![]() | Carl GrunfeldMedical Service, San Francisco Veterans Affairs Health Care System, San Francisco, CA, USA | San Francisco Veterans Affairs Health Care System, Research Service and Division ... |
KOL Resume for Carl Grunfeld
Year | |
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2022 | Medical Service, San Francisco Veterans Affairs Health Care System, San Francisco, CA, USA |
2021 | Kidney Health Research Collaborative, Department of Medicine, San Francisco Veterans Affairs Health Care System and University of California, San Francisco, CA, USA |
2019 | Metabolism Section, Veterans Affairs Medical Center, San Francisco, California Kidney Health Research Collaborative, Department of Medicine, San Francisco Veterans Affairs Healthcare System. |
2018 | Department of Medicine, University of California-San Francisco, California. |
2017 | University of California, Veterans Affairs Medical Center, San Francisco, California |
2016 | Department of Medicine UCSF, San Francisco Veterans Affairs Medical Center, University of California, San Francisco, San Francisco, CA Veterans Affairs Medical Center, San Francisco, California, USA |
2015 | Medical Service, Department of Veteran Affairs Medical Center, San Francisco, California |
2014 | Department of Medicine, San Francisco Veterans Affairs Medical Center, San Francisco, CA |
2013 | Department of Medicine, San Francisco Veterans Affairs Medical Center, and University of California, San Francisco, San Francisco, California San Francisco VA Medical Center, 4150 Clement Street (116-P), San Francisco, CA 94121 USA |
2012 | Metabolism Section, Department of Veterans Affairs Medical Center, University of California, San Francisco, San Francisco, California, USA Department of Medicine, San Francisco Veterans Affairs Medical Center Editorial Board |
2011 | Division of Metabolism and Endocrine Sections, San Francisco VA Medical Center; San Francisco, CA, USA 2, Department of Medicine, University of California, San Francisco, California |
2010 | From the Department of Medicine, San Francisco Veterans Affairs Medical Center, and University of California, San Francisco (A.I.C., Y.L., C.G., P.A.V., M.G.S.); Department of Epidemiology and Biostatistics, University of California, San Francisco (A.I.C., M.G.S.); and Positive Health Program, San Francisco General Hospital, San Francisco, Calif (S.G.D.). San Francisco Veterans Affairs Medical Center, San Francisco, CA Department of Medicine, University of California, USA, Division of Endocrinology and Metabolism, Department of Veterans Affairs Medical Center, USA |
Carl Grunfeld: Influence Statistics
Concept | World rank |
---|---|
hepatic lipogenesis | #1 |
tnfα pepck | #1 |
anticandidal protein hdl | #1 |
content glccer | #1 |
mrna levels papss2 | #1 |
insulin receptor proteolysis | #1 |
lpdp ability | #1 |
oxidation sepsis | #1 |
monocytes hivinfected subjects | #1 |
tnf lps activation | #1 |
transport protein fatp | #1 |
ppargamma lxralpha | #1 |
lta lipoprotein lipase | #1 |
chow sesame oil | #1 |
caloric intake levels | #1 |
chylomicrons death | #1 |
125ilabeled betaglucan | #1 |
gpat1 pparγ | #1 |
pad leptin levels | #1 |
lpsinduced decrease pepck | #1 |
mrna levels fat | #1 |
fibrinogen clinical measures | #1 |
hepatic sphingolipid synthesis | #1 |
redistribution metabolic | #1 |
hepatic expression pcsk9 | #1 |
lps plscr1 mrna | #1 |
lps kidney | #1 |
lta macrophage production | #1 |
urea treatment dithiothreitol | #1 |
nefa levels subchronic | #1 |
insulinomimetic activity desensitization | #1 |
insulin kidney insulin | #1 |
height body women | #1 |
282 reports | #1 |
race groups latinos | #1 |
pad resistin | #1 |
il1 decrease | #1 |
cntf lipid metabolism | #1 |
impact lipohypertrophy | #1 |
tgs oxidation | #1 |
il1 mtp | #1 |
pis egp | #1 |
hyperlipidemia protease inhibitors | #1 |
vldl vldl production | #1 |
car apr | #1 |
hca2 pathways | #1 |
dermis tapestripping | #1 |
liver functional consequences | #1 |
ypr016c saccharomyces | #1 |
innate lipoproteins hdl | #1 |
Open the FULL List in Excel | |
Prominent publications by Carl Grunfeld
Endotoxin down-regulates ABCG5 and ABCG8 in mouse liver and ABCA1 and ABCG1 in J774 murine macrophages differential role of LXR
[ PUBLICATION ]
Several of the ATP binding cassette (ABC) transporters have recently been shown to play important roles in reverse cholesterol transport (RCT) and prevention of atherosclerosis. In the liver, ABCG5 and ABCG8 have been proposed to efflux sterols into the bile for excretion. ABCG5 and ABCG8 also limit absorption of dietary cholesterol and plant sterols in the intestine. In macrophages, ABCA1 and ABCG1 mediate cholesterol removal from these cells to HDL. Many of these ABC transporters are ...
