Bibliography: leaves 180-199. / xvii, 199, [68] leaves, [1] leaf of plates : ill. ; 30 cm. / Title page, contents and abstract only. The complete thesis in print form is available from the University Library. / Primary aim was to determine whether levels of the endogenous peptide substance P (SP) would parallel and reflect the reported increased levels of the trophic agent nerve growth factor which is associated with the development of sympathetic hyperinnervation (and ultimately hypertension) in the genetic animal model for hypertension, the spontaneously hypertensive rat. / Thesis (Ph.D.)--University of Adelaide, Dept. of Clinical and Experimental Pharmacology, 1995

Includes bibliographical references (leaves 169-205). / xvii, 205, [33] leaves, [10] leaves of plates : ill. (some col.) ; 30 cm. / Title page, contents and abstract only. The complete thesis in print form is available from the University Library. / Suggests that the testicular macrophage exhibits characteristics similar to that of a suppressor macrophage phenotype. The inhibition of lymphocyte proliferation by the testicular macrophage, its unique cytokine profile, high basal production of GM-CSF and prostaglandins, and the refractoriness to LPS all suggests a role that contributes to the immune privilege that is afforded the testis. However, these aspects of testicular macrophage immuno-biology also support a role in local cell-cell communication and regulation of the normal physiology of the testis, and macrophages may be directly involved in Leydig cell steriogenesis. / Thesis (Ph.D.)--University of Adelaide, Dept. of Animal Science, 1997?

The molecular form distribution of adenosine deaminase has been characterized in nine rat tissues. This study has also investigated the effects of 70% partial hepatectomy in liver, spleen, and intestinal tissues. In all tissues studied, the molecular weight of the enzyme was found to be 35,000 daltons, as determined by gel filtration chromatography. Two prominent isozymes of this molecular weight were identified by means of thin-layer isoelectric focusing. Isozymes with pI's of 4.95 and 4.80 were present in tissues of liver, spleen, and intestine of normal and hepatectomised rats. Throughout the liver regeneration period, activity levels of adenosine deaminase were elevated in all tissues examined.Ball State UniversityMuncie, IN 47306

This study examined the effects of maintaining exercise training throughout pregnancy upon metabolic and physical properties of parametrial fat cells and fetal growth in Wistar rats. Eight weeks prior to mating the animals (n=10) were trained to run for 2 hrs/day, 5 days/wk at 31 m/min up an 8 0 incline. Control animals (n=6) remained sedentary. All animals were mated and trained animals resumed running on the second day of gestation. There was no variation in body weight (p > 0.05) between the trained (T) and sedentary control (S) rats at mating but S weight was significantly greater (p < 0.05) at Day 19. The T mothers had significantly smaller fat cells (p < 0.05) than S but cell number did not differ (p > 0.05). The rate of glucose oxidation (1C-1) by cells from T animals was significantly higher (p < 0.05) than the S in the presence of insulin, but much lower than oxidation rates of non-pregnant trained animals. In terms of the fetus, training reduced litter size (p < 0.05) and increased the incidence of fetal resorption. The results of this study indicate that the training adaptation of the adipocytes is largely lost during pregnancy but insulin responsiveness is maintained at a higher level than sedentary controls. This coupled with the apparent adverse effects of the training on the fetus suggests that exercise during pregnancy should be more closely investigated.Ball State UniversityMuncie, IN 47306

The effects of an 8-week swim training program and a 3-week detraining period on the size and protein composition of the heart of female Wistar rats were examined. The animals were separated into three groups: trained, detrained, and sedentary control. The training program, 6 hours/day, 5 days/week, resulted in a significantly larger dry heart weight, a normal collagen concentration, and a nonsignificantly greater total protein content. The greatest changes occurred between 4 and 6 weeks of training. The mild physiologic hypertrophy was assumed to be typical, and therefore simply an enlargement of a normal heart with proportional increases in myocyte size, and connective and vascular tissue hyperplasia. The detraining period produced a return of the heart mass to normal by the end of 2 weeks of detraining. The total protein content and collagen concentration remained elevated, though nonsignificant. The results indicate the detrained heart is composed of more connective, vascular, and metabolically active tissue, all of which may be important in the detrained heart’s response to increased work.Ball State UniversityMuncie, IN 47306

