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1.
Genome ; 64(4): 355-371, 2021 Apr.
Article in English | MEDLINE | ID: mdl-33031715

ABSTRACT

The gut-brain axis (GBA) is a biochemical link that connects the central nervous system (CNS) and enteric nervous system (ENS). Clinical and experimental evidence suggests gut microbiota as a key regulator of the GBA. Microbes living in the gut not only interact locally with intestinal cells and the ENS but have also been found to modulate the CNS through neuroendocrine and metabolic pathways. Studies have also explored the involvement of gut microbiota dysbiosis in depression, anxiety, autism, stroke, and pathophysiology of other neurodegenerative diseases. Recent reports suggest that microbe-derived metabolites can influence host metabolism by acting as epigenetic regulators. Butyrate, an intestinal bacterial metabolite, is a known histone deacetylase inhibitor that has shown to improve learning and memory in animal models. Due to high disease variability amongst the population, a multi-omics approach that utilizes artificial intelligence and machine learning to analyze and integrate omics data is necessary to better understand the role of the GBA in pathogenesis of neurological disorders, to generate predictive models, and to develop precise and personalized therapeutics. This review examines our current understanding of epigenetic regulation of the GBA and proposes a framework to integrate multi-omics data for prediction, prevention, and development of precision health approaches to treat brain disorders.


Subject(s)
Brain Diseases/genetics , Epigenesis, Genetic , Gastrointestinal Microbiome/physiology , Machine Learning , Animals , Artificial Intelligence , Bacteria/genetics , Brain , Data Analysis , Dysbiosis , Fatty Acids, Volatile , Humans
2.
Biochem Cell Biol ; 98(1): 12-22, 2020 02.
Article in English | MEDLINE | ID: mdl-31112654

ABSTRACT

Mortality and morbidity from cardiovascular diseases (CVDs) represents a huge burden to society. It is recognized that environmental factors and individual lifestyles play important roles in disease susceptibility, but the link between these external risk factors and our genetics has been unclear. However, the discovery of sequence-independent heritable DNA changes (epigenetics) have helped us to explain the link between genes and the environment. Multiple diverse epigenetic processes, including DNA methylation, histone modification, and the expression of non-coding RNA molecules affect the expression of genes that produce important changes in cellular differentiation and function, influencing the health and adaptability of the organism. CVDs such as congenital heart disease, cardiomyopathy, heart failure, cardiac fibrosis, hypertension, and atherosclerosis are now being viewed as much more complex and dynamic disorders. The role of epigenetics in these and other CVDs is currently under intense scrutiny, and we can expect important insights to emerge, including novel biomarkers and new approaches to enable precision medicine. This review summarizes the recent advances in our understanding of the role of epigenetics in CVD.


Subject(s)
Cardiovascular Diseases/genetics , Epigenesis, Genetic/genetics , Epigenomics , Humans
3.
Can J Physiol Pharmacol ; 90(2): 249-60, 2012 Feb.
Article in English | MEDLINE | ID: mdl-22316244

ABSTRACT

We tested whether the activation of proteolytic enzymes, calpain, and matrix metalloproteinases (MMPs) during ischemia-reperfusion (I/R) is mediated through oxidative stress. For this purpose, isolated rat hearts were subjected to a 30 min global ischemia followed by a 30 min reperfusion. Cardiac function was monitored and the activities of Na(+)/K(+)-ATPase, Mg(2+)-ATPase, calpain, and MMP were measured. Depression of cardiac function and Na(+)/K(+)-ATPase activity in I/R hearts was associated with increased calpain and MMP activities. These alterations owing to I/R were similar to those observed in hearts perfused with hypoxic medium, H(2)O(2) and xanthine plus xanthine oxidase. The I/R-induced changes were attenuated by ischemic preconditioning as well as by perfusing the hearts with N-acetylcysteine or mercaptopropionylglycine. Inhibition of MMP activity in hearts treated with doxycycline depressed the I/R-induced changes in cardiac function and Na(+)/K(+)-ATPase activity without affecting the calpain activation. On the other hand, inhibition of calpain activity upon treatment with leupeptin or MDL 28170 significantly reduced the MMP activity in addition to attenuating the I/R-induced alterations in cardiac function and Na(+)/K(+)-ATPase activity. These results suggest that the I/R-induced depression in Na(+)/K(+)-ATPase and cardiac function may be a consequence of the increased activities of both calpain and MMP because of oxidative stress in the heart.


