EFFECT OF SULFONYLUREA THERAPY ON PLASMA-INSULIN, INTACT AND 32 33 SPLIT PROINSULIN IN SUBJECTS WITH TYPE-2 DIABETES-MELLITUS

被引:33
作者
DAVIES, MJ
METCALFE, J
DAY, JL
GRENFELL, A
HALES, CN
GRAY, IP
机构
[1] Ipswich Diabetes Centre, Ipswich Hospital
[2] Central Middlesex Hospital, London
[3] Department of Clinical Biochemistry, Addenbrookes Hospital, Cambridge
[4] St Mary's Hospital, London
关键词
TYPE-2; DIABETES-MELLITUS; SULFONYLUREA; INSULIN; PROINSULIN;
D O I
10.1111/j.1464-5491.1994.tb00274.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
This study was undertaken to clarify the effect of sulphonylurea therapy on beta cell function in 27 subjects with newly diagnosed Type 2 diabetes mellitus. Plasma glucose, insulin, intact and 32/33 split proinsulin were measured at diagnostic OGTT. After 8-12 weeks on a conventional diet, subjects with a fasting glucose > 9 mmol l-1 (n = 12) were commenced on sulphonylurea therapy. At diagnosis, the sulphonylurea requiring group were more hyperglycaemic (p < 0.0001), less obese (p < 0.05) and more insulin deficient with a lower 30 min insulin (p < 0.0002) than the diet group. Following dietary intervention in the sulphonylurea group, weight remained unchanged but there was a reduction in fasting glucose (p < 0.009). Fasting insulin, intact proinsulin, and 32/33 split proinsulin remained unchanged. After 12 weeks of sulphonylurea therapy there was a weight gain of 1.5 kg (p < 0.01), but a reduction in fasting glucose (p < 0.0001). Fasting insulin and intact proinsulin increased (p < 0.004) but 32/33 split proinsulin remained unchanged. There was a significant increase in both the fasting insulin to glucose ratio (p < 0.005), and the intact to 32/33 split proinsulin ratio (p < 0.02). Final fasting glucose following sulphonylurea therapy was positively correlated with the initial intact and 32/33 split proinsulin and the fasting glucose following dietary treatment. It is clear from this work that sulphonylureas have a complex effect on beta cell physiology and as well as stimulating release of insulin they increase the release of intact proinsulin but not that of 32/33 split proinsulin, hence they increase the intact to 32/33 split proinsulin ratio.
引用
收藏
页码:293 / 298
页数:6
相关论文
共 33 条
[21]  
Cerasi E., Efendic S., Thornqvist C., Luft R., Effect of two sulphonylureas on the dose kinetics of glucose‐induced insulin release in normal and diabetic subjects, Acta Endocrinol, 91, pp. 282-293, (1979)
[22]  
Unger RH, Grundy S., Hyperglycaemia as an inducer as well as a consequence of impaired islet cell function and insulin resistance: implications for the management of diabetes, Diabetologia, 28, pp. 119-121, (1985)
[23]  
Davies M., Alban-Davies H., Cook C., Day J., Self testing for diabetes mellitus, Br Med J, 303, pp. 696-698, (1991)
[24]  
(1985)
[25]  
Sobey WJ, Beer SF, Carrington CA, Clark PMS, Frank BH, Gray IP, Et al., Sensitive and specific and two‐site immunoradiometric assays for human insulin, proinsulin, 65–66 split and 32–33 split proinsulins, Biochem. J., 260, pp. 535-541, (1989)
[26]  
Davies MJ, Grenfell A., Metcalfe J., Gray IP, Day JL, Hales CN., Improved beta cell function following dietary treatment in non‐insulin‐dependent diabetes mellitus (NIDDM) (Abstract), Diabetic Med, 9, (1992)
[27]  
Yoshioka N., Kuzuya T., Matsuda A., Iwamoto Y., Effects of dietary treatment on serum insulin and proinsulin response in newly diagnosed NIDDM, Diabetes, 38, pp. 262-266, (1989)
[28]  
Hales CN, Barker DJP., Type 2 (non‐insulin‐dependent) diabetes mellitus: the thrifty phenotype hypothesis, Diabetologia, 35, pp. 595-601, (1992)
[29]  
Peavy DE, Brunner MR, Duckworth WC, Hooker CS, Frank BH., Receptor binding and biological potency of several split forms (conversion intermediates) of human proinsulin: studies in cultured IM9 lymphocytes and in vivo and in vitro in rats, J Biol Chem, 260, pp. 13989-13994, (1985)
[30]  
Bennett DL, Bailyes EM, Hutton JC., Immunological identification of the type 2 proinsulin endopeptidase as the subtilsin‐like protein PC2 (Abstract), Diabetic Med, 8, (1991)