Serotonin Enhances Striatal Dopamine Outflow In Vivo Through Dopamine Uptake Sites

Abstract: Serotonin (5-HT) administered at 1, 3, and 10 µ M into the striatum of halothane-anesthetized rats by in vivo microdialysis increased extracellular dopamine (DA) in a concentration-dependent manner (approximately 65, 190, and 440%, respectively). These effects were reduced by 50% in the presence of 1 µ M tetrodotoxin (TTX) or in the absence of Ca²⁺ ions. The DA uptake blocker nomifensine (0.1 µ M ) significantly lowered (by 50%) the enhancement of DA outflow induced by 3 µ M 5-HT. Nomifensine (1 µ M ) coperfused with 1 µ M TTX abolished the 1 and 3 µ M 5-HT-induced DA outflow, whereas the effect of 10 µ M 5-HT was significantly reduced by 1 (−55%) and 10 µ M (−70%) nomifensine. These data demonstrate that, in vivo, striatal DA uptake sites are partially involved in the DA-releasing action of 5-HT.     

Nitric oxide (NO) as an intermediate in the cryptogein-induced hypersensitive response--a critical re-evaluation

A hypersensitive response (HR) was induced in tobacco leaves and cell suspensions by the fungal elicitor cryptogein, and NO production was followed by chemiluminescence and occasionally by diaminofluorescein (DAF)-fluorescence. Results from both methods were at least partly consistent, but kinetics was different. NO emission was not induced by cryptogein in leaves, whereas in cell suspensions some weak NO emission was observed, which was nitrate reductase (NR)-dependent, but not required for cell death. Nitric oxide synthase (NOS) inhibitors did not prevent cell death, but PR-1 expression was weakened. In conclusion, neither NR nor NOS appear obligatory for the cryptogein-induced HR. However, a role for NO was still suggested by the fact that the NO scavenger cPTIO prevented the HR. Unexpectedly, cPTI, the reaction product of cPTIO and NO, also impaired the HR but without scavenging NO. Thus, prevention of the HR by cPTIO is not necessarily indicative for a role of NO. Further, even a 100-fold NO overproduction (over wild type) by a nitrite reductase-deficient mutant did not interfere with the cryptogein-induced HR. Accordingly, the role of NO in the HR should be reconsidered.     

栗斑腹鹀的栖息地和巢址选择

于1999到2001年5月至7月连续3a在吉林省镇赉县大岗林场,采用样地法和样方法,对栗斑腹鹀的栖息地选择和巢址选择进行了研究.结果表明此鸟的繁殖是在草甸草原+杏树环境下进行的,对栖息地样方和对照样方的对比分析得出,杏树最大高度、50 m半径圆内杏树数量、贝加尔针茅数量、大油芒数量、植物盖度、火绒草平均高度、贝加尔针茅最大高度、兴安胡枝子平均高度8个因子是影响其栖息地选择的主要因子.通过对46个巢的研究发现,大多数栗斑腹鹀把巢建在贝加尔针茅下面,巢出入口方向多为东南45°和西南45°.对46巢的27个因子的主成分分析,结果发现植物盖度、火绒草高度、鸢尾数量、巢出入口方向、10 m内杏树数量、30 m内杏树数量、裸地面积这6个因子是巢址选择的主要因子.对46巢26个巢址和非巢址因子进行判别分析,植物盖度、大油芒、乳浆大戟高度、石竹数量、线叶菊高度和30m内杏树数量等6个因子,为巢位选择的主要因子 .两种分析结果基本相似.总之,栗斑腹鹀喜欢在植被盖度大、杏树相对多、贝加尔针茅和大油芒的密度大、食物资源丰富的区域内营巢.     

