The University of Michigan, Pharmacological Sciences and Bio-related Chemistry Training Program (PSTP) provides pre-doctoral students with a strong foundation in basic pharmacological principles and a broad knowledge of other bio-related basic science disciplines (e.g., medicinal chemistry). All students will complete a core curriculum consisting of courses in pharmacology, medicinal chemistry, physiology, and biostatistics, with other elective courses designed to fit the programmatic needs of individual students. Students may follow one of two general tracks with emphasis on biological or chemical research. Areas of research concentration within the program include cardiovascular/renal pharmacology, neuropharmacology, xenobiotic metabolism, growth and metabolic regulation, receptor structure and function, synthesis and pharmacology of therapeutic and diagnostic agents, antibiotic discovery, enzymology, transport mechanisms, drug absorption, drug delivery, and pharmacokinetics. Students obtain laboratory experience in several types of pharmacological research and learn how to design experiments, evaluate experimental data, and use appropriate statistical methods. The training program consists of two Phases. In Phase I, trainees engage in: graduate-level coursework, a qualifying examination for candidacy (halfway through Phase I), training in the responsible conduct of research, seminar programs, required research presentations at an Annual Symposium, and supervised laboratory investigation leading to the student's doctoral dissertation. In Phase II, th trainees participate in advanced training activities that address: career development (Career Night with PSTP alumni, Yellow School Bus trip to Pharma, Individual Career Development Plans), refresher RCR training, and professional development (Grant Writing Workshop, Peer Mentoring, Pedagogical Training). The training program culminates with a final oral examination during which the trainee defends his/her dissertation before their dissertation committee. Highly-qualified students, with an interest in obtaining advanced training in the pharmacological sciences that would not normally be available to them in their Ph.D. programs, are nominated by their Ph.D. program and mentor (PSTP faculty member) to the PSTP. Nominations are screened and nominees are assigned to either the Biological or Chemical Track based on their research and specific training interests. Nominees are evaluated (including interviews) by the PSTP Executive Committee, which makes the final appointment decisions. Students enter the PSTP at the beginning of their second year of graduate school and generally are financially supported by the training grant for two years during Phase I of the program. Trainees' progress is monitored by review of course grades, qualifying exams, laboratory experiences, and thesis work by both the trainees' Ph.D. programs and the PSTP to maintain a high level of quality. In Phase II, the trainee's progress is monitored by their mentor and by an additional PSTP faculty member via an annual dissertation committee meeting, with requisite written reports to the PSTP Directors. Support is requested for 14 trainees per year.

Public Health Relevance

The Pharmacological Sciences Training Program is designed to provide advanced training to students interested in pursuing research careers in the life sciences related to pharmacological research. An emphasis is placed on basic pharmacological principles and acquiring broad knowledge of related basic sciences like medicinal chemistry. The training provided to these future researchers will enable them to work on advances in medicine and human health related to drug therapy.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Institutional National Research Service Award (T32)
Project #
3T32GM007767-38S1
Application #
9275777
Study Section
Training and Workforce Development Subcommittee - B (TWD-B)
Program Officer
Okita, Richard T
Project Start
1978-07-01
Project End
2020-06-30
Budget Start
2016-07-01
Budget End
2017-06-30
Support Year
38
Fiscal Year
2016
Total Cost
$27,284
Indirect Cost
$2,021
Name
University of Michigan Ann Arbor
Department
Pharmacology
Type
Schools of Pharmacy
DUNS #
073133571
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Livingston, Kathryn E; Mahoney, Jacob P; Manglik, Aashish et al. (2018) Measuring ligand efficacy at the mu-opioid receptor using a conformational biosensor. Elife 7:
Masureel, Matthieu; Zou, Yaozhong; Picard, Louis-Philippe et al. (2018) Structural insights into binding specificity, efficacy and bias of a ?2AR partial agonist. Nat Chem Biol 14:1059-1066
Sanchez, Jaquelyn N; Wang, Ton; Cohen, Mark S (2018) BRAF and MEK Inhibitors: Use and Resistance in BRAF-Mutated Cancers. Drugs 78:549-566
Epling, Daniel; Hu, Yongjun; Smith, David E (2018) Evaluating the intestinal and oral absorption of the prodrug valacyclovir in wildtype and huPepT1 transgenic mice. Biochem Pharmacol 155:1-7
Drake, Lindsey R; Scott, Peter J H (2018) DARK Classics in Chemical Neuroscience: Cocaine. ACS Chem Neurosci 9:2358-2372
Lamberts, Jennifer T; Rosenthal, Lisa D; Jutkiewicz, Emily M et al. (2018) Role of the guanine nucleotide binding protein, G?o, in the development of morphine tolerance and dependence. Psychopharmacology (Berl) 235:71-82
Beyett, Tyler S; Gan, Xinmin; Reilly, Shannon M et al. (2018) Design, synthesis, and biological activity of substituted 2-amino-5-oxo-5H-chromeno[2,3-b]pyridine-3-carboxylic acid derivatives as inhibitors of the inflammatory kinases TBK1 and IKK? for the treatment of obesity. Bioorg Med Chem 26:5443-5461
Senese, Nicolas B; Oginsky, Max; Neubig, Richard R et al. (2018) Role of hippocampal 5-HT1A receptors in the antidepressant-like phenotype of mice expressing RGS-insensitive G?i2 protein. Neuropharmacology 141:296-304
Zwicker, Jeffery D; Diaz, Nicolas A; Guerra, Alfredo J et al. (2018) Optimization of dipeptidic inhibitors of cathepsin L for improved Toxoplasma gondii selectivity and CNS permeability. Bioorg Med Chem Lett 28:1972-1980
Stanczyk, M Alexander; Kandasamy, Ram (2018) Biased agonism: the quest for the analgesic holy grail. Pain Rep 3:e650

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