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Effects of Activation and Blockade of Serotonin 5-HT1A Receptors on the Immune Response in Rats Selected for Different Levels of Aggressiveness
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作者 Elizaveta Alperina Elena Zhukova +2 位作者 Galina Idova Rimma Kozhemyakina Margarita Cheido 《Pharmacology & Pharmacy》 2015年第9期451-459,共9页
The present study examines the effects of serotonin (5-HT) 1A receptor ligands on humoral im-mune response in two rat lines selected for over 75 generations for the enhancement or elimination of aggression. Activation... The present study examines the effects of serotonin (5-HT) 1A receptor ligands on humoral im-mune response in two rat lines selected for over 75 generations for the enhancement or elimination of aggression. Activation of presynaptic 5-HT1A receptors with a low dose of the selective 5-HT1A receptor agonist 8-OH-DPAT (0.1 mg/kg) or the blockade of postsynaptic 5-HT1A receptors with the antagonist WAY-100635 (1.0 mg/kg) did not affect the numbers of IgM-antibody forming cells (IgM-AFC) in the spleen of highly aggressive rats, which were characterized by higher immune responsiveness compared to nonaggressive line. On the other hand, the same doses of 8-OH-DPAT and WAY-100635, as well as a higher dose of 8-OH-DPAT (1.0 mg/kg), which is known to activate postsynaptic 5-HT1A receptors, produce immunostimulation in nonaggressive rats. However, only the highest dose of 8-OH-DPAT (5.0 mg/kg) was able to cause immunosuppression in nonaggressive rats that was mainly dependent on stimulation of postsynaptic 5-HT1A receptors. In contrast to nonaggressive rats, the dose of 1.0 mg/kg 8-OH-DPAT was sufficient to produce a decrease in the numbers of IgM-AFC in highly aggressive rats. Thus, pharmacological activation of pre- and postsynaptic 5-HT1A receptors, as well as the blockade of postsynaptic 5-HT1A receptors, produced different effects on the immune response in two lines of rats selected for high level of aggression or its absence. These data may have implications for more efficient treatments of a number of mental disorders associated with abnormal aggression. 展开更多
关键词 Aggressive Behavior serotonin Pre- and POSTSYNAPTIC 5-ht1a receptors 8-OH-DPAT WAY-100635 IgM-Immune Response
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^(99)Tc^m标记5-HT_(1A)脑受体显像剂的研制及其生物分布 被引量:3
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作者 刘飞 贺佑丰 +1 位作者 罗志福 刘英妹 《同位素》 CAS 2001年第3期129-135,共7页
为了寻找 99Tcm 标记中枢神经系统 5 - HT1A协同受体显像药物 ,合成了单齿受体配基 1- (2 -甲氧基苯基 ) - 4 - (2 -巯基乙基 )哌嗪 (简称 MPMEP)、三齿配体 N,N-二 (2 -巯基乙基 ) - N',N'-二乙基乙二胺 (简称 BMPDEEDA)和 N,N... 为了寻找 99Tcm 标记中枢神经系统 5 - HT1A协同受体显像药物 ,合成了单齿受体配基 1- (2 -甲氧基苯基 ) - 4 - (2 -巯基乙基 )哌嗪 (简称 MPMEP)、三齿配体 N,N-二 (2 -巯基乙基 ) - N',N'-二乙基乙二胺 (简称 BMPDEEDA)和 N,N-二 (2 -巯基乙基 )卞胺 (简称 BMPBA) ,其结构经 IR、NMR及元素分析表征 ;以“3+ 1”混合配体进行了 99Tcm标记 ,并确定了标记反应的最佳条件 :p H=6 .0~ 7.0 ,6 0~70℃下 ,反应 2 0~ 30 min,经 CH2 Cl2 萃取脂溶性部分后 ,99Tcm O(MPMEP) (BMPDEEDA)和 99Tcm O(MPMEP) (BMPBA)的标记率分别达到 95 %和 90 %以上。采用 HPL C对标记产物进行了分离和纯化 ,纯化后的标记物放化纯度均 >98%。小鼠体内的生物分布结果表明 99Tcm O(MPMEP)(BMPDEEDA)和 99Tcm O(MPMEP) (BMPBA)配合物可以通过血脑屏障 ,在脑中有一定的摄取和滞留 ;99Tcm O(MPMEP) (BMPBA)在血液中清除较快 ,静脉注射后 2、30、6 0 min时 ,脑与血摄取比分别为 0 .31、0 .33、0 .32 。 展开更多
关键词 脑受体显像剂 5-ht1a ^99TC^M “3+1”混合配体标记 生物分布 锝99 5-羟色胺 放射性药物 神经系统疾病 病理
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一种^(99)Tc^m标记的5-HT_(1A)受体显像剂的合成与标记
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作者 蒋泉福 吴春英 +4 位作者 陆春雄 陈正平 王颂佩 张同兴 李晓敏 《同位素》 CAS 北大核心 2006年第3期150-153,共4页
合成了一种99Tcm标记的5-HT1A受体显像剂。该显像剂先由二硫二氮与6-溴己酰氯结合,再与2-(1-哌嗪)苯甲醚结合,经还原、脱保护反应得到标记前体,再对前体进行99Tcm标记。标记率达90%以上,薄层层析测得标记物放化纯度大于95%。
关键词 ^99TC^M标记 5-ht1a受体显像剂 合成
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1-[2-(2-Methoxyphenylthio) benzyl]-4-arylpiperazines derivatives:Synthesis and evaluation for dual 5-HT_(1A)/SSRI activities 被引量:1
