸治疗,每组连续治疗6 d后检测大鼠下丘脑5-HT、5-HIAA、NE、DA的变化.结果:模型组5-HT和5-HIAA质量分数明显低于对照组(P<0.01);麦粒灸各组5-HT、5-HIAA明显升高,NE、DA明显降低,与模型组和安定组比较差异有显著性(P<0.05,P<0.01);麦粒灸各组之间比较,麦粒灸2组优于麦粒灸1组(P<0.05),麦粒灸3组与麦粒灸1组、麦粒灸2组比较均无显著性差异(P>0.05).结论:麦粒灸可能是通过提高失眠大鼠下丘脑5-HT、5-HIAA质量分数,降低NE、DA质量分数而改善睡眠;麦粒灸2组作用优于麦粒灸1组,说明取三阴交、神门穴治疗失眠症疗效更好.  相似文献   

8.
运用文献资料法,系统地概括了脑内5-羟色胺(5-hydroxytryptamine,5-HT)及其受体的特性,并总结了近年来脑内5-HT及受体与运动的研究现状:1.5-HT作为一种抑制性神经递质可以降低从中枢向外周发放的冲动,导致中枢疲劳。2.5-HT的升高可能首先发生在某一脑区而非全脑。3.耐力运动中大脑5-HT含量升高且在疲劳时加剧。4.力竭运动可同时加快5-HT的合成和降解速度,脑内5-HT在运动即刻几乎没有明显变化。5.5-HT受体各亚型存在较大差异,有的起抑制性作用,有的则发挥兴奋性作用。  相似文献   

9.
目的研究长期耐力训练对雄性大鼠肾组织一氧化氮(NO)、一氧化氮合酶(NOS)的影响.方法64只雄性Wistar大鼠随机分为2组:对照组和耐力组.每组32只.耐力组进行8周跑台训练,对照组一直笼中饲养不训练.耐力组8周训练结束后,对照组和耐力组2组大鼠分别在直径70 cm的圆形塑料桶中进行2天适应性游泳,水深55 cm,水温32℃,每天15 min.第3天,两组大鼠分别于安静、游泳40 min、游泳力竭即刻、力竭后恢复24 h,4种状态麻醉处死取材,每种状态8只大鼠.安静状态大鼠不进行游泳直接取材,其余状态大鼠尾部负重3%体重的铅条,在圆形塑料桶中进行游泳.游泳40 min状态大鼠统一在游泳至40 min后取材.游泳力竭即刻状态大鼠统一在游泳至力竭即刻取材.力竭后恢复24 h状态大鼠从被确定为力竭后计时,经过24 h后取材.测定NO含量和NOS活性.结果耐力组与对照组相比,力竭即刻状态,耐力组NO含量极显著升高(P0.01);在24 h恢复后,耐力组NO含量极显著升高(P0.01).游泳40 min状态,耐力组NOS活性极显著降低(P0.01);力竭即刻状态,耐力组NOS活性显著降低(P0.05);在24 h恢复后,耐力组NOS活性极显著升高(P0.01).结论长期耐力训练增加了力竭即刻肾组织的NO含量,减轻缺血症状,增加了24h恢复期NO含量;长期耐力训练减小了运动过程中和力竭即刻肾组织NOS活性的升高幅度;增加了24 h恢复期NOS活性,对肾组织再灌注期的恢复有积极意义.  相似文献   

10.
研究常规训练对大鼠淋巴细胞内Ca^2 浓度的影响,并与未训练大鼠进行比较。将24只大鼠随机分为安静组、力竭运动组和训练 力竭运动组。训练 力竭运动组常规训练3周后,与力竭运动组一同进行负重4%条件下的力竭游泳运动。观察、对照运动后即刻大鼠脾细胞、胸腺细胞及外周血淋巴细胞内Ca^2 浓度的变化,结果发现训练 力竭运动组达到力竭的时间较力竭运动组显著延长。与安静组相比,力竭运动组脾细胞及外周血淋巴细胞内Ca^2 滚度有升高趋势,而训练 力竭运动组升高显著;训练 力竭运动组3种淋巴细胞内Ca^2 浓度普遍有高于力竭运动组的趋势,表明运动训练能提高大鼠运动能力可能与增强机体对力竭运动导致的钙调节失衡的适应能力有关。  相似文献   

