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1.
Life Sci ; 64(6-7): 535-9, 1999.
Artigo em Inglês | MEDLINE | ID: mdl-10069520

RESUMO

As a decrease in cholinergic neurons has been observed in Alzheimer's Disease (AD), therapeutic approaches to AD include inhibition of acetylcholinesterase to increase acetylcholine levels. Evidence suggests that acetylcholine release in the CNS is modulated by negative feedback via presynaptic M2 receptors, blockade of which should provide another means of increasing acetylcholine release. Structure-activity studies of [4-(phenylsulfonyl)phenyl]methylpiperazines led to the synthesis of 4-cyclohexyl-alpha-[4-[[4-methoxyphenyl]sulfinyl]-phenyl]-1-piperazin eacetonitrile. This compound, SCH 57790, binds to cloned human M2 receptors expressed in CHO cells with an affinity of 2.78 nM; the affinity at M1 receptors is 40-fold lower. SCH 57790 is an antagonist at M2 receptors expressed in CHO cells, as the compound blocks the inhibition of adenylyl cyclase activity mediated by the muscarinic agonist oxotremorine. This compound should be useful in assessing the potential of M2 receptor blockade for enhancement of cognition.


Assuntos
Antagonistas Muscarínicos/farmacologia , Piperazinas/farmacologia , Receptores Muscarínicos/fisiologia , Acetilcolina/metabolismo , Adenilil Ciclases/metabolismo , Doença de Alzheimer/tratamento farmacológico , Animais , Sítios de Ligação , Células CHO , Colforsina/antagonistas & inibidores , Colforsina/farmacologia , Cricetinae , AMP Cíclico/metabolismo , Humanos , Agonistas Muscarínicos/farmacologia , Antagonistas Muscarínicos/química , Antagonistas Muscarínicos/metabolismo , Antagonistas Muscarínicos/uso terapêutico , Oxotremorina/farmacologia , Piperazinas/química , Piperazinas/metabolismo , Quinuclidinil Benzilato/metabolismo , Receptor Muscarínico M2 , Receptores Muscarínicos/metabolismo , Transfecção
2.
Am Heart J ; 124(4): 1026-30, 1992 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-1388323

RESUMO

This report is from a 10-year cohort study of community-dwelling elderly men and women. Mean age at the time of entry into the study was 79 years. Annual chest x-ray studies were performed, and data are presented regarding prevalence, incidence, and prognosis of cardiomegaly. Cardiomegaly was defined as a transverse diameter of the cardiac silhouette greater than or equal to 50% of the transverse diameter of the chest (increased cardiothoracic ratio). At the time of entry into the study 110 subjects (23%) had cardiomegaly. After 10 years, 51% of the subjects with cardiomegaly at baseline died compared with 33% of the subjects without cardiomegaly (mortality rate = 9.1 vs 4.8/100 person-years respectively; p = 0.014). Cardiovascular disease incidence was also higher for those with preexisting cardiomegaly at baseline (rate 9.1 vs 6.1/100 person-years; p = 0.0001). According to the Cox proportional hazards regression analysis, age, cardiomegaly, diabetes, and prior evidence of myocardial infarction were independent predictors for death in this cohort. Similarly, the best predictive variables for cardiovascular disease were age, diabetes, prior evidence of myocardial infarction, and cigarette smoking. Of the 359 subjects without cardiomegaly at baseline, 108 (30%) showed evidence of new cardiomegaly, and their risk of cardiovascular disease was 1.8 times that of subjects whose test results were negative for cardiomegaly throughout the study (p = 0.003). Thus cardiomegaly, as defined by an increased cardiothoracic ratio on x-ray films, irrespective of cause, is associated with a poor prognosis in very elderly men and women.


Assuntos
Idoso de 80 Anos ou mais , Envelhecimento , Cardiomegalia/epidemiologia , Doenças Cardiovasculares/epidemiologia , Idoso , Cardiomegalia/diagnóstico por imagem , Estudos de Coortes , Feminino , Humanos , Incidência , Estudos Longitudinais , Masculino , Prevalência , Prognóstico , Modelos de Riscos Proporcionais , Estudos Prospectivos , Radiografia , Fatores de Risco
4.
J Bacteriol ; 137(2): 900-4, 1979 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-154510

RESUMO

A method is described which permits the selection of mutants of Neurospora crassa that are deficient in succinic dehydrogenase activity. The method relies on the observation that succinic dehydrogenase-deficient strains fail to reduce the dye nitrotetrazolium blue when overlaid with the dye in the presence of succinate and phenazine methosulfate. Wild-type colonies reduced the dye and turned blue, whereas mutant colonies remained colorless. In this communication we present studies of a mutant, SDH-1, isolated by this method. The mutant had 18% of the succinic dehydrogenase activity of the parent strain used in the mutation experiments as determined from the ratio of Vmax activities obtained from Lineweaver-Burk plots. The SDH-1 mutant segregated in a Mendelian manner when back-crossed to its parent strain. Succinate oxidase activity in SDH-1 was low and was markedly inhibited by adenosine 5'-diphosphate. The succinate oxidase activity of the parent strain was high and was not affected by the presence of adenosine 5'-diphosphate.


Assuntos
Mutação , Neurospora crassa/genética , Neurospora/genética , Succinato Desidrogenase/genética , Neurospora crassa/isolamento & purificação , Neurospora crassa/metabolismo , Nitroazul de Tetrazólio/metabolismo , Oxirredução , Succinatos/metabolismo
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