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作者 Xin Wang Dong Zhi Liu Ai Jun Li 《Chinese Chemical Letters》 SCIE CAS CSCD 2008年第1期37-39,共3页
A series of 1-[2-(2-methoxyphenylthio) benzyl]-4-arylpiperazines derivatives was designed and synthesized based on 5-HT1A/ SSRI drugs design strategies. The synthesized compounds were evaluated for their dual 5-HT1A... A series of 1-[2-(2-methoxyphenylthio) benzyl]-4-arylpiperazines derivatives was designed and synthesized based on 5-HT1A/ SSRI drugs design strategies. The synthesized compounds were evaluated for their dual 5-HT1A/5-HTT activities. 2007 Ai Jun Li. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved. 展开更多
关键词 Antidepressants 5-ht1a/5-htT serotonin transporter 5-ht1a receptor Diphenylsulfide
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1-(N-(2-(2-Methoxyphenylthio)benzyl)-N-methylamino-3-aryloxypropan-2-ols:Synthesis and evaluation for dual 5-HT_(1A)/SSRI activities 被引量:1
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作者 Xin Wang Dong Zhi Liu Ai Jun Li 《Chinese Chemical Letters》 SCIE CAS CSCD 2008年第1期40-42,共3页
A series of 1-(N-(2-(2-methoxyphenylthio)benzyl)-N-methylamino-3-aryloxypropan-2-ols derivatives were designed and synthesized based on 5-HT1A/SSRI drugs design strategies. The synthesized compounds were evaluate... A series of 1-(N-(2-(2-methoxyphenylthio)benzyl)-N-methylamino-3-aryloxypropan-2-ols derivatives were designed and synthesized based on 5-HT1A/SSRI drugs design strategies. The synthesized compounds were evaluated for their dual 5-HT1A/ 5-HTT activities. 2007 Ai Jun Li. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved. 展开更多
关键词 5-ht1a/SSRI serotonin transporter 5-ht1a receptor Diphenylsulfide
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Molecular signaling of 5-HT<sub>1A</sub>and presence of serotonergic cells in the fetal cerebral cortex
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作者 Alfonso B. M. de Oca Gabriel M. Gutiérrez Jorge H. Rodríguez 《World Journal of Neuroscience》 2013年第2期76-82,共7页
Early appearance of the serotonergic system in the fetal brain and the various effects of serotonin (5-HT) on brain morphogenesis, have given support to a neurotrophic role of serotonin. This function of serotonin is ... Early appearance of the serotonergic system in the fetal brain and the various effects of serotonin (5-HT) on brain morphogenesis, have given support to a neurotrophic role of serotonin. This function of serotonin is accomplished through a system of serotonin nerve terminals in the target regions that involves various 5-HT receptors. In visual, auditory and somatosensory cortex an early and intense serotonergic innervation is particularly important. The neuronal somata of these terminals are normally located in the mesencephalon and they have not been observed in the maturing cerebral cortex, neither in the adult brain. By using immunolabeling techniques, fluorescence and confocal microscopy, we observe the presence of both, 5-HT terminals and 5-HT cells in mesencephalon (Me, E17) and in the neopallium (Np, E13-E16) cocultures. Cells immunopositive to 5-HT and to tryptophan-5-hydroxilase are also observed in the Np on day 12 of culture. These results concerning the unexpected presence of serotonergic cells in the fetal cerebral cortex are interesting and may be of importance in corticogenesis. As it happens with other elements of the serotonergic system, the presence of these phenotypically serotonergic cells in the early cerebral cortex may be transitory and probably supporting cortex maturation processes. The molecular signaling path of the 5-HT1A receptor has also been identified. 展开更多
关键词 SEROTONERGIC System serotonin receptor 5-ht1a Molecular Signaling Paths
