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1.
It is noteworthy that in the rat the early postnatal life is marked by an activation of both the corticostimulating function
of the adenohypophysis in neonates of both sexes and of the gonadostimulating function mainly in males. In order to specify
if such neuroendocrine variations are temporally correlated with changes in the hypothalamic metabolism of neurotransmitters,
the hypothalamic metabolism of serotonin (5 HT), norepinephrine (NE), and dopamine (DA) and the hypothalamic content of neuropeptide
Y (NPY) have been investigated in newborn rats of both sexes, delivered at term by cesarean section, as well as changes in
the activity of both the hypothalamo-pituitary adrenal axis (HPA) and the hypothalamo-pituitary gonadal axis (HPG). Experimental
data suggested that 1) in males a rise in hypothalamic metabolism of 5 HT, NE and DA occurs during the first two hours after
delivery, whereas in females, only the metabolism of NE increases. Moreover, the postnatal metabolism of NE was higher in
females than in littermate males; 2) NPY content of the hypothalamus, which was at birth significantly higher in males than
in females, dropped in the former but not in the latter; 3) in newborn males, an early surge of plasma testosterone occurs,
suggesting postnatal activation of the HPG axis; on the other hand, in females, a late and slight increase in plasma estradiol
is observed; 4) in early postnatal life, a sex-independent rise in plasma ACTH and adrenal and plasma corticosterone levels
suggest a comparable activation of the HPA axis in newborns of both sexes. In conclusion, the early postnatal activation of
the corticostimulating function in neonates of both sexes and that of the gonadostimulating function, mainly in males, could
be temporally correlated with a rise in the hypothalamic metabolism of two neurotransmitters, 5 HT and NE, and of NPY content.
According to our data, a sex-dependent metabolsim of neurotransmitters in the hypothalamus is already apparent in early postnatal
life. 相似文献
2.
The population of great hornbills (Buceros bicornis) in the United States is rapidly aging, and captive breeding efforts have not met population managers' expectations for a sustainable captive group. Little is known about the reproductive physiology of these birds. This study reports the first data on the re‐productive endocrinology of the great hornbill. The hormone profiles of the only pair of these birds that hatched a chick in the 1999–2000 breeding season are compared to the profiles of six other pairs of hornbills, from different institutions in the United States, that did not reproduce successfully that season. The study investigates the estradiol, corticosterone, and testosterone profiles of these seven pairs of birds, establishing a base of knowledge from which endocrine data may be used to improve the success of captive breeding programs. The estradiol profiles from this study indicate a difference in hormonal patterns between laying and non‐laying female great hornbills. Egg‐laying females had significantly higher estradiol concentrations during the breeding season than the non‐laying females (P<0.003). Testosterone concentrations of the males were not significantly different between the mates of egg‐laying and non‐egg‐laying females. The corticosterone concentrations tended to be lower in the females that laid eggs vs. the non‐egg‐laying group. The males of the egg‐laying pairs showed a significantly lower (P<0.036) corticosterone concentration than the non‐egg‐laying male pairs. This, combined with the extremely low corticosterone levels (compared to the other birds in the study) of the pair of hornbills that hatched a chick in the 1999–2000 breeding season, suggests that adrenal activity may play a role in the reproductive failure of some captive great hornbills. Zoo Biol 22:135–145, 2003. © 2003 Wiley‐Liss, Inc. 相似文献
3.
肥胖可以增加骨密度、减少骨质疏松的发生。而大多数肥胖者血清瘦素水平升高,并与肥胖的程度呈正相关。研究证实,来源于脂肪组织的瘦素可直接作用于骨细胞和软骨细胞,进而影响其增殖分化。瘦素通过抑制脑5-羟色胺(serotonin,5-HT)的合成、神经肽Y(neuropeptide Y,NPY)的表达等,并经由交感神经系统(sympathetic nervous system,SNS)介导的成骨细胞内p2肾上腺素能受体(B2-adrenergic receptor,Adrl32)信号通路共同调节骨代谢。这些工作为治疗骨质疏松、骨性关节炎等的新策略提供了理论基础。 相似文献
4.