This study was done to examine the effects of detraining upon the metabolism of glucose by the rats. Thirty-nine female Wister rats were separated into three groups: trained, detrained, and sedentary. The training protocol consisted of swimming 6 hours/day for eight weeks. The detrained groups were then sacrificed at 7, 14, and 21 days after training. The parametrial fat pads were removed and digested into isolated cells. The cell volumes, cell concentrations, and glucose oxidation rates (radioactively labeled C-1 or C-6 glucose) were measured. The results showed that those adaptations in the fat cell brought about by exercise, i.e., 120% decreases adipocyte volume and increased glucose oxidation rates in both pentose phosphate (C-1) cycle and the glycolysis/citric acid cycles, return to the sedentary control levels by 14 days detraining.Ball State UniversityMuncie, IN 47306

The purpose of this study was to examine the effect of glucose ingestion on glycogen use andresynthesis during moderate exercise in untrained rats. Female Wistar rats (avg. wt.= 262 g) were assigned to either a control (C), control exercise (CE) or experimental exercise (EE) group. To examine glycogen resynthesis during exercise from a carbohydrate feeding, the EE animals were given 1 ml of a 10% glucose solution enriched with U-14C-glucose via stomach tube and run for 1h at 20.6 m/min. To distinguish between glycogen synthesis from endogenous versus exogenous sources, the CE animals were given a 0.1 ml tail-vein injection of U-14C-glucose tracer and run for 1h at 20.6 m/min. The C animals served as resting controls. Immediately after sacrifice, samples of the liver, soleus m., plantaris m., gastrocnemius m. and w. vastus m. were removed and analyzed for glycogen concentration and 14C activity in a glycogen pellet. Muscle and liver glycogen was 4.72 umol/g and 5.16 umol/g, respectively, higher (p<0.05) in the EE animals than in the CE animals. The average 14C activity of the muscle glycogen (mean ± SE) (182.85+ 31.79 cpm/g) was greater (p<0.05) than that of the liver (47.44 + 8.10 cpm/g), indicating a greater exogenous glucose incorporation into muscle glycogen than liver glycogen during exercise. However, this activity represented less than 2% of the remaining glycogen found in each tissue. Thus, it appears that the glycogen sparing observed with the glucose feeding in untrained rats was the result of an increased contribution of blood glucose to muscle metabolism.Ball State UniversityMuncie, IN 47306

Forty Sprague Dawley rats were randomly separated into one of three experimental groups: Run-Trained (RT), Swim-Trained (SW), or Control (CON). The runners were further separated into 2 groups: Good-runners (RT1), or Poor-runners (RT2) according to their performance on the treadmill. All of the trained groups were endurance trained at approximately 80% V02 max for two hours per day, five days per week in the appropriate mode of exercise. After nine weeks of equi-intensity training, the perimetrial fat pads were removed and the calls isolated. The adipocytes from the trained animals were significantly smaller in volume and diameter than the adipocytes from the controls. Adipocytes from all of the trained groups were significantly more sensitive to insulin than the CON group according to the definition by Kahn (60). The cells from the RT1 and SW groups were significantly more responsive to insulin than both the RT2 and CON groups. The adipocytes from the RT1 group were also significantly more responsive to insulin than the SW group. The differences in cell responsiveness to insulin were highly correlated to the average size of the cells studied. From the data presented in this study threeconclusions were drawn: 1) Both running and swimming at the reported intensity, duration, and frequency have a significant effect on the morphology and metabolism of the isolated adipocyte, 2) Adipocyte morphology, insulin sensitivity, and insulin responsiveness are dependent on the frequency, intensity, and duration of a given exercise training protocol, and 3) Each type of exercise training has its own drawbacks: with swimming, the rats may experience some hypoxia which may alter their metabolic fuel utilization, and during running not all of the animals may be capable or willing to complete the run.Ball State UniversityMuncie, IN 47306

published_or_final_version / Pharmacology and Pharmacy / Doctoral / Doctor of Philosophy

published_or_final_version / Physiology / Master / Master of Medical Sciences