Our laboratory has developed a method which enables us to quantitate 6 different forms of renin secreted by renal cortical slices. Each form has a different isoelectric point but similar molecular weight. We are also able to incorporate H3 labelled leucine into the renin molecule. Using these techniques we plan to study two general problems. The first is concerned with the number and nature of the different cellular pools for renin. We are able to show that isoproterenol stimulation and low salt diets stimulate kidneys to release different renin profiles. It appears that distinct pools of renin, each having a unique subset of renin forms respond to different stimuli. We hope to characterize these pools better; to determine which physiological events stimulate which subset. Conversely we hope to characterize those pools which are inhibited by ADH and angiotensin. All experiments will involve measurement of the renin forms secreted by renal cortical slices and perfused kidneys before and after stimulation and inhibition.
The second aim i s to quantify the partitioning of newly formed renin into stored and secreted renin. By labelling slices with H3 leucine we should be able to time the movement of the newly synthetized renin into storage pools and into the secreted fractions.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL031946-02
Application #
3343132
Study Section
Cardiovascular and Pulmonary Research B Study Section (CVB)
Project Start
1984-05-01
Project End
1987-04-30
Budget Start
1985-05-01
Budget End
1986-04-30
Support Year
2
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Type
Schools of Medicine
DUNS #
791277940
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Malvin, R L; Chen, M; Lloyd, M C (1989) Functional relevance of the microheterogeneity of active renin. Am J Hypertens 2:414-8
Kim, S H; Lloyd, M C; Sessler, F M et al. (1988) Functional differences of six forms of renin in rats. Am J Physiol 254:F432-9
Harker, C T; Kluger, M J; Malvin, R L (1987) Temperature sensitivity of renin-angiotensin system in the ground squirrel. Am J Physiol 253:F471-5
Beasley, D; Shier, D N; Malvin, R L et al. (1986) Angiotensin-stimulated drinking in marine fish. Am J Physiol 250:R1034-8
Sessler, F M; Kim, S H; Malvin, R L (1986) Changes of renin isoelectric heterogeneity after acute and chronic stimulation of renin secretion. Proc Soc Exp Biol Med 182:258-62
Sessler, F M; Jokelainen, P T; Sing, C F et al. (1986) Renin heterogeneity in stroke-prone hypertensive and normotensive rats. Am J Physiol 251:E367-72
Sessler, F M; Jacquez, J A; Malvin, R L (1986) Different production and decay rates of six renin forms isolated from rat plasma. Am J Physiol 250:E551-7
Shier, D N; Malvin, R L (1985) Differential secretion and removal of multiple renin forms. Am J Physiol 249:R79-84