Diabetes mellitus develops spontaneously in mature Macaca nigra. The earliest hormonal and islet morphological alterations can be identified and studied before development of the abnormal glycemic criteria characteristic of diabetes. Altered intraislet secretory cell interactions lead to hormonal changes. Normal control mechanisms will be delineated and aberrations in islet hormone responses assessed by perfusion of the pancreas with various secretagogues in monkeys of different metabolic states. The effectiveness of preventive therapy regimens will be assessed in monkeys in the stages before overt diabetes. One group will receive tolbutamide, another group will be given insulin injections, and the third group will receive no therapy. Effective therapy should prevent or delay changes in glucagon and insulin levels and secretion, islet morphological deterioration, amyloid deposition, glycemic changes and secondary complications. Islets in pancreatic biopsy sections taken from monkeys of varied metabolic states will be examined to quantify alterations in secretory cell numbers and amounts of amyloid. Antibody involvement in the amyloidotic islet lesion will be assessed. The hormonal and islet morphological changes preceding diabetes can be detected in Macaca nigra long before similar stages in human beings. Monkeys can be intensively monitored, experimentally manipulated, and effectiveness of therapy assessed in ways not possible with human beings. Relationships between the hormonal and morphological aspects of the islet lesion can be identified and correlated with each other and with the development of diabetes. Data from Macaca nigra will be useful in determining whether identification and treatment of the hormonal and metabolite abnormalities preceding glycemic changes could prevent overt diabetes and its complications in humans.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis, Diabetes, Digestive and Kidney Diseases (NIADDK)
Type
Research Project (R01)
Project #
5R01AM021982-06
Application #
3151423
Study Section
Pathology B Study Section (PTHB)
Project Start
1978-07-01
Project End
1987-12-31
Budget Start
1985-01-01
Budget End
1985-12-31
Support Year
6
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Oregon Regional Primate Research Center
Department
Type
DUNS #
City
Beaverton
State
OR
Country
United States
Zip Code
97006
Howard Jr, C F; Yasuda, M; Wolff, J (1990) Hyperinsulinemia in Macaca nigra: precession to obesity and/or diabetes? Diabetes Res 13:163-8
Howard Jr, C F; Wolff, J; Van Bueren, A (1987) Lipoprotein patterns in nondiabetic, borderline diabetic, and diabetic Macaca nigra. Atherosclerosis 63:75-84
Beatty, C H; Baughman, W L; Caruso, V et al. (1986) Effects of intravenous epinephrine on macaque platelets. J Med Primatol 15:49-61
Fang, T Y; Howard Jr, C F (1986) Immunohistochemical study of islet amyloid in diabetes mellitus. Pancreas 1:293-300
Beatty, C H; Howard Jr, C F; Caruso, V (1986) Potentiation with epinephrine of macaque platelet aggregation by other agonists: implications for studies on human atherosclerosis. Thromb Res 41:447-58
Howard Jr, C F; Van Bueren, A (1986) Changes in islet cell composition during development of diabetes in Macaca nigra. Diabetes 35:165-71
Beatty, C H; Howard Jr, C F; Caruso, V (1986) Effects of ADP and epinephrine on macaque and human platelets. Implications for studies on human atherosclerosis. Atherosclerosis 60:111-8
Howard Jr, C F (1986) Longitudinal studies on the development of diabetes in individual Macaca nigra. Diabetologia 29:301-6
Beatty, C H; Howard Jr, C F; Hoskins, M K et al. (1985) Metabolism of arachidonic acid by macaque platelets. Implications for studies on atherosclerosis. Atherosclerosis 55:1-13
Howard, C F (1985) Atherosclerosis and insulin in primates with diabetes mellitus. Metabolism 34:60-6

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