Subject(s)
Calpain/metabolism , Matrix Metalloproteinases/metabolism , Myocardial Reperfusion Injury/enzymology , Myocardium/enzymology , Oxidative Stress , Sarcolemma/enzymology , Sodium-Potassium-Exchanging ATPase/metabolism , Animals , Antioxidants/pharmacology , Calpain/antagonists & inhibitors , Down-Regulation , Enzyme Activation , Hypoxia/enzymology , In Vitro Techniques , Ischemic Preconditioning, Myocardial , Male , Matrix Metalloproteinase Inhibitors , Myocardial Reperfusion Injury/physiopathology , Myocardial Reperfusion Injury/prevention & control , Oxidants/pharmacology , Oxidative Stress/drug effects , Perfusion , Protease Inhibitors/pharmacology , Rats , Rats, Sprague-Dawley , Sarcolemma/drug effects , Time Factors , Ventricular Function, Left , Ventricular Pressure
4.
Can J Physiol Pharmacol ; 88(3): 388-97, 2010 Mar.
Article in English | MEDLINE | ID: mdl-20393603

ABSTRACT

Depression in cardiac performance due to ischemia-reperfusion (I/R) injury is associated with the development of oxidative stress and decreased sarcolemmal (SL) Na+/K+-ATPase activity. Since both I/R and oxidative stress have been reported to promote the occurrence of intracellular Ca2+ overload and activate proteases such as calpain, this study was undertaken to investigate whether the activation of calpain in I/R hearts is associated with alterations in the SL Na+/K+-ATPase activity and its isoform content. For this purpose, isolated rat hearts treated with and without 2 different calpain inhibitors (leupeptin and MDL28170) were subjected to 30 min ischemia followed by 60 min of reperfusion, and the cardiac function, SL Na+/K+-ATPase activity, Na+/K+-ATPase isoform protein content, and calpain activity were measured. The I/R-induced depressions in cardiac function, Na+/K+-ATPase activity, and protein content of Na+/K+-ATPase isoforms were associated with an increase in calpain activity , but were prevented by treatment of hearts with leupeptin. Incubation of SL membranes with calpain decreased the Na+/K+-ATPase activity and protein content of its isoforms; these changes were also attenuated by leupeptin. The I/R-induced alterations in cardiac function and the activity of SL Na+/K+-ATPase and calpain were Ca2+-dependent and were prevented by MDL28170, a specific inhibitor of calpain. The I/R-induced translocation of calpain isoforms (I and II) from the cytosol to SL and the changes in distribution of calpastatin were also attenuated by treatment with calpain inhibitors. These results suggest that the depression in cardiac function and SL Na+/K+-ATPase activity in I/R hearts may be due to changes in the activity and translocation of calpain.


Subject(s)
Calpain/metabolism , Myocardial Reperfusion Injury/enzymology , Myocytes, Cardiac/enzymology , Sarcolemma/enzymology , Sodium-Potassium-Exchanging ATPase/metabolism , Animals , Calpain/antagonists & inhibitors , Dipeptides/pharmacology , Enzyme Activation/drug effects , Enzyme Activation/physiology , Male , Myocytes, Cardiac/drug effects , Protein Transport/drug effects , Protein Transport/physiology , Rats , Rats, Sprague-Dawley
5.
J Appl Physiol (1985) ; 105(6): 1779-87, 2008 Dec.
Article in English | MEDLINE | ID: mdl-18832762