Known for Messenger Receptors | Abca1 Abcg1 | Abcg5 Abcg8 | Binding Cassette | Murine Macrophages |
Peroxisome proliferator-activated receptors (PPARs) are transcription factors that play an important role in the regulation of genes involved in lipid utilization and storage, lipoprotein metabolism, adipocyte differentiation, and insulin action. The three isoforms of the PPAR family, i.e. alpha, delta, and gamma, have distinct tissue distribution patterns. PPAR-alpha is predominantly present in the liver, and PPAR-gamma in adipose tissue, whereas PPAR-delta is ubiquitously expressed. A ...
Known for Expression Liver | Adipose Tissue | Ppar Gamma | Fat Cd36 | Messenger Receptors |
During the acute phase response, cytokines induce marked alterations in lipid metabolism including an increase in serum triglyceride levels and a decrease in hepatic fatty acid oxidation, in bile acid synthesis, and in high-density lipoprotein levels. Here we demonstrate that tumor necrosis factor (TNF) and interleukin 1 (IL-1), but not IL-6, decrease the expression of retinoid X receptor alpha (RXRalpha), peroxisome proliferator-activated receptor alpha (PPARalpha), PPARgamma, liver X ...
Known for Tumor Necrosis | Messenger Receptors | Pparalpha Ppargamma | Nuclear Receptor | Mrna Levels |
Regulation of putative fatty acid transporters and Acyl-CoA synthetase in liver and adipose tissue in ob/ob mice.
[ PUBLICATION ]
The hyperlipidemia associated with obesity and type 2 diabetes is caused by an increase in hepatic triglyceride synthesis and secretion that is secondary to an increase in de novo lipogenesis, a decrease in fatty acid (FA) oxidation, and an increase in the flux of peripherally derived FA to the liver. The uptake of FA across the plasma membrane may be mediated by three distinct proteins--FA translocase (FAT), plasma membrane FA binding protein (FABP-pm), and FA transport protein ...
Known for Adipose Tissue | Liver Mice | Acid Transport | Proteins Fatty | Coa Synthetase |
Regulation of fatty acid transport protein and fatty acid translocase mRNA levels by endotoxin and cytokines
[ PUBLICATION ]
The cloning of two novel fatty acid (FA) transport proteins, FA transport protein (FATP) and FA translocase (FAT), has recently been reported; however, little is known about their in vivo regulation. Endotoxin [lipopolysaccharide (LPS)], tumor necrosis factor (TNF), and interleukin-1 (IL-1) stimulate adipose tissue lipolysis and enhance hepatic lipogenesis and reesterification while suppressing FA oxidation in multiple tissues. Hence, in this study we examined their effects on FATP and ...
Known for Fatty Acid | Transport Protein | Fatp Fat | Liver Oxidation | Reesterification Lps |
LPS and cytokines regulate extra hepatic mRNA levels of apolipoproteins during the acute phase response in Syrian hamsters
[ PUBLICATION ]
Altered hepatic expression of apolipoproteins occurs during the acute phase response. Here we examined whether the acute phase response alters extra hepatic expression of apolipoproteins. Syrian hamsters were injected with endotoxin (LPS), tumor necrosis factor (TNF), interleukin (IL)-1, or the combination of TNF + IL-1 and mRNAs for serum amyloid A (apoSAA), apolipoprotein (apo) J, apo E. apo A-I, and apo D, were analyzed. LPS increased mRNA levels for apoSAA in all tissues examined. ...
