The Research Center for Clinical Pharmacology and Drug Toxicology consists of clinical pharmacologists working in association with a nucleus of investigators whose research in biochemical pharmacology includes the biotransformation of drugs, analytical pharmacology and pharmacokinetics. The specific resources in the Center enable application of the best available techniques and approaches to studies of drugs in man and provide an environment for training investigators in clinical pharmacology. The research program will focus on the metabolism, distribution and biochemical effects of drugs in man. Within this framework, attention will be given to the delineation of interactions between drugs in patients and to the development of knowledge that will enable prediction of drug toxicity. The relevance of the marked interindividual difference in the plasma levels of certain drugs to their efficacy and toxicity will be investigated as well as the influence of disease processes and age on patients' response to drugs. A further related aim will be the development of analytical techniques for accurately measuring nanogram amounts of drugs and metabolites in body fluids, including approaches such as selected-ion-monitoring with the mass spectrometer and improved application of high pressure liquid chromatography. The clinical pharamcology of drugs for the treatment of cardiac arrhythmias and hypertension will be studied. The pharmacology of the prostaglandins and thromboxanes and their relation to disease processes is under investigation with emphasis on the participation of arachidonic acid metabolites in the acute allergic response, the clinical pharamcology of anti-inflammatory drugs used in arthritis, the regulation of platelet aggregation and the development of quantitative methods for measuring thromboxane and prostacyclin production in man. The biotransformation of drugs to active and inactive metabolites as well as their distribution, transport, binding and biochemical effects in a variety of species will be investigated in an attempt to provide a rational basis for the prediction of their effects and toxicity in man.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Specialized Center (P50)
Project #
5P50GM015431-19
Application #
3105988
Study Section
Pharmacology-Toxicology Review Committee (PTR)
Project Start
1977-12-01
Project End
1987-11-30
Budget Start
1985-12-01
Budget End
1986-11-30
Support Year
19
Fiscal Year
1986
Total Cost
Indirect Cost
Name
Vanderbilt University Medical Center
Department
Type
Schools of Medicine
DUNS #
004413456
City
Nashville
State
TN
Country
United States
Zip Code
37203
Salisbury-Ruf, Christi T; Bertram, Clinton C; Vergeade, Aurelia et al. (2018) Bid maintains mitochondrial cristae structure and function and protects against cardiac disease in an integrative genomics study. Elife 7:
Kong, Deping; Li, Juanjuan; Shen, Yujun et al. (2017) Niacin Promotes Cardiac Healing after Myocardial Infarction through Activation of the Myeloid Prostaglandin D2 Receptor Subtype 1. J Pharmacol Exp Ther 360:435-444
Teder, Tarvi; Boeglin, William E; Brash, Alan R (2017) Oxidation of C18 Hydroxy-Polyunsaturated Fatty Acids to Epoxide or Ketone by Catalase-Related Hemoproteins Activated with Iodosylbenzene. Lipids 52:587-597
Plewes, Katherine; Kingston, Hugh W F; Ghose, Aniruddha et al. (2017) Cell-free hemoglobin mediated oxidative stress is associated with acute kidney injury and renal replacement therapy in severe falciparum malaria: an observational study. BMC Infect Dis 17:313
Kudalkar, Shalley N; Kingsley, Philip J; Marnett, Lawrence J (2016) Assay of Endocannabinoid Oxidation by Cyclooxygenase-2. Methods Mol Biol 1412:205-15
Wu, Jing; Montaniel, Kim Ramil C; Saleh, Mohamed A et al. (2016) Origin of Matrix-Producing Cells That Contribute to Aortic Fibrosis in Hypertension. Hypertension 67:461-8
Wu, Jing; Saleh, Mohamed A; Kirabo, Annet et al. (2016) Immune activation caused by vascular oxidation promotes fibrosis and hypertension. J Clin Invest 126:50-67
Mashhadi, Zahra; Newcomer, Marcia E; Brash, Alan R (2016) The Thr-His Connection on the Distal Heme of Catalase-Related Hemoproteins: A Hallmark of Reaction with Fatty Acid Hydroperoxides. Chembiochem 17:2000-2006
Kong, Deping; Shen, Yujun; Liu, Guizhu et al. (2016) PKA regulatory II? subunit is essential for PGD2-mediated resolution of inflammation. J Exp Med 213:2209-26
Boutaud, Olivier; Sosa, I Romina; Amin, Taneem et al. (2016) Inhibition of the Biosynthesis of Prostaglandin E2 By Low-Dose Aspirin: Implications for Adenocarcinoma Metastasis. Cancer Prev Res (Phila) 9:855-865

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