ABSTRACT

Isolated hearts subjected to ischemia-reperfusion (I/R) exhibit depressed cardiac performance and alterations in subcellular function. Since hearts perfused at constant flow (CF) and constant pressure (CP) show differences in their contractile response to I/R, this study was undertaken to examine mechanisms responsible for these I/R-induced alterations in CF-perfused and CP-perfused hearts. Rat hearts, perfused at CF (10 ml/min) or CP (80 mmHg), were subjected to I/R (30 min global ischemia followed by 60 min reperfusion), and changes in cardiac function as well as sarcolemmal (SL) Na(+)-K(+)-ATPase activity, sarcoplasmic reticulum (SR) Ca(2+) uptake, and endothelial function were monitored. The I/R-induced depressions in cardiac function, SL Na(+)-K(+)-ATPase, and SR Ca(2+)-uptake activities were greater in hearts perfused at CF than in hearts perfused at CP. In hearts perfused at CF, I/R-induced increase in calpain activity and decrease in nitric oxide (NO) synthase (endothelial NO synthase) protein content in the heart as well as decrease in NO concentration of the perfusate were greater than in hearts perfused at CP. These changes in contractile activity and biochemical parameters due to I/R in hearts perfused at CF were attenuated by treatment with l-arginine, a substrate for NO synthase, while those in hearts perfused at CP were augmented by treatment with N(G)-nitro-l-arginine methyl ester, an inhibitor of NO synthase. The results indicate that the I/R-induced differences in contractile responses and alterations in subcellular organelles between hearts perfused at CF and CP may partly be attributed to greater endothelial dysfunction in CF-perfused hearts than that in CP-perfused hearts.


Subject(s)
Blood Pressure/physiology , Endothelium, Vascular/pathology , Reperfusion Injury/pathology , Acetylcholine/pharmacology , Animals , Calcium/metabolism , Calpain/metabolism , Coronary Vessels/enzymology , Coronary Vessels/metabolism , Cytosol/enzymology , Cytosol/metabolism , Endothelium, Vascular/enzymology , Male , Myocardial Contraction/physiology , Myocardium/enzymology , Nitric Oxide/biosynthesis , Nitric Oxide Synthase Type III/biosynthesis , Nitric Oxide Synthase Type III/metabolism , Perfusion , Rats , Rats, Sprague-Dawley , Reperfusion Injury/enzymology , Sarcolemma/enzymology , Sarcolemma/metabolism , Sarcoplasmic Reticulum/enzymology , Sarcoplasmic Reticulum/metabolism , Sodium-Potassium-Exchanging ATPase/metabolism
6.
Cardiovasc Res ; 69(1): 152-63, 2006 Jan.
Article in English | MEDLINE | ID: mdl-16125156

ABSTRACT

OBJECTIVE: Earlier studies have shown that impaired cardiac contractility in ischemia reperfusion (IR) is associated with alterations in sarcoplasmic reticulum (SR) function. Impaired release of nitric oxide (NO) has been reported during IR, while administration of NO donors, such as L-arginine (LA), has been shown to improve cardiac performance in IR hearts. We therefore investigated the mechanisms underlying the recovery of contractile function in IR hearts treated with LA. METHODS: Isolated rat hearts subjected to 30 min of global ischemia were reperfused for 60 min. The effects of LA on cardiac performance, SR function and its regulation were examined. RESULTS: IR-induced impairment in cardiac performance was associated with a reduction in SR function and its regulation. IR caused an increase in calpain activity and a decrease in the sarcolemmal and SR nitric oxide synthase (NOS) isoform protein content as well as cytosolic NO levels. Administration of LA prevented contractile dysfunction in IR hearts, which was associated with a recovery of SR function and SR regulation by protein phosphorylation. This was consistent with a recovery in protein levels of major SR Ca2+-cycling and Ca2+-regulatory proteins. LA treatment attenuated an increase in calpain activity, possibly by nitrosylation of calpain, and increased cytosolic NO levels and SR NOS protein content in IR hearts. DISCUSSION: These results suggest that LA administration improved cardiac contractility by preventing alterations in SR Ca2+ handling and calpain activation in IR hearts.