The metabolic and nutritional status of an organism influences multiple behaviors in addition to food intake. When an organism
is hungry, it employs behaviors that help it locate and ingest food while suppressing behaviors that are not associated with
this goal. Alternatively, when an organism is satiated, food-seeking behaviors are repressed so that the animal can direct
itself to other goal-oriented tasks such as reproductive behaviors. Studies in both vertebrate and invertebrate model systems
have revealed that food-deprived and -satiated behaviors are differentially executed and integrated via common molecular signaling
mechanisms. This article discusses cellular and molecular mechanisms for how insulin, neuropeptide Y (NPY), and serotonin
utilize common signaling pathways to integrate feeding and metabolic state with other motivated behaviors. Insulin, NPY, and
serotonin are three of the most well-studied molecules implicated in regulating such behaviors. Overall, insulin signaling
allows an organism to coordinate proper behavioral output with changes in metabolism, NPY activates behaviors required for
locating and ingesting food, and serotonin modulates behaviors performed when an organism is satiated. These three molecules
work to ensure that the proper behaviors are executed in response to the feeding state of an organism.
These authors contributed equally to this work. 相似文献
5.
Nicholas A. Tritos Gabriella Segal‐Lieberman Peter S. Vezeridis Eleftheria Maratos‐Flier 《Obesity (Silver Spring, Md.)》2004,12(4):716-724
Objective: Treatment of male rodents with estradiol (E2) is associated with anorexia and weight loss by poorly understood mechanisms. We examined the role of the orexigenic hypothalamic peptide melanin‐concentrating hormone (MCH) and the appetite‐inhibiting, fat‐derived hormone leptin in mediating E2‐induced anorexia. Research Methods and Procedures: We studied the effect of E2 treatment (implantation of either E2 pellet or matching placebo) in male C57Bl/6J mice, as well as in a lean mouse model (MCH knockout mice) and an obese model (leptin‐deficient ob/ob mice). We also studied the effect of E2 treatment in the context of high‐fat diet. Results: We confirmed E2 dose‐dependent anorexia in male wild type mice fed a normal chow diet. E2 treatment was associated with a significant decrease in body fat, serum leptin levels, and arcuate hypothalamic proopiomelanocortin expression. E2‐implanted mice also showed increased hypothalamic neuropeptide Y and MCH expression. As MCH has been implicated in E2‐induced hypophagia, we performed E2 pellet implantation in MCH knockout mice and observed hypophagia and weight loss, indicating that MCH is not an essential mediator of E2‐induced anorexia. E2‐implanted ob/ob mice also had hypophagia and weight loss, indicating that leptin is not essential for E2‐induced anorexia. High‐fat diet significantly exacerbated the effect of E2 treatment, leading to a 99.6% decrease in food intake at 48 hours and a 30% loss of body weight within 1 week. Discussion: The anorectic effects of E2 were independent of MCH and leptin. Our results suggested that E2 may have effects on nutrient preferences. 相似文献
6.
神经肽Y(NPY)的生理功能研究进展 总被引:11,自引:0,他引:11
神经肽Y(NPY)是机体内的一种重要且保守的神经递质,一般以前体形式存在,释放的有活性的NPY主要通过与其受体结合发挥作用。NPY受体包含了亚型Y1、Y2、Y3、Y4、Y5、Y6、Y7、Y8。Y1和Y2是NPY发挥收缩血管作用的关键受体;Y1、Y2和Y5是NPY调节动物摄食行为的关键受体;Y1、Y2和Y4是NPY调控动物焦虑、沮丧行为的必要受体。着重对NPY与其各种受体结合后如何行使动物的相关生理功能的情况进行了阐述。 相似文献
7.
Ei Terasawa 《Cellular and molecular neurobiology》1995,15(1):141-164
Summary 1. The pulsatile release of luteinizing hormone-releasing hormone (LHRH) is critical for reproductive function. However, the exact mechanism of LHRH pulse generation is unclear. The purpose of this article is to review the current knowledge on LHRH pulse generation and to discuss a series of studies in our laboratory.2. Using push-pull perfusion in the stalk-median eminence of the rhesus monkey several important facts have been revealed. There is evidence indicating that LHRH neurons themselves have endogenous pulse-generating mechanisms but that the pulsatility of LHRH release is also modulated by input from neuropeptide Y (NPY) and norepinephrine (NE) neurons. The release of NPY and NE is pulsatile, with their pulses preceding or occurring simultaneously with LHRH pulses, and the neuroligands NPY and NE and their agonists stimulate LHRH pulses, while the antagonists of the ligands suppress LHRH pulses.3. The pulsatile release of LHRH increases during the estrogen-induced LH surge as well as the progesterone-induced LH surge. These increases are partly due to the stimulatory effects of estrogen and progesterone on NPY neurons.4. An increase in pulsatile LHRH release occurs at the onset of puberty. This pubertal increase in LHRH release appears to be due to the removal of tonic inhibition from aminobutyric acid (GABA) neurons and a subsequent increase in the inputs of NPY and NE neurons to LHRH neurons.5. There are indications that additional neuromodulators are involved in the control of the LHRH pulse generation and that glia may play a role in coordinating pulses of the release of LHRH and neuromodulators.6. It is concluded that the mechanism generating LHRH pulses appears to comprise highly complex cellular elements in the hypothalamus. The study of neuronal and nonneuronal elements of LHRH pulse generation may serve as a model to study the oscillatory behavior of neurosecretion. 相似文献
8.