11.
目的观察五参胶囊(Wu Shen Capsules,WSh C)对小鼠镇静催眠作用的影响,并探讨其作用机制.方法将ICR小鼠随机分为对照组、五参胶囊高剂量组、中剂量组和低剂量组.五参胶囊高剂量组用药量为200 mg/(kg·d~(-1)),中剂量组用药量为100 mg/(kg·d~(-1)),低剂量组用药量为50 mg/(kg·d~(-1)),给药时间为15 d,于给药结束后进行小鼠自主活动实验和协同戊巴比妥钠阈上剂量睡眠时间实验,测定5 min内各组小鼠的活动次数和站立次数,记录各组小鼠的睡眠潜伏期和睡眠持续时间.采用酶联免疫吸附法检测小鼠下丘脑5-羟色胺(5-Hydroxytryptamine,5-HT)、5-羟吲哚乙酸(5-Hydroxyindole acetic acid,5-HIAA)、γ-氨基丁酸(γ-aminobutyric acid,GABA)、谷氨酸(glutamine,Glu)含量,并计算5-HIAA/5-HT比值及Glu/GABA比值.结果与对照组比较,WSh C各给药组小鼠活动次数减少,睡眠潜伏期缩短,睡眠持续时间延长(P0.01),WSh C能升高小鼠下丘脑5-HIAA含量和5-HIAA/5-HT比值,降低Glu含量和Glu/GABA比值.结论 WSh C具有明显镇静催眠作用,其机制可能与调节中枢兴奋性和抑制性神经递质有关.  相似文献   

12.
G J Kilpatrick  B J Jones  M B Tyers 《Nature》1987,330(6150):746-748
Functional serotonin (5-hydroxytryptamine, 5-HT) receptors have been divided into three subtypes: 5-HT1-like, 5-HT2 and 5-HT3 (ref. 1). Brain binding sites have been identified for both the 5-HT1 and 5-HT2 subtypes. Receptors of the 5-HT3 type have been characterized on isolated peripheral tissue models such as the rat vagus nerve, guinea-pig ileum and isolated rabbit heart. Using these models, selective 5-HT3 receptor antagonists such as MDL 72222 (ref. 5), ICS 205-930 (ref. 6), GR38032F (ref. 7) and BRL 43694 (ref. 8) have been developed. Recently, GR38032F, MDL 72222 and ICS 205-930 have been shown to have behavioural effects in rodents and primates that undoubtedly reflect an action in the central nervous system (refs 9-11 and unpublished observations), suggesting the existence of 5-HT3 receptors in the brain. Here we report direct evidence for the existence of 5-HT3 receptors in rat brain tissue and their distribution, based on high affinity binding of the potent 5-HT3 receptor antagonist 3H-GR65630 to homogenates of rat entorhinal cortex. Selective 5-HT3 receptor antagonists and agonists inhibited binding of 3H-GR65630 with high affinities which correlated well with their actions on the rat isolated vagus nerve. Binding was differentially distributed throughout the brain with high concentrations in cortical and limbic areas.  相似文献   

13.
红景天苷对运动疲劳大鼠神经递质影响研究   总被引:3,自引:0,他引:3  
观察高山红景天苷对运动性疲劳大鼠中枢单胺类神经递质DA、5-HT、5-HIAA、NE质量比的影响,探讨其抗运动性疲劳的机制.将Wistar大鼠随机分成4组,每组10只,分别为阴性对照组(生理盐水);高山红景天苷低剂量组、中剂量组和高剂量组,建立中枢疲劳模型,分别灌胃给药,取大脑组织制备样本,检测神经递质DA、5-HT、...  相似文献   