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新靶点抗精神病药SEP-363856研究进展 被引量:2
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作者 张月 苏允爱 司天梅 《中华精神科杂志》 CAS CSCD 北大核心 2021年第3期224-228,共5页
精神分裂症是一种慢性高致残性精神障碍,其病因和病理机制复杂。既往抗精神病药主要通过作用于多巴胺2型受体发挥疗效,对阴性症状和认知损害症状的疗效欠佳且出现较多的不良反应,严重影响患者的治疗依从性和功能康复。因此,作用于新靶... 精神分裂症是一种慢性高致残性精神障碍,其病因和病理机制复杂。既往抗精神病药主要通过作用于多巴胺2型受体发挥疗效,对阴性症状和认知损害症状的疗效欠佳且出现较多的不良反应,严重影响患者的治疗依从性和功能康复。因此,作用于新靶点的抗精神病药的研发显得尤为迫切。SEP-363856是基于表型筛选策略发现的一种不与多巴胺2型受体结合的独特抗精神病药,临床前研究数据表明,SEP-363856的疗效可能与激活痕量胺相关受体1和5-羟色胺1A受体有关,该药的发现有望为精神分裂症患者带来新的治疗选择。本文中简要介绍了SEP-363856的研发历程,包括临床前研究结果及最新的临床试验数据,便于读者了解这一新型抗精神病药。 展开更多
关键词 抗精神病药 受体 多巴胺 受体 血清素 5-ht1a SEP-363856 痕量胺相关受体1
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Current developments in pharmacological therapeutics for chronic constipation 被引量:24
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作者 Chunhuan Jiang Qinglong Xu +1 位作者 Xiaoan Wen Hongbin Sun 《Acta Pharmaceutica Sinica B》 SCIE CAS CSCD 2015年第4期300-309,共10页
Chronic constipation is a common gastrointestinal disease severely affecting the patient's quality of life. The traditional treatment of constipation is the use of laxatives. Recently, several new drugs including ... Chronic constipation is a common gastrointestinal disease severely affecting the patient's quality of life. The traditional treatment of constipation is the use of laxatives. Recently, several new drugs including lubiprostone, linaclotide and prucalopride have been approved for treatment of chronic constipation. However, a significant unmet medical need still remains, particularly among those patients achieving poor results by current therapies. The 5-EF1'1 receptor modulators velusetrag and naronapride, the guanylate cy-clase C agonist plecanatide and die deal bile acid transporter inhibitor elobixibat are recognized as the most promising drugs under investigation. Herein, we give a comprehensive review on the pharmacological therapeutics for the treatment of chronic constipation, with the purpose of reflecting the drug development trends in this field. (C) 2015 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.orgicenses/by-ne-rid/4.0/). 展开更多
关键词 Chronic constipation Prokinetic agent 5-ht1 receptor Prosecretory agent
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Clinical Research on Alzheimer's Disease: Progress and Perspectives 被引量:34
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作者 Bin-Lu Sun Wei-Wei Li +7 位作者 Chi Zhu Wang-Sheng Jin Fan Zeng Yu-Hui Liu Xian-Le Bu Jie Zhu Xiu-Qing Yao Yan-Jiang Wang 《Neuroscience Bulletin》 SCIE CAS CSCD 2018年第6期1111-1118,共8页
Alzheimer’s disease(AD), the most common type of dementia, is becoming a major challenge for global health and social care. However, the current understanding of AD pathogenesis is limited, and no early diagnosis and... Alzheimer’s disease(AD), the most common type of dementia, is becoming a major challenge for global health and social care. However, the current understanding of AD pathogenesis is limited, and no early diagnosis and disease-modifying therapy are currently available. During the past year, significant progress has been made in clinical research on the diagnosis, prevention, and treatment of AD.In this review, we summarize the latest achievements,including diagnostic biomarkers, polygenic hazard score,amyloid and tau PET imaging, clinical trials targeting amyloid-beta(Ab), tau, and neurotransmitters, early intervention, and primary prevention and systemic intervention approaches, and provide novel perspectives for further efforts to understand and cure the disease. 展开更多
关键词 Alzheimer's disease AMYLOID-BETA TAU IMMUNOTHERAPY BACE1 inhibitor 5-ht6 receptor antagonist Primary prevention Positron emission tomographic imaging BIOMARKER
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