Advances in biochemical psychopharmacology最新文献

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Selective expression of the mRNA encoding the short isoform of the gamma 2 GABA-A receptor subunit in rat pituitary cells. 编码γ - 2 GABA-A受体亚基短亚型mRNA在大鼠垂体细胞中的选择性表达。
A Valerio, P F Spano, M Memo
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引用次数: 0
Neurosteroids and GABAA receptor function. 神经类固醇和GABAA受体功能。
R H Purdy, P H Moore, A L Morrow, S M Paul
{"title":"Neurosteroids and GABAA receptor function.","authors":"R H Purdy, P H Moore, A L Morrow, S M Paul","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":7274,"journal":{"name":"Advances in biochemical psychopharmacology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1992-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12527621","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The involvement of the benzodiazepine receptor in hepatic encephalopathy: evidence for the presence of a benzodiazepine receptor ligand. 苯二氮卓受体在肝性脑病中的作用:苯二氮卓受体配体存在的证据。
A S Basile, N L Ostrowski, S H Gammal, E A Jones, P Skolnick
{"title":"The involvement of the benzodiazepine receptor in hepatic encephalopathy: evidence for the presence of a benzodiazepine receptor ligand.","authors":"A S Basile,&nbsp;N L Ostrowski,&nbsp;S H Gammal,&nbsp;E A Jones,&nbsp;P Skolnick","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>The involvement of GABAergic systems in the pathogenesis of HE was supported by electrophysiologic studies of single Purkinje neurons from rabbits with HE which demonstrated the hypersensitivity of these neurons to depression by GABA and BZ receptor agonists. In contrast, these neurons were excited by BZ receptor antagonists. At concentrations which had no effect on neuronal activity, BZ receptor antagonists also reversed the hypersensitivity of HE neurons to depression by muscimol. This combination of neuronal responses is consistent with an increase in the concentration or availability of a ligand for the BZ receptor with agonist properties in the brains of rabbits with HE. Subsequent neurochemical studies support these electrophysiologic observations. Autoradiographic techniques indicated the presence of a reversible inhibitor of [3H]Ro 15-1788 and [3H]flunitrazepam binding to the cerebral and cerebellar cortices of rabbits with HE. The ability of this substance to inhibit [3H]flunitrazepam binding to HE rabbit brain sections was further enhanced in the presence of NaCl and GABA. The autoradiographic studies suggested that the density and affinity of the components of the GABA-BZ receptor complex are unaltered in this animal model of HE. This inference is fully supported by the subsequent studies of radioligand binding to well-washed membrane preparations. Finally, extracts of HE rabbit brains yielded a family of substances with the properties of BZ receptor agonists. These substances may include, but are not limited to, diazepam, oxazepam and desmethyldiazepam, but do not include substances commonly elevated in the plasma and CSF of patients with HE4. The positive identification of these substances awaits confirmation by mass-spectroscopic analysis. However, the precedent for the presence of a family of benzodiazepines in animals that were not administered these drugs has been set. The origin of these substances is a matter of ongoing research. Several studies have shown the presence of benzodiazepines in plant and animal materials. It is possible that these \"endogenous\" benzodiazepines are the result of contamination of the food chain. A normally functioning liver would capture and metabolize these compounds after their absorption from the gut. This function of the liver would be impaired in liver failure, thus allowing sufficient levels of BZ receptor agonists to accumulate in the CNS, contributing to the pathogenesis of HE. However, studies by DeBlas and coworkers have reported that 1,4 benzodiazepines are present in human brains preserved prior to the commercial use of these compounds. Further, they have found benzodiazepines in cell lines cultured without potential exogenous sources of benzodiazepines.(ABSTRACT TRUNCATED AT 400 WORDS)</p>","PeriodicalId":7274,"journal":{"name":"Advances in biochemical psychopharmacology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1990-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"13122008","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Chronic benzodiazepine administration: effects in vivo and in vitro. 慢性苯二氮卓类药物的体内和体外作用。
L G Miller, D J Greenblatt, F Lopez, A Schatzki, J Heller, M Lumpkin, R I Shader