14.
To investigate the effect on central nervous transmission of toosendanin (TSN), a presynaptic blocker, rat striatum was perfusedin vivo with a TSN-containing artificial cerebrospinal fluid (ACSF) and the level of dopamine (DA) as well as related metabolites in the collected dialysates has been determined by a microbore HPLC with electrochemical detection (microbore HPLC-ECD). The results are as follows: ( i ) TSN induced a biphasic change of DA from its basal level;( ii ) the basal contents of two metabolites, 3,4-dihydroxyphenylacetic acid (DOPAC) and homovanillic acid (HVA) increased in turn and stayed at a higher level than basal control for a long period. The basal level of 5-hydroxyindoleacetic acid (5-HIAA), a metabolite of 5-hydroxytryptamine(5-HT), had a change similar to that of HVA; ( iii ) after perfusion with TSN-containing ACSF, high K+-evoked DA release was inhibited. These results show that TSN does not selectively affect acetylcholine (ACh) release, but probably acts on a common mechanism responsible for transmitter release at different synapses by interfering with the proteins involved in fusian and resulting in diffusion of the vesicular contents into the cytoplasm and blockade of normal exocytosis.  相似文献   

15.
Orphanin FQ (OFQ) is a new modulatory peptide which was found in 1994. It mediates in morphine analgesia and electroacupuncture analgesia. The interaction between OFQ and 5-hydroxytryptamine (5-HT) on analgesia was observed using the method of intracere-broventricular microinjection. The results showed that cumulative i. c. v. administration of gradually increasing doses of 5-HT produced a dose-dependent analgesia, and administration of different doses of OFQ separateness had no significant effect on tail flick latency, but 1 or 10 μg OFQ could reverse the analgesia induced by 5-HT, suggesting that OFQ could antagonize the analgesia induced by 5-HT in rat brain.  相似文献   

16.
H Gozlan  S El Mestikawy  L Pichat  J Glowinski  M Hamon 《Nature》1983,305(5930):140-142
Binding studies with appropriate labelled ligands have revealed the existence of two types of serotonin (5-HT) receptor, 5-HT1 and 5-HT2, in the central nervous system of mammals. The 5-HT1 type is characterized by a higher affinity for agonists than for antagonists, whereas the 5-HT2 type binds preferentially to antagonists. However, neither of these receptor types apparently corresponds to the presynaptic autoreceptor controlling 5-HT release. In an attempt to identify the presynaptic autoreceptor directly, we synthesized the tritiated derivative of 8-hydroxy-2-(di-n-propylamino) tetralin (PAT), a new tetralin derivative with potent 5-HT agonist properties and carried out binding studies with rat brain membranes. As we report here, in the hippocampus, the properties of 3H-PAT binding sites correspond closely to those of 5-HT1 sites. In contrast, in the striatum, 3H-PAT binding sites exhibit a subcellular distribution and pharmacological characteristics usually associated with presynaptic autoreceptors. Furthermore, a marked loss of 3H-PAT binding sites occurs in the striatum (but not in the hippocampus) after the selective degeneration of serotoninergic fibres in 5,7-hydroxytryptamine (5,7-HT)-treated rats. Conversely, the sprouting of additional 5-HT terminals in the brain stem of adult rats treated at birth with 5,7-HT is associated with an increased density of 3H-PAT binding sites in this region. 3H-PAT thus seems to be a useful ligand for studying the biochemical and pharmacological characteristics of presynaptic autoreceptors in selected regions of rat brain.  相似文献   

17.
采用平板培养计数法检测大鼠肠道细菌,采用高效液相色谱紫外分光法检测大鼠血中5-HT含量,研究了部分肝切除大鼠肠腔细菌数量的变化及其对肠道5-HT分泌的影响.结果表明:与对照组相比,部分肝切除后0h、2h、6h、12h、24h、48h及72h各时间点肠道细菌数和血中5-HT含量显著增多(P<0.05或0.01);部分肝切除并灌服硫酸庆大霉素的大鼠与部分肝切除的大鼠相比,肠道细菌数和血中5-HT含量均显著减少(P<0.05或0.01).部分肝切除后肠道细菌的增多可能是5-HT分泌量增加的机制之一.  相似文献   

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