Known for Acute Phase Response | Mrna Levels | Lps Tnf | Syrian Hamsters | Tumor Necrosis |
Downregulation of liver X receptor-α in mouse kidney and HK-2 proximal tubular cells by LPS and cytokines
[ PUBLICATION ]
The acute-phase response (APR) suppresses type II nuclear hormone receptors and alters the expression of their target genes involved in lipid metabolism in the liver and heart. Therefore, we examined the expression of liver X receptor/retinoid X receptor (LXR/RXR) and their target genes in kidney from mice treated with lipopolysaccharide (LPS) and in human proximal tubular HK-2 cells treated with interleukin-1beta (IL-1beta) and tumor necrosis factor-alpha (TNF-alpha). We found that ...
Known for Messenger Receptors | Receptor Alpha | Lipid Metabolism | Target Genes | Expression Nuclear |
The extracellular lipids of the stratum corneum, which are comprised mainly of cholesterol, fatty acids, and ceramides, are essential for epidermal permeability barrier function. Moreover, disruption of the permeability barrier results in an increased cholesterol, fatty acid, and ceramide synthesis in the underlying epidermis. This increase in lipid synthesis has been shown previously to be due to increased activities of HMG-CoA reductase, acetyl-CoA carboxylase, fatty acid synthase and ...
Known for Fatty Acid | Permeability Barrier | Ceramide Synthesis | Mrna Levels | Enzymes Cholesterol |
Hyperlipidemia frequently accompanies infectious diseases and may be due to increases in lipoprotein production or decreases in lipoprotein clearance. The administration of endotoxin (LPS) has been used to mimic infection and prior studies demonstrate that LPS produces hypertriglyceridemia. In the present study in rodents, the dose of LPS necessary to induce hyperlipidemia was orders of magnitude less than that necessary to induce shock and death. As little as 10 ng/100 g body weight ...
Known for Hepatic Triglyceride | Low Dose | Lipid Metabolism | Endotoxin Lps | Lipoprotein Production |
The host response to infection is associated with several alterations in lipid metabolism that promote lipoprotein production. These changes can be reproduced by lipopolysaccharide (LPS) administration. LPS stimulates hepatic cholesterol synthesis and suppresses the conversion of cholesterol to bile acids. LPS down-regulates hepatic cholesterol 7alpha-hydroxylase, the rate-limiting enzyme in the classic pathway of bile acid synthesis. We now demonstrate that LPS markedly decreases the ...
Known for Hepatocyte Nuclear Factor | Sterol 27 | Acute Phase | Bile Acid Synthesis | Mrna Levels |
Risk Factors for ESRD in HIV-Infected Individuals: Traditional and HIV-Related Factors
[ PUBLICATION ]
BACKGROUND: Despite improvements in survival with human immunodeficiency virus (HIV) infection, kidney disease remains an important complication. Few studies have evaluated risk factors associated with the development of end-stage renal disease (ESRD) in HIV-infected individuals. We sought to identify traditional and HIV-related risk factors for ESRD in HIV-infected individuals and compare ESRD risk by estimated glomerular filtration rate (eGFR) and proteinuria levels.
STUDY DESIGN: ...
Known for Infected Individuals | Kidney Disease | Risk Factors Esrd | Hepatitis Virus Coinfection | Diabetes Complications |
Endotoxin and TNF lead to reduced plasma LCAT activity and decreased hepatic LCAT mRNA levels in Syrian hamsters.
[ PUBLICATION ]
Endotoxin (LPS) administration, which mimics infection, stimulates the production of many cytokines, including TNF, that are thought to mediate the alterations in lipid metabolism that occur during infection. The aims of this study were to determine the effect of LPS or TNF administration on plasma LCAT activity and hepatic LCAT mRNA levels in Syrian hamsters. Plasma LCAT activity was decreased 8 h after LPS administration, reached a maximum level of inhibition at 16 h which persisted ...
Known for Mrna Levels | Syrian Hamsters | Lcat Activity | Lps Administration | Lipid Metabolism |
Key People For Hiv Infection
Carl Grunfeld:Expert Impact
Concepts for whichCarl Grunfeldhas direct influence:Hiv infection, Tumor necrosis factor, Adipose tissue, Mrna levels, Lipid metabolism, Insulin receptor, Insulin resistance, Body composition.
Carl Grunfeld:KOL impact
Concepts related to the work of other authors for whichfor which Carl Grunfeld has influence:Insulin receptor, Hiv infection, Adipose tissue, Antiretroviral therapy, Metabolic syndrome, Cardiovascular disease, Lipid metabolism.
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