{"title":"Chronic benzodiazepine administration: effects in vivo and in vitro.","authors":"L G Miller,&nbsp;D J Greenblatt,&nbsp;F Lopez,&nbsp;A Schatzki,&nbsp;J Heller,&nbsp;M Lumpkin,&nbsp;R I Shader","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>Chronic benzodiazepine administration is associated with neurochemical alterations in the GABAergic system, as determined in a variety of animal models and tissue culture systems. In animals, effects of chronic benzodiazepine agonists on receptor binding are uncertain, but several studies indicate a decrease in GABA-dependent chloride uptake. In contrast, limited data indicate that chloride uptake is increased after chronic antagonist administration, and results of inverse agonist administration are uncertain. Most animal studies are limited by lack of attention to drug choice and to pharmacokinetic variables, and by failure to determined delivered drug concentrations. More limited data in tissue culture systems are conflicting with regard to effects on benzodiazepine binding, but recent studies indicate that GABA-dependent chloride uptake may be decreased after chronic agonist exposure, and increased after chronic antagonist and inverse agonist administration. Data from these systems may complement results obtained in intact animals, and cultures may allow more detailed examination of the kinetics and specificity of drug effects.</p>","PeriodicalId":7274,"journal":{"name":"Advances in biochemical psychopharmacology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1990-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"13139697","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
"Spare receptors" and "partial agonists"--romantic terms to explain a pharmacology deriving from the structural diversity of GABAA receptors. “备用受体”和“部分激动剂”——浪漫的术语来解释从GABAA受体结构多样性衍生的药理学。
E Costa
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引用次数: 0
GABA and benzodiazepine receptor subtypes. Molecular biology, pharmacology, and clinical aspects. Proceedings of the 6th Capo Boi Conference on Neuroscience. Villasimius, Italy, June 1989. GABA和苯二氮卓受体亚型。分子生物学、药理学和临床方面。第六届波伊角神经科学会议论文集。Villasimius,意大利,1989年6月。
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引用次数: 0
Chronic administration of negative modulators produces chemical kindling and GABAA receptor down-regulation. 长期服用负调剂会产生化学点燃和GABAA受体下调。
M G Corda, O Giorgi, M Orlandi, B Longoni, G Biggio
{"title":"Chronic administration of negative modulators produces chemical kindling and GABAA receptor down-regulation.","authors":"M G Corda,&nbsp;O Giorgi,&nbsp;M Orlandi,&nbsp;B Longoni,&nbsp;G Biggio","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":7274,"journal":{"name":"Advances in biochemical psychopharmacology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1990-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"13122006","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Hepatic encephalopathy: neurochemical mechanisms and new treatments. 肝性脑病:神经化学机制和新的治疗方法。
M Baraldi, P Zanoli, M L Zeneroli
{"title":"Hepatic encephalopathy: neurochemical mechanisms and new treatments.","authors":"M Baraldi,&nbsp;P Zanoli,&nbsp;M L Zeneroli","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":7274,"journal":{"name":"Advances in biochemical psychopharmacology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1990-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"13122007","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
"Ex vivo" binding of 35S-TBPS as a tool to study the pharmacology of GABAA receptors. 体外结合35S-TBPS作为研究GABAA受体药理学的工具。
A Concas, E Sanna, M Serra, M P Mascia, V Santoro, G Biggio
{"title":"\"Ex vivo\" binding of 35S-TBPS as a tool to study the pharmacology of GABAA receptors.","authors":"A Concas,&nbsp;E Sanna,&nbsp;M Serra,&nbsp;M P Mascia,&nbsp;V Santoro,&nbsp;G Biggio","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":7274,"journal":{"name":"Advances in biochemical psychopharmacology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1990-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"13122013","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Benzodiazepine binding inhibitory activity (B.B.I.A.) in human plasma. 人血浆中苯二氮卓类药物结合抑制活性(b.b.i.a)。
D Marazziti, S Michelini, C Martini, G Giannaccini, G B Cassano, A Lucacchini
{"title":"Benzodiazepine binding inhibitory activity (B.B.I.A.) in human plasma.","authors":"D Marazziti,&nbsp;S Michelini,&nbsp;C Martini,&nbsp;G Giannaccini,&nbsp;G B Cassano,&nbsp;A Lucacchini","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":7274,"journal":{"name":"Advances in biochemical psychopharmacology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1990-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"13122009","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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