YVES-MARIE PAULET ANNE DONVAL FARIDA BEKHADRA 《Invertebrate reproduction & development.》2013,57(2-3):89-94
Summary The distribution of serotonin-like immunoreactivity was studied in the central nervous system and the gonad of Pecten maximus. Cerebral and pedal ganglia contain a well developed serotonin-immunoreactive neuronal subpopulation, whereas positive neurons are scarce in the visceral ganglion. The distribution pattern of immunoreactive elements in the gonad indicate that serotonin is involved in peripheral neurotransmission of this organ. Seasonal variations of monoamines (serotonin, dopamine and noradrenaline) have been investigated in the nervous system using HPLC. Lower concentrations of serotonin are observed during winter in the central nervous system; dopamine levels of the visceral ganglion are correlated to gonadal growth. 相似文献
9.
10.
Vincent Fournet Gaetan de Lavilléon Annie Schweitzer Bruno Giros Annie Andrieux Marie‐Pascale Martres 《Journal of neurochemistry》2012,123(6):982-996
Recent evidence underlines the crucial role of neuronal cytoskeleton in the pathophysiology of psychiatric diseases. In this line, the deletion of STOP/MAP6 (Stable Tubule Only Polypeptide), a microtubule‐stabilizing protein, triggers various neurotransmission and behavioral defects, suggesting that STOP knockout (KO) mice could be a relevant experimental model for schizoaffective symptoms. To establish the predictive validity of such a mouse line, in which the brain serotonergic tone is dramatically imbalanced, the effects of a chronic fluoxetine treatment on the mood status of STOP KO mice were characterized. Moreover, we determined the impact, on mood, of a chronic treatment by epothilone D, a taxol‐like microtubule‐stabilizing compound that has previously been shown to improve the synaptic plasticity deficits of STOP KO mice. We demonstrated that chronic fluoxetine was either antidepressive and anxiolytic, or pro‐depressive and anxiogenic, depending on the paradigm used to test treated mutant mice. Furthermore, control‐treated STOP KO mice exhibited paradoxical behaviors, compared with their clear‐cut basal mood status. Paradoxical fluoxetine effects and control‐treated STOP KO behaviors could be because of their hyper‐reactivity to acute and chronic stress. Interestingly, both epothilone D and fluoxetine chronic treatments improved the short‐term memory of STOP KO mice. Such treatments did not affect the serotonin and norepinephrine transporter densities in cerebral areas of mice. Altogether, these data demonstrated that STOP KO mice could represent a useful model to study the relationship between cytoskeleton, mood, and stress, and to test innovative mood treatments, such as microtubule‐stabilizing compounds. 相似文献
11.
Hope SI Schmipp J Rossi AH Bianciotti LG Vatta MS 《Neurochemistry international》2008,53(6-8):207-213
We previously reported that endothelin-1 and endothelin-3 modulate norepinephrine neuronal release and tyrosine hydroxylase activity and expression in the hypothalamus. In the present study we sought to establish the role of endothelin-1 and -3 in the regulation of norepinephrine uptake in the anterior and posterior hypothalamus. Results showed that in the anterior hypothalamus endothelin-3 increased neuronal norepinephrine uptake whereas endothelin-1 decreased it. Conversely, in the posterior hypothalamic region both endothelins diminished the neuronal uptake of the amine. Endothelins response was concentration dependent and maintained at all studied times. Endothelins also modified the kinetic and internalization of the NE neuronal transporter. In the anterior hypothalamic region endothelin-3 increased the Vmax and the Bmax whereas endothelin-1 decreased them. However, in the posterior hypothalamic region both endothelins diminished the Vmax as well as Bmax. Neither endothelin-1 nor endothelin-3 modified neuronal norepinephrine transporter Kd in the studied hypothalamic regions. These findings support that in the posterior hypothalamic region both endothelins diminished neuronal norepinephrine transporter activity by reducing the amine transporter expression on the plasmatic membrane. Conversely, in the anterior hypothalamic region endothelin-3 enhanced neuronal norepinephrine transporter activity by increasing the expression of the transporter on the presynaptic membrane, whereas endothelin-1 induced the opposite effect. Present results permit us to conclude that both endothelins play an important role in the regulation of norepinephrine neurotransmission at the presynaptic nerve endings in the hypothalamus. 相似文献
12.
