2009年3月30日 星期一

累積人生的智慧 [2009-03-31]

2009-03-30

 

「肯承認錯誤並虛心改進的人才能增長智慧。」

 

恭錄自 證嚴法師 所述的 [靜思語] 一書

 

 

2009-03-30

 
累積人生的智慧

 

「能夠不恥下問,可以虛心接受別人的批評,又能勇於承認自身的錯誤,並且願意針對問題之所在,主動進取地採取實際的行動,確確實實地著手去進行自我改革的人,自然就能夠與時俱進,不斷地累積出真正屬於自己的智慧。」

 

湯偉晉 WeiJin Tang 親手逐字地寫於 西元 2009-03-30

 

2009-03-31
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Keywords:
累積人生的智慧_[2009-03-31]
Number of attached files: 
1
 

2009年3月26日 星期四

2009年3月16日 星期一

Atherosclerosis is the principal cause of heart disease and a leading cause of stroke, making it the most common cause of death in the U.S. [2008](IR92)_FNKWs_{hydrogen peroxide, H2O2}





Atherosclerosis is the principal cause of heart disease and a leading cause of stroke, making it the most common cause of death in the U.S. [2008](IR92)


Atherosclerosis is the principal cause of heart disease and a leading cause of stroke, making it the most common cause of death in the U.S. [2008](IR92)_FNKWs_{hydrogen peroxide, H2O2}
http://www.vascularpath.org/projects.htm

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Essentially all risk factors for atherosclerosis result in the enhanced generation of hydrogen peroxide in the vessel wall by the activation of membrane bound NADPH oxidases (NOX). The NADPH oxidases generate superoxide in the extracellular space that both inactivates nitric oxide and is dismutated into hydrogen peroxide by extracellular superoxide dismutase (ECSOD).

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Atherosclerosis is the principal cause of heart disease and a leading cause of stroke, making it the most common cause of death in the U.S.

http://www.vascularpath.org/projects.htm
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Home | Projects | Lab Members | Publications | Links | Biographical Sketch | Contact

Projects

Atherosclerosis is the principal cause of heart disease and a leading cause of stroke, making it the most common cause of death in the U.S. The laboratory is seeking to understand the biochemical processes resulting in atherosclerosis in order to combat this pervasive disease.
Atherosclerosis is characterized by the development of necrotic/lipid cores within the intima of arteries at particular sites in the circulation. These necrotic/lipid cores form in the setting of a pre-existing intimal hyperplasia, characterized by the proliferation of smooth muscle-like cells within the intima. The laboratory is investigating both the mechanisms of signal transduction responsible for the formation of the pre-atherosclerotic intimal hyperplasia, as well as the factors stimulating the formation of intimal necrotic/lipid cores. Signal Transduction with Hydrogen Peroxide in Vascular Cells

Essentially all risk factors for atherosclerosis result in the enhanced generation of hydrogen peroxide in the vessel wall by the activation of membrane bound NADPH oxidases (NOX). The NADPH oxidases generate superoxide in the extracellular space that both inactivates nitric oxide and is dismutated into hydrogen peroxide by extracellular superoxide dismutase (ECSOD). These low physiologic levels of hydrogen peroxide are mitogenic, stimulating vascular cell growth and proliferation.

The mechanisms by which low endogenous levels of hydrogen peroxide stimulate cellular proliferation are currently poorly understood. The laboratory is using proteomic approaches with cultured vascular cells to identify signal transduction pathways activated by low physiologic levels of hydrogen peroxide. One target protein identified is the nuclear pre-mRNA binding protein hnRNP-C. Low physiologic levels of hydrogen peroxide stimulate the hyperphosphorylation of the acidic C-terminal domain of hnRNP-C, resulting in diminished ability of the protein to bind mRNA. The effect is mediate by protein kinase CK1 Other groups have previously shown that hnRNP-C is hyperphosphorylated during mitosis, and that CK1 entry into the nucleus is required for cell cycle progression. Proteomic Analyses of Intimal Hyperplasia from Atherosclerosis-Prone and Atherosclerosis-Resistant Human Arteries