影响灰脸鵟鹰巢址选择的主要生态因素

1996～1997年,在吉林省左家自然保护区及土门岭地带对灰脸鵟鹰(Butastur indicus)的巢树和巢址特点进行了系统研究。运用逐步判别分析的方法,通过对因子进入判别方程的先后顺序检测因子的重要性,通过对Wilk’sλ值的检测确定各因子对判别模型的贡献率,根据生态因子的重要性和贡献率大小确定影响灰脸鵟鹰巢址选择的主要生态因素。两年共观测灰脸鵟鹰的巢址12处,其中83．3％(n=10)位于山坡的上部位置,66．7％(n=8)位于山北坡;在灰脸鵟鹰所利用的巢树中,松科(Pinaceae)植物占的比例最大,为75％(n=9)。逐步判别分析结果表明,胸径大于30cm乔木的基面积、针叶林的基面积和灌木数量等生态因子是影响灰脸鵟鹰巢址选择的主要生态因素。     

力竭运动及恢复期大鼠纹状体5-HT、DA及其代谢物浓度的动态变化研究

目的:观察一次性力竭运动过程及恢复期大鼠纹状体细胞外液中多巴胺(DA)和5-羟色胺(5-HT)及其代谢物浓度的动态变化规律。方法:采用活体微透析结合毛细管电泳-激光诱导技术,连续观察清醒大鼠在一次性力竭运动过程及恢复期纹状体细胞外液中酪氨酸(Tyr)、5-HT、5-羟吲哚乙酸(5-HIAA)、色氨酸(Trp)和DA浓度的动态变化。结果:大鼠纹状体细胞外液中Trp、5-HT、5-HIAA水平运动初期均未见显著变化(P>0.05),运动后期、力竭及恢复期均显著高于安静水平(P<0.05,P<0.01);DA、Tyr水平在运动后期、力竭及恢复期显著高于安静水平(P<0.05,P<0.01);DA/5-HT运动初期显著升高(P<0.05,P<0.01),运动后期出现下降趋势,力竭前15 min降至最低点,而恢复期略有回升,但运动后期、力竭及恢复期与安静状态相比均无显著差异。结论:力竭运动过程中大鼠纹状体细胞外液中DA和5-HT的动态变化具有阶段性特征,运动疲劳过程中状体内DA和5-HT两种神经递质的代谢水平均显著增强,而其中以5-HT的作用占优。     

Hyperactivity and alteration of the midbrain dopaminergic system in maternally stressed male mice offspring

We recently demonstrated that prolonged maternal stress produces profound and long-lasting deficits in brain functions by programming a subset of target genes. We have now examined the possible effects of prenatal stress on the motility of adult offspring and dopamine (DA)-related gene expression in their midbrains, one of the target brain regions of stress hormones. Maternally stressed adult male mice showed impaired response habituation to novelty, and increased wheel-running activity associated with altered responses to DA receptor and DA transporter (DAT) blockers. Along with the behavioral changes, the expression profiles of several genes of the midbrain DAergic system appeared to be altered. Expression of DAT was reduced and expression of DA receptors and striatal DA-regulated neuropeptide genes was also affected. Taken together, the present findings indicate that maternal stress can cause hyperactivity in adult offspring associated with alterations in the midbrain DAergic system suggestive of a functional hyperdopaminergic state.     

alpha-MSH and Pro-Leu-Gly-NH2 (PLG; MIF-1): influence on dopamine (DA) uptake in crude synaptosomal preparations from rat mediobasal hypothalamus (MBH) and caudate putamen (CP)

The uptake of tritiated dopamine [3H] (DMI insensitive DA uptake) by synaptosomal fractions isolated from rat mediobasal hypothalamus (MBH) and caudate putamen (CP) was measured in the presence of different concentrations of alpha-melanocyte stimulating hormone (alpha-MSH) and Pro-Leu-Gly-NH2 (PLG; MIF-1) which is an inhibitor of alpha-MSH release. Compared to control, [3H]DA uptake increased significantly when the synaptosomal fraction of CP was incubated with 0.1 and 1 microM of alpha-MSH and also when the rat was previously injected with alpha-MSH. A simultaneous reduction of endogenous dopamine content was observed. Kinetic studies suggest that the enhanced uptake induced by alpha-MSH 1 microM is the consequence of the rise in Vmax, without changes in the apparent km. The uptake of [3H]DA in hypothalamic (MBH) preparations on the other hand, was not modified by the presence of alpha-MSH. PLG did not have any significant effect on [3H]DA uptake either in the CP or in the MBH. alpha-MSH may act as a modulator of the dopaminergic nigrostriatal system and the results obtained incubating CP synaptosomes in its presence demonstrate a possible direct modulator action by alpha-MSH on the terminal area of the substantia nigra neurons.     