本实验采用离体孵育脑薄片技术,初步探讨了皮质酮快速抑制大鼠下丘脑薄片释放精氨酸加压素(AVP)的机制。结果表明:(1)放线菌素D(基因转录抑制剂)、嘌呤霉素(蛋白质合成抑制剂)和秋水仙碱(轴浆运输阻滞剂)均不影响皮质酮的快速抑制效应;(2)提高孵育液Ca ̄(2+)浓度,AVP释放增加,皮质酮的快速抑制效应明显增强;反之,孵育液中无Ca ̄(2+)则AVP释放减少,皮质酮的快速抑制效应也减弱;(3)新霉素(抑制细胞膜磷酸肌醇水解)使皮质酮的快速抑制效应增强。(4)氨茶碱(磷酸二酯酶抑制剂)不影响皮质酮的快速抑制效应。提示,皮质酮对大鼠下丘脑薄片释放AVP的快速抑制效应没有通过传统的基因组机制,而由非基因纽机制介导,推测可能是影响Ca ̄(2+)的跨细胞膜流动或/和细胞内Ca ̄(2+)释放的结果。 相似文献
13.
目的:研究低氧对雄性大鼠性腺及相关激素水平的影响。方法:分别检测3km、5km及杭州海拔水平雄性大鼠睾丸和附睾指数、血浆皮质酮和睾酮水平。结果:3km组体重、睾酮含量均显著下降,睾丸指数、血浆皮质酮显著上升;5km组体重、附睾指数和睾酮含量均显著下降,皮质酮含量显著上升。结论:慢性低氧能显著影响雄性成年大鼠性腺及血浆睾酮水平,该结果显示哺乳动物在慢性低氧条件下生殖内分泌功能呈现抑制状态。 相似文献
14.
Alvaro AR Martins J Araújo IM Rosmaninho-Salgado J Ambrósio AF Cavadas C 《Journal of neurochemistry》2008,105(6):2501-2510
Neuropeptide Y (NPY) is a 36 amino acid peptide widely present in the CNS, including the retina. Previous studies have demonstrated that NPY promotes cell proliferation of rat post-natal hippocampal and olfactory epithelium precursor cells. The aim of this work was to investigate the role of NPY on cell proliferation of rat retinal neural cells. For this purpose, primary retinal cell cultures expressing NPY, and NPY Y1 , Y2 , Y4 and Y5 receptors [Álvaro et al. , (2007) Neurochem. Int., 50, 757] were used. NPY (10–1000 nM) stimulated cell proliferation through the activation of NPY Y1 , Y2 and Y5 receptors. NPY also increased the number of proliferating neuronal progenitor cells (BrdU+ /nestin+ cells). The intracellular mechanisms coupled to NPY receptors activation that mediate the increase in cell proliferation were also investigated. The stimulatory effect of NPY on cell proliferation was reduced by l -nitroarginine-methyl-esther ( l -NAME; 500 μM), a nitric oxide synthase inhibitor, 1H-[1,2,4]oxadiazolo-[4, 3-a]quinoxalin-1-one (ODQ; 20 μM), a soluble guanylyl cyclase inhibitor or U0126 (1 μM), an inhibitor of the extracellular signal-regulated kinase 1/2 (ERK 1/2). In conclusion, NPY stimulates retinal neural cell proliferation, and this effect is mediated through nitric oxide–cyclic GMP and ERK 1/2 pathways. 相似文献
15.
Eva C Mele P Collura D Nai A Pisu MG Serra M Biggio G 《Journal of neurochemistry》2008,104(4):1043-1054
Previous studies have shown that GABAergic neuroactive steroids increase Y1 receptor (Y1 R) gene expression in the amygdala of Y 1 R / LacZ transgenic mice, harbouring the murine Y1 R gene promoter linked to a LacZ reporter gene. As ethanol is known to increase GABAergic neuroactive steroids, we investigated the relationship between fluctuations in the brain content of neuroactive steroids induced by chronic voluntary ethanol consumption or ethanol discontinuation and both the level of neuropeptide Y (NPY) immunoreactivity and Y1 R gene expression in the amygdala of Y 1 R / LacZ transgenic mice. Ethanol discontinuation (48 h) after voluntary consumption of consecutive solutions of 3%, 6%, 10% and 20% (v/v) ethanol over 4 weeks produced an anxiety-like behaviour as measured by elevated plus maze. Voluntary ethanol intake increased the cerebrocortical concentration of the progesterone metabolite 3α-hydroxy-5α-pregnan-20-one (3α,5α-TH PROG) that returned to control level 48 h after discontinuation of ethanol intake. Ethanol discontinuation significantly decreased NPY immunoreactivity and concomitantly increased Y 1 R / LacZ transgene expression in the amygdala, whereas chronic ethanol intake failed to affect these parameters. The 5α-reductase inhibitor finasteride prevented both the increase in the cerebrocortical concentration of 3α,5α-TH PROG apparent after 4 weeks of ethanol intake and the changes in NPY immunoreactivity and transgene expression induced by ethanol discontinuation. Data suggest that 3α,5α-TH PROG plays an important role in the changes in NPY–Y1 R signalling in the amygdala during ethanol discontinuation. 相似文献
16.
