Physiological responses during hypoglycaemia induced by regular human insulin or a novel human analogue, insulin glargine

Abstract

SUMMARY Aim Glargine, a product of recombinant technology, has different structural and physico‐chemical properties compared with native human insulin. We determined whether such differences are associated with alterations in the responses to hypoglycaemia induced by glargine. Methods Nineteen adults (six healthy and 13 with type 1 diabetes) underwent a 5‐h hyperinsulinaemic (2 mU/kg/min −1 ) stepped hypoglycaemic clamps (hourly targets of 4.7, 4.2, 3.6, 3.1 and 2.5 mmol/l, respectively) on two occasions using intravenous infusion of regular human insulin or glargine, in random sequence. Hypoglycaemic symptoms, counter‐regulatory hormones and glucose disposal rates were assessed at intervals throughout the clamps. A 1‐week ‘wash out’ period was observed between studies. Results The peak total symptoms scores (mean ± s.e.m.) at nadir blood glucose (2.5 mmol/l) were 18.83 ± 2.68 (healthy) and 17.46 ± 3.62 (diabetic) during regular insulin, and 18.50 ± 3.20 (healthy) and 19.08 ± 3.83 (diabetic) during glargine infusion. The peak epinephrine levels during hypoglycaemia were 767.8 ± 140.4 pg/ml (regular insulin) and 608.8 ± 129.9 pg/ml (glargine) among healthy subjects, and 332.5 ± 54.8 pg/ml (regular insulin) and 321.8 ± 67.4 pg/ml (glargine) in diabetic patients. Diabetic patients had blunted glucagon responses during hypoglycaemia with either insulin. Both insulins also elicited similar rates of glucose disposal. Conclusions We conclude that insulin glargine and regular human insulin elicit comparable symptomatic and counter‐regulatory hormonal responses during hypoglycaemia in healthy or diabetic subjects, and induce similar rates of glucose disposal. Since glargine is designed for subcutaneous (s.c.) use, it is possible (though unlikely) that our findings obtained using an intravenous protocol could differ from responses to hypoglycaemia induced by the s.c. route.