促性腺激素释放激素及多巴胺对斜带石斑鱼生长激素分泌及其mRNA表达的调控

研究斜带石斑鱼生长激素分泌及其mRNA表达的调控规律对于性别分化的控制、临床药物的选择,以及石斑鱼的增养殖等均具有重要的理论意义和实践意义。本文应用静态孵育系统,采用放射免疫测定法和化学发光液相杂交实验,研究GnRH和DA对斜带石斑鱼GH分泌、GHmRNA合成的调控作用。100nmol／LsGnRH作用斜带石斑鱼脑垂体碎片1也4h,明显促进GH的释放和GHmRNA的合成,并具有时间依存性;10nmol／L～1μmol／LsGnRH作用1h能明显促进斜带石斑鱼脑垂体释放GH,促进GHmRNA的合成,表现出明显的剂量效应。100nmol／L、1μmol／LmGnRH作用1h以一定的剂量依存方式促进GH的释放、促进GHmRNA的合成,但mGnRH的效应比相应剂量的sGnRH的作用弱。APO为DA受体的非选择性激动剂,不同剂量APO对斜带石斑鱼脑垂体碎片的作用结果显示,10nmol／L-1μmol／L APO以剂量依存方式促进斜带石斑鱼脑垂体碎片释放GH、促进GHmRNA的合成：1μmol／LAPO作用12h以上明显促进GH的释放和GHmRNA的合成,并随时间的延长而增加。与sGnRH对斜带石斑鱼GH释放、GHmRNA合成的作用相比,APO的作用较弱。本文研究结果证实GnRH和DA能促进斜带石斑鱼脑垂体GH释放和GHmRNA合成。     

Dihydroactinidiolide,a natural product against Aβ25-35 induced toxicity in Neuro2a cells: Synthesis,in silico and in vitro studies

Synthesis of natural products has speeded up drug discovery process by minimizing the time for their purification from natural source. Several diseases like Alzheimer's disease (AD) demand exploring multi targeted drug candidates, and for the first time we report the multi AD target inhibitory potential of synthesized dihydroactinidiolide (DA). Though the activity of DA in several solvent extracts have been proved to possess free radical scavenging, anti bacterial and anti cancer activities, its neuroprotective efficacy has not been evidenced yet. Hence DA was successfully synthesized from β-ionone using facile two-step oxidation method. It showed potent acetylcholinesterase (AChE) inhibition with half maximal inhibitory concentration (IC₅₀) 34.03 nM, which was further supported by molecular docking results showing strong H bonding with some of the active site residues such as GLY117, GLY119 and SER200 of AChE. Further it displayed DPPH and (.NO) scavenging activity with IC₅₀ value 50 nM and metal chelating activity with IC₅₀ >270 nM. Besides, it significantly prevented amyloid β_25-35 self-aggregation and promoted its disaggregation at 270 nM. It did not show cytotoxic effect towards Neuro2a (N2a) cells up to 24 h at 50 and 270 nM while it significantly increased viability of amyloid β_25-35 treated N2a cells through ROS generation at both the concentrations. Cytotoxicity profile of DA against human PBMC was quite impressive. Hemolysis studies also revealed very low hemolysis i.e. minimum 2.35 to maximum 5.61%. It also had suitable ADME properties which proved its druglikeness. The current findings demand for further in vitro and in vivo studies to develop DA as a multi target lead against AD.