Y2受体亚型是早期发现的NPY的两种主要受体亚型之一,参与NPY所介导的多种生理和病理功能.为了制备Y2受体抗体和开展Y2受体的定位研究,用RT-PCR方法从大鼠海马的总RNA扩增NPY的Y2受体全长基因,接着PCR扩增Y2受体的C端片段,克隆入表达载体中,建立了重组NPY Y2受体C端肽的表达菌株,并对表达产物进行纯化. 相似文献
17.
P.B. Applewhite 《Phytochemistry》1973,12(1):191-192
18.
Meddle SL Romero LM Astheimer LB Buttemer WA Moore IT Wingfield JC 《Hormones and behavior》2002,42(2):212-221
The breeding season is very brief for arctic-breeding passerines, and any interruptions of parental care by aggressive interactions over territory may reduce reproductive success. We tested both the testosterone insensitivity and corticosterone insensitivity hypotheses in the arctic-breeding Gambel's white-crowned sparrow, Zonotrichia leucophrys gambelii. Additionally, we tested whether simulated territorial intrusions (STIs), known to stimulate increases in luteinizing hormone (LH) and testosterone (T) in mid-latitude breeding Z. l. pugetensis, would also be effective in either the early or late phases of the brief breeding season of Z. l. gambelii. Plasma levels of T and LH were high early in the breeding season and declined as egg laying began. Exposure of free-living males to 10 min of STI significantly increased LH but not T secretion. Nonetheless, the pituitary-gonadal axis is sensitive as jugular injection of gonadotrophin-releasing hormone increased plasma T at 10 min relative to saline-challenged controls. T implants failed to increase territorial aggression following STI during incubation. These data are consistent with the T insensitivity hypothesis and contrast sharply with the response of the southerly breeding subspecies, Z. l. pugetensis, in which the territorial response to T administration is retained throughout its relatively long breeding season. However, corticosterone implants during the incubation period decreased territorial aggression during STI. This responsiveness to corticosterone is not consistent with the corticosterone insensitivity hypothesis of stress modulation. Z. l. gambelii retain sensitivity to corticosterone levels that may occur naturally in response to environmental perturbations resulting in suppression of territorial behavior. 相似文献
19.
George A. Bray Donna H. Ryan Douglas Gordon Sylvia Heidingsfelder Frederick Cerise Krause Wilson 《Obesity (Silver Spring, Md.)》1996,4(3):263-270
Sibutramine is a β-phenethylamine which blocks reuptake of norepinephrine and serotonin. In this clinical study, a group of 173 patients were randomized to treatment with sibutramine at doses of 1, 5, 10, 15, 20 or 30 mg/d and were compared with placebo in a 24-week double-blind trial. There was a dose-dependent reduction in body weight, with doses of 10, 15, 20 and 30 mg being significantly greater than placebo. Weight loss was still continuing in the highest three doses at the end of the study. When drugs were discontinued patients regained weight, as expected. Side effects were generally mild and were most evident in the group treated with the highest dose. These studies suggest that sibutramine may be a valuable new drug for treatment of obesity. 相似文献
20.
5—羟色胺对大鼠下丘脑脑薄片室旁核神经元自发电活动的作用 总被引:1,自引:1,他引:1
在20个下丘脑脑片上,用玻璃微电极细胞外记录了46个室旁核神经元的自发放电单位,观察了5-羟色胺对它们的作用。当薄片用含5-羟色胺(10~(-6)mol/L)的人工脑脊液灌流后,有16个单位放电频率明显增加,反应的潜伏期为1.21±1.21 min。这种反应可被5-羟色胺的阻断剂噻庚啶所阻断。3个单位放电频率明显减少,27个单位无明显反应。实验结果表明约1/3的下丘脑室旁核神经元能被5-羟色胺所激活。 相似文献