No abstract available.
Licensure*

It is still not well documented what the basic roles for the regulation of renin secretion from the kidney take place. Since the early study on the renal ischemia for the production of hypertension was introduced, the renin-angiotensin system has been regarded as the possible pathogenetic mechanism for the renovascular hypertension. The renin-angiotensin system, however, could be activated by various stimuli, such as, the changes of intrarenal perfusion pressure, the load or concentriation of sodium at the sites of macular densa, the changes of the sympathetic nervous activity and the changes of potassium balance. To investigate the renin-angiotensin system and the influence of sympathetic nervous system on the regulation of renin secretion, the renovascular hypertension was induced in the dogs by constriction of unilateral renal artery, and the plasma renin activity was measured. The sodium load at the sites of macula densa was attained by furosemide, and then the activity of sympathetic nervous system was depressed by reserpine. The plasma renin activity was assayed by the method of Helmer and Cohn. By this bio-assay method, the plasma renin activity equivalent to 1 nanogram angiotensin-II can be measurable and the prepared plasma was found to have still vasopressor activity. The results observed in this experimental work are summarized as follows. 1. The blood pressure reached maximum on the 3rd postoperative day, and declined gradually to the level of preoperative day on the day of from the 6th to 12th day following constriction of renal artery. 3. The plasma renin activity was found to be well correlated with the increase of blood pressure, and then declined to its preoperative level with the reduction of blood pressure. It appears, therefore, that the renin-angiotensin system plays an important role in the pathogenesis of renovascular hypertension. 4. The urine flow rate in normal and reserpinized dogs was the same before administration of furosemide, but its rate was significantly increased in both groups after furosemide. The urine flow rate of reserpinized dogs, however, was significantly lower than that of the normal dogs during the first 5 minutes. 5. The urinary sodium excretion in normal and reserpinized dogs was significantly increased in both groups after administration of furosemide and there were no difference between the two groups. 6. The plasma renin activity of renal venous blood was significantly higher than that of femoral arterial blood in both groups before and after administration of furosemide. 7. The plasma renin activity of reserpinized dogs was significantly lower than that of normal dogs before administration of furosemide. After furosemide, however, the plasma renin activity was significantly increased in 30 minutes in both groups. This increase of plasma renin activity was less prominent in resepinized dogs than in normal. This results would suggest that the intrarenal mechanism regulating renin secretion also requires an intact sympathetic nervous system.
Animals ; Blood Pressure ; Constriction ; Dogs ; Furosemide ; Hypertension ; Hypertension, Renovascular ; Ischemia ; Kidney ; Perfusion ; Plasma ; Potassium ; Renal Artery ; Renin* ; Renin-Angiotensin System ; Reserpine ; Sodium ; Sympathetic Nervous System

No abstract available.
Breast Neoplasms* ; Breast*

No abstract available.
Cardiovascular Diseases* ; Insulin*

No abstract available.

No abstract available.
Urinary Bladder*

In this study, foot girth, instep girth, instep height, foot arch height, foot length, foot width, heel width and five length items in forepart foot were measured using chiefly the method of measurements with foot projected contours. 38 young women and 5 young men participated in this experiments. Two positions of the foot were taken in account : 1) normal position-when body weight is not supported by right foot 2) weight loading position-when body weight is supported by right foot. The following results were obtained. 1. The change rates of the men subjects show a more increased shapes in foot width and forepart foot length than in the change rates of the women subjects. 2. The changes of foot shape when body weight is supported by one foot, inside part of the foot size was increased with greater surfaces in women while the outside part of the foot size was increased with greater surfaces in men subjects.
Body Weight ; Female ; Foot* ; Heel ; Humans ; Male ; Methods

A study on the Aedes togoi to find out important biological and ecological factors as an efficient vector of filariasis, was carried out on Che-Ju Island for two years from 1968 though 1969. Results obtained are as followings: Geographical distribution of the mosquito breeding habitat was found to be extensive covering circular areas of about three km distance along the shore line. The main breeding sites were rockpools and smaller holes on rocks retaining tide and/or rain water with high larval density; water tanks, pots, and other artificial containers retaining only rain water around the houses located within the area with relatively low larval density. Species constitution of adult mosquitos collected in the study villages consisted largely of Aedes togoi with a range of 70-90 per cent by village. The pH of the breeding sites ranged from 5.0 to l0.0, and the chloride content from 0.01 to 28.75 (gm/l). More than fifty per cent of examined sites, however, had pH 5.6-6.5 and chloride content of less than 1.0 gm/1. The natural infection rate of A. togoi by filaria showed proportional relationships with microfilaria rates among the human population by area. Experimental infection of A. togoi by human and dog filaria demonstrated that this species is an efficient vector for both filaria species proved by natural infection as well as experimental infection. Susceptibility of both larva and adult of A. togoi to insecticide, DDT and dieldrin, showed considerable sensitivity in all villages tested.
parasitology-arthropoda ; vector ; Aedes togoi ; epidemiology ; filariasis ; Brugia malayi ; chloride

No abstract available.

No abstract available.
Hepatitis B virus* ; Hepatitis B* ; Hepatitis* ; Liver*