Subject(s)
Arginine/therapeutic use , Calpain/antagonists & inhibitors , Myocardial Reperfusion Injury/metabolism , Sarcoplasmic Reticulum/metabolism , Animals , Blotting, Western/methods , Calcium/metabolism , Calcium-Calmodulin-Dependent Protein Kinases/analysis , Calcium-Calmodulin-Dependent Protein Kinases/metabolism , Calpain/metabolism , Cyclic AMP-Dependent Protein Kinases/analysis , Cyclic AMP-Dependent Protein Kinases/metabolism , Enzyme Activation/drug effects , Male , NG-Nitroarginine Methyl Ester/pharmacology , Nitric Oxide Synthase/antagonists & inhibitors , Nitric Oxide Synthase/metabolism , Perfusion , Rats , Rats, Sprague-Dawley , Sarcoplasmic Reticulum/drug effects
7.
Mol Cell Biochem ; 263(1-2): 241-56, 2004 Aug.
Article in English | MEDLINE | ID: mdl-15524184

ABSTRACT

Cardiovascular disease is a major cause of death and thus a great deal of effort has been made in salvaging the diseased myocardium. Although various factors have been identified as possible causes of different cardiac diseases such as heart failure and ischemic heart disease, there is a real need to elucidate their role for the better understanding of the cardiac disease pathology and formulation of strategies for developing newer therapeutic interventions. In view of the intimate involvement of different types of proteases in maintaining cellular structure, the role of proteases in various cardiac diseases has become the focus of recent research. Proteases are present in the cytosol as well as are localized in a number of subcellular organelles in the cell. These are known to use extracellular matrix, cytoskeletal, sarcolemmal, sarcoplasmic reticular, mitochondrial and myofibrillar proteins as substrates. Work from different laboratories using a wide variety of techniques has shown that the activation of proteases causes alterations of a number of specific proteins leading to subcellular remodeling and cardiac dysfunction. Inhibition of protease action by different drugs and agents, therefore, has a clinical relevance and is expected to form a part of new treatment paradigm for improving heart function. This review examines the biochemistry and localization of some of the proteases in the cardiac tissue in addition to identification of the sites of action of some protease inhibitors.


Subject(s)
Heart Diseases/enzymology , Heart Diseases/physiopathology , Peptide Hydrolases/physiology , Animals , Calpain/metabolism , Heart Diseases/drug therapy , Humans , Lysosomes/enzymology , Matrix Metalloproteinases/metabolism , Mitochondria, Heart/enzymology , Muscle Proteins/metabolism , Myocardium/metabolism , Peptide Hydrolases/classification , Protease Inhibitors/pharmacology , Proteasome Endopeptidase Complex/metabolism , Substrate Specificity
8.
J Mol Cell Cardiol ; 37(1): 101-10, 2004 Jul.
Article in English | MEDLINE | ID: mdl-15242740

ABSTRACT

Ca(2+) overload and free-radical injury are two mutually non-exclusive phenomena suggested to cause myocardial ischemia-reperfusion (IR)-induced contractile dysfunction; however, the mechanisms underlying their effects are not clear. One possible mechanism is the proteolytic modification of proteins by Ca(2+)-dependent proteases, such as calpains, which are activated during Ca(2+) overload that occurs in IR. The sarcoplasmic reticulum (SR) plays a central role in mediating cardiac contractility and therefore any impairment in SR function will induce cardiac contractile dysfunction. We therefore investigated the possibility whether SR proteins were the target for calpain action in IR. Langendorff-perfused rat hearts were subjected to IR in the presence and absence of leupeptin, a calpain inhibitor and the effects of calpain inhibition was examined on cardiac performance, SR function, and its regulation by protein phosphorylation as well as expression of SR Ca(2+)-cycling and -regulatory proteins. Our results show a depression in cardiac contractile function and activation of calpain during IR. Treatment with leupeptin recovered cardiac contractile function and attenuated calpain activity in IR hearts. The cardioprotection observed upon leupeptin treatment was associated with improved SR function and regulation. The recovery in SR function and regulation was consistent with prevention of IR-induced decrease in the expression of key SR Ca(2+)-handling and -regulatory proteins. Our results suggest that a downregulation of SR proteins by calpain may be a mechanism by which Ca(2+) overload causes cardiac contractile dysfunction during IR.


