Gene/Protein Disease Symptom Drug Enzyme Compound
Pivot Concepts:   Target Concepts:
Query: EC:1.3.5.1 (succinate dehydrogenase)
 8,177 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The mediated electro-enzymatic electrolysis systems based on the tricarboxylic acid (TCA) cycle reaction were examined on a micro-bulk electrolytic system. A series of the enzyme-catalyzed reactions in the TCA cycle was coupled with electrode reaction. Electrochemical oxidation of NADH was catalyzed by diaphorase with an aid of a redox mediator with a formal potential of -0.15 V vs. Ag|AgCl. The mediator was also able to shuttle electrons between succinate dehydrogenase and electrode. The charge during the electrolysis increased on each addition of dehydrogenase reaction in a cascade of the TCA cycle. However, the electrolysis efficiencies were close to or less than 90% because of the product inhibition. Lactate oxidation to acetyl-CoA catalyzed by two NAD-dependent dehydrogenases was coupled with the bioelectrochemical TCA cycle reaction to achieve the 12-electron oxidation of lactate to CO(2). The charge passed in the bioelectrocatalytic oxidation of 5 nmol of lactate was 4 mC, which corresponds to 70% of the electrolysis efficiency.
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PMID:Micro-coulometric study of bioelectrochemical reaction coupled with TCA cycle. 2239 82

The aim of the study was the estimation of structural and metabolic changes in the rat cerebellum Purkinje cells (PC) in the dynamics of subhepatic cholestasis. Histological, histochemical and electron microscopic methods were used. It was found that the cholestasis induced the progressive intensification of the structural and metabolic disturbances in the cerebellar PC reaching their maximum on days 10-20 and resulting in PC death and PC number reduction. In the cytoplasm of these cells the reduction of the activities of succinate dehydrogenase, NADH-diaphorase, glucose-6-dehydrogenase was recorded together with the decrease of RNA content and the activation of lactate dehydrogenase and acid phosphatase. The disturbances of PC at the ultrastructural level included the destruction of the nucleus and organelles (especially, of the mitochondria), associated with the increase of phagosome size and number, augmentation of relative free ribosome number, appearance of close contacts between mitichondria and cell nucleus and organelles. After 45-90 days in survived animals gradual normalization of PC structure and metabolism took place apparently as a result of spontaneous cholestasis elimination due to the development of new bile ducts.
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PMID:[Structural and histochemical changes in the rat cerebellum Purkinje cells after cholestasis]. 2389 17

Psychological stress is an important perpetuating, worsening and risk factor for temporomandibular disorders of muscular or articular origin. Occlusion instability, by the way, is considered a risk factor of this pathology and can be reproduced in some experimental animal models. The exact physiologic mechanism underlying these relations however, remains unclear. Our purpose was to test the hypothesis that chronic stress and unilateral exodontia induce metabolic and vascular changes in the medial pterygoid muscle of rats. Adult Wistar rats were submitted to chronic unpredictable stress and/or unilateral exodontia and their plasma and medial pterygoid muscle were removed for analysis. The parameters evaluated included plasma levels of corticosterone, metabolic activity by succinate dehydrogenase, oxidative capacity by nicotinamide adenine dinucleotide diaphorase, capillary density by laminin and alfa-CD staining and reactive oxidative species production. Chronic unpredictable stress as an isolated factor, increased oxidative metabolism, capillary density and reactive oxygen species production at medial pterygoid muscle. Conversely, exodontia has a main effect in metabolism, promoting glycolytic transformation of muscle fibers. Association of both factors induced a major glycolytic pattern in muscle and vascular changes. Our findings provide insights into the mechanisms, possibly inducing metabolic and vascular alterations on medial pterygoid muscle of rats, by which chronic stress and occlusal instabilities might be involved as risk factors in the pathophysiology of temporomandibular disorders with muscular components.
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PMID:Metabolic and vascular pattern in medial pterygoid muscle is altered by chronic stress in an animal model of hypodontia. 2927


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