Pre-atherosclerotic intimal hyperplasia forms at branch sites both in arteries prone to develop atherosclerosis, such as the internal carotid and coronary arteries and also in vessels remarkably resistant to the formation of atherosclerosis, such as the internal thoracic artery and the distal ulnar artery. The structural variations in intimal hyperplasia that may facilitate the development of atherosclerosis have been unclear. Proteoglycans have been implicated as playing a direct role in atherosclerosis, both by binding and retaining lipoproteins in the vessel wall and by regulating cell growth. One project in the laboratory has been to analyze by mass spectrometry the extracellular proteoglycans present in pre-atherosclerotic intimal hyperplasia from atherosclerosis-prone arteries as well as atherosclerosis-resistant arteries. This project has revealed the proteoglycan composition of human intimal hyperplasia to be more complex than previously realized with eight distinct proteoglycans present: perlecan, versican, aggrecan, biglycan, decorin, fibromodulin, lumican, and prolargin. Importantly, while most of the proteoglycans are present at similar levels in the two arterial types, there is a selective enhanced deposition of lumican proteoglycan in the pre-atherosclerotic intimal hyperplasia from the atherosclerosis-prone artery compared with the intimal hyperplasia from the atherosclerosis-resistant artery. This data
suggests that lumican may play a central role in the development of atherosclerotic lesions in humans, and may partly account for site-specific susceptibility to atherosclerosis. Home | Projects | Lab Members | Publications | Links | Biographical Sketch | Contact

Massachusetts General Hospital | Simches Building, Rm 8236
185 Cambridge Street, CPZN | Boston, MA 02114
Phone: 617-726-8303 | Fax: 617-726-2365

©2007 James R. Stone Lab - Department of Pathology - Massachusetts General Hospital

Site by: AlternaSite

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2009-03-17
File Index: 0001
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Keywords:
Hydrogen peroxide, increased, glutathione (GSH), L-Cysteine, Atherosclerosis (【醫學】動脈粥狀硬化), cardiovascular (【醫學】心血管性的), stroke (中風)

Number of attached files: 
3

2009年3月12日 星期四

穀胱甘肽(Glutathione)相關的研究報告 - 生老病死的秘密 at http://glutathione-research.blogspot.com and http://L-Cysteine.blogspot.com


2009-03-13
穀胱甘肽(Glutathione)相關的研究報告 - 生老病死的秘密 at http://glutathione-research.blogspot.com and http://L-Cysteine.blogspot.com

http://glutathione-research.blogspot.com

穀胱甘肽(Glutathione)相關的研究報告 - 生老病死的秘密
生老病死的秘密 - Glutathione (�胱甘肽), L-Cysteine (L-半胱氨酸), Hythiol-C (沛�旺-C); Glutathione (GSH) related research reports

http://L-Cysteine.blogspot.com

Keywords:
The Secret of Life and Death


2009年3月9日 星期一

The major determinants (決定因素) of GSH synthesis are the availability of cysteine, and the activity of the rate-limiting enzyme, g-glutamylcysteine synthetase (GCS)[1999](IR90)


The major determinants (決定因素) of GSH synthesis are the availability of cysteine, and the activity of the rate-limiting enzyme, g-glutamylcysteine synthetase (GCS)[1999](IR90)

Regulation of hepatic glutathione synthesis: current concepts and controversies SHELLY C. LU

USC Liver Disease Research Center, the Division of Gastrointestinal (胃腸的) and Liver Diseases, Department of Medicine, University of Southern California School of Medicine, Los Angeles, California 90033, USA

ABSTRACT

Glutathione (GSH) is an important intracellular peptide with multiple functions ranging from antioxidant defense to modulation of cell proliferation. GSH is synthesized in the cytosol (【生物學】細胞溶質) of all mammalian (哺乳動物()) cells in a tightly regulated manner. The major determinants (決定因素) of GSH synthesis are the availability of cysteine, the sulfur amino acid precursor, and the activity of the rate-limiting enzyme, g-glutamylcysteine synthetase (GCS). In the liver, major factors that determine the availability of cysteine are diet, membrane transport activities of the three sulfur amino acids cysteine, cystine and methionine, and the conversion of methionine to cysteine via the trans-sulfuration pathway. Many conditions alter GSH level via changes in GCS activity and GCS gene expression. These include oxidative stress, activators of Phase II detoxifying enzymes, antioxidants, drug-resistant tumor cell lines, hormones, cell proliferation, and diabetes mellitus (糖尿病). Since the molecular cloning (複製) of GCS, much has been learned about the regulation of this enzyme. Both transcriptional and post-transcriptional mechanisms modulate the activity of this critical cellular enzyme.

Lu, S. C. Regulation of hepatic glutathione synthesis: current concepts and controversies. FASEB J. 13, 1169-1183 (1999)

Key Words:
g-glutamylcysteine synthetase , cysteine availability , detoxification , antioxidant, rate-limiting substrate