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T2 Electives - Department of Physiology

2008 - 2009 Academic Year

 
 


Experimental Physiology Course (Spring Semester)

Goals and Objectives:

The course will focus on the basic functions of cardiovascular, renal, gastrointestinal, reproductive, neuro-muscular and cellular transport systems using anesthetized animal models (dogs/pigs, rats, rabbits, frogs, etc.) as well as human volunteers.  The student will practice some basic simple surgical procedures in anesthetized animals and will formulate experimental design and research ideas aimed at strengthening the foundations of their medical, surgical and research training. 

Students in this course will: 

  1. learn fundamental regulatory mechanisms of some basic organs in a living system.
  2. practice simple surgical procedures on a living animal.
  3. acquire basic experience in conducting biological research in-vivo/in-vitro animal models.
  4. consider the ethics of using animals in research.

Methods of Instruction: The course will consist of laboratory exercises, research orientation and group discussions.  Students will work in a group under the guidance of the instructor.

Course Director: Dr. Dewan Majid, MD, PhD

Instructors: Dr. D. Majid, MD, PhD; Dr. K.D.Mitchell, PhD; Dr. Ming Li, PhD; Dr. Tino Unlap, PhD; Dr. Fady Botros, PhD; Dr. S. Abdournur, PhD.

Grading Policy: A grade of satisfactory or unsatisfactory will be determined on the basis of attendance and participation.  Letter grades will be given to the graduate students.  There will be no written exam.  Attendance is mandatory.  Excused absences may be granted only by the Dean, Department Chair or
Instructors.Enrollment: 4 to 16 students: T-1, T-2 and graduate students
Time of course: 16 weeks; Four hours per week (Friday, 1pm to 5pm) Sessions 3 & 4
Prerequisite: Medical/Graduate students who have taken/will take the medical physiology course.

Physiology Research

Students will participate in close association with their preceptor in ongoing research activities.

1. Renal and Vascular Physiology and Pathophysiology of Hypertension

Dr. L.G. Navar

office: room 4002, SOM

phone: 988-5252

e-mail: navar@tulane.edu

Dr. K. D. Mitchell

office: room 4055, SOM

phone: 988-2593

e-mail: kdmitch@tulane.edu

Dr. D. Majid

office: room 4020, SOM

phone: 988-2600

e-mail: majid@tulane.edu

Dr. H. Kobori

office: room M720B, SOM

phone: 988-2591

e-mail: hkobori@tulane.edu

Dr. M. Prieto-Carrasquero

office: room 4061, SOM

phone: 988-2445

e-mail: mprieto@tulane.edu

Dr. F. Botros

office: room 4059, SOM

phone: 988-8244

e-mail: fbotros@tulane.edu

 

 

 

 

Several faculty members, led by our Chairman, Dr. L.G. Navar, are investigating the role of the kidney and blood vessels in the pathophysiology of hypertension.  Students will be exposed to various experimental approaches used in the study of renal function, hemodynamics, tubular transport processes, and fluid and electrolyte regulation. Student can learn techniques for the evaluation of renal function, renal tubule reabsorption, and vascular responses to different antihypertensive drugs, as well as the expression and regulation of genes involved in hypertension.   Basic methodological approaches also will be covered in a systematic manner. The remainder of the student's time will be spent in one or more laboratories of participating faculty.

    2.  Molecular Physiology of Signal Transduction in Hypertension and           Cardiovascular Regulation

            Dr. K. Pandey     office: room 4022, SOM, phone: 988-1628; e-mail:           kpandey@tulane.edu

Dr. Pandey’s laboratory is studying the role of vasoactive natriuretic peptide hormones and their receptors in the pathophysiology of hypertension and cardiovascular regulation.  The ongoing studies include: molecular cloning and site-directed mutagenesis, gene transcription and expression, and cGMP-dependent transmembrane signaling mechanisms. The student will be exposed to a number of modern cellular and molecular approaches to delineate the genetic basis of hypertension and cardiovascular disorders both in vitro using cell culture systems and in vivo using gene-targeted mouse models 

      3.  Neurophysiology – Protection of Brain Cells from Ischemic Injury
           
Dr. N. Kreisman      office: room 4063, SOM, phone: 988-2590; e-mail:    nkreism@tulane.edu

Dr. Kreisman is investigating signaling mechanisms underlying selective vulnerability to anoxic/ischemic injury in the hippocampus and mechanisms of protection afforded by hypothermia and pre-ischemic conditioning.  Students will read background literature, learn electrophysiological and optical recording techniques, and perform experiments pertinent to their projects.

4.  Cellular Signaling Physiology

       Dr. M. Li                office: room 4724 SOM, phone: 988-8207;  e-mail:    mli@tulane.edu

Dr. Li’s research is focused on the cellular signaling mechanisms of insulin secretion and cancer cell proliferation.  In particular, Dr. Li is studying intracellular calcium signaling and the role of calcium ion channels in the progression of diabetes mellitus and breast and prostate cancer.  Students will employ fluorescence imaging and patch clamp techniques to investigate the role of calcium ion channels in hormone secretion and in cell proliferation.

  1. Molecular Physiology of Blood Vessels

      Dr. K. Matrougui   office: room 4008 SOM; phone 988-2588

      kmatroug@tulane.edu           

Dr. Matrougui’s lab is investigating signaling pathways that contribute to vascular dysfunction and structural wall remodeling of resistance arteries, particularly in diabetes and hypertension.  co-presentation of the two risk factors (hypertension and diabetes) exacerbates vascular disease but mechanisms are poorly understood.  Specifically they are studying the role of (1) advanced glycation end products, (2) epidermal growth factor receptor, (3) alphav-beta3-integrin, (4) transforming growth factor beta1 and (5) oxidative stress in coronary arterioles and mesenteric resistance arteries in animal models of these two diseases.   Experiments utilize integrative approaches including: pharmacology, molecular biology in vitro and in vivo adenovirus-siRNA mediated delivery, real time RT-PCR, western blot analysis, immunostaining, mitochondrial oxidative stress, primary cultures of vascular smooth muscle, and assessment of changes in morphology and stiffness of resistance arteries from hypertensive or diabetic mice.

Please see individual faculty members directly or contact Dr. Norman Kreisman, Overall Coordinator
Email: nkreism@tulane.edu     Phone: (504) 988-2590     Fax: (504) 988-2675
Mailing Address: 1430 Tulane Ave., SL-39, New Orleans, LA 70112
Enrollment: 1-8 students; T-1, T-2, T-4
Time of course: 4-8 hours per session for 2 sessions: Wednesday and/or Friday: 1:00-5:00 p.m.
Sessions 1 and 2, Sessions 3 and 4
Prerequisite: Instructor's approval and brief prospectus.


Other elective opportunities are described below and may include departmental research projects that are done under faculty supervision.

 
   
Last Updated May 5, 2008

 

 

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