Subject(s)
Calpain/metabolism , Reperfusion Injury , Sarcoplasmic Reticulum/metabolism , Animals , Blotting, Western , Calcium/metabolism , Calcium-Binding Proteins/metabolism , Calcium-Transporting ATPases/metabolism , Calsequestrin/metabolism , Cyclic AMP-Dependent Protein Kinases/metabolism , Cytosol/metabolism , Down-Regulation , Leupeptins/chemistry , Leupeptins/metabolism , Male , Myocardial Contraction , Myocardium/pathology , Perfusion , Phosphorylation , Protease Inhibitors/pharmacology , Rats , Rats, Sprague-Dawley , Ryanodine Receptor Calcium Release Channel/metabolism , Sarcoplasmic Reticulum Calcium-Transporting ATPases , Time Factors
9.
Mol Cell Biochem ; 263(1): 241-56, 2004 Aug.
Article in English | MEDLINE | ID: mdl-27520682

ABSTRACT

Cardiovascular disease is a major cause of death and thus a great deal of effort has been made in salvaging the diseased myocardium. Although various factors have been identified as possible causes of different cardiac diseases such as heart failure and ischemic heart disease, there is a real need to elucidate their role for the better understanding of the cardiac disease pathology and formulation of strategies for developing newer therapeutic interventions. In view of the intimate involvement of different types of proteases in maintaining cellular structure, the role of proteases in various cardiac diseases has become the focus of recent research. Proteases are present in the cytosol as well as are localized in a number of subcellular organelles in the cell. These are known to use extracellular matrix, cytoskeletal, sarcolemmal, sarcoplasmic reticular, mitochondrial and myofibrillar proteins as substrates. Work from different laboratories using a wide variety of techniques has shown that the activation of proteases causes alterations of a number of specific proteins leading to subcellular remodeling and cardiac dysfunction. Inhibition of protease action by different drugs and agents, therefore, has a clinical relevance and is expected to form a part of new treatment paradigm for improving heart function. This review examines the biochemistry and localization of some of the proteases in the cardiac tissue in addition to identification of the sites of action of some protease inhibitors. (Mol Cell Biochem 263: 241-256, 2004).

10.
Exp Clin Cardiol ; 7(1): 40-53, 2002.
Article in English | MEDLINE | ID: mdl-19644578

ABSTRACT

Atherosclerosis is a leading cause of mortality and morbidity in the western world. It has been recognized for over a century, and the understanding of its pathogenesis has undergone many changes. Pathophysiological studies have unravelled the interactions of molecular and cellular elements involved in atherogenesis. The focus has shifted to the novel risk factors as well as characteristics and stability of atherosclerotic plaque; the genetic predisposition has further broadened the pathogenetic mechanisms. This review focuses on the molecular mechanisms involved in the evolution of the atherosclerotic plaque that may pave the way for selecting optimal therapies and preventing plaque complications. Atherosclerosis is no longer a disease attributed mainly to the high lipid content of the body. New insight into the disease pathology has shown it to be a disease of much greater ramifications. Endothelial damage and reactive oxygen species (and other free radicals) have predominantly emerged as factors in virtually all pathways leading to the development of atherosclerosis due to hyperlipidemia, diabetes, hypertension or smoking. Novel risk factors such as hyperhomocysteinemia, infections and systemic lupus erythematosus have emerged. Atherosclerosis has come to be regarded as a chronic inflammatory disease with an autoimmune component. The genetic basis of the disease assumes significance as candidate genes are identified and gene therapy becomes a promising new addition to the existing, less substantial conventional therapies.

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