Grants and Contracts Details
Description
Abstract:
Hypoglycemia is the most prevalent clinical complication in the daily management of diabetes and is
the major obstacle to normalizing blood sugar. For people with Type 1 diabetes (T1DM), hypoglycemia
associated autonomic failure (HAAF) increases the risk for severe hypoglycemia by a factor of 25 or more. A
major component of HAAF is hypoglycemia unawareness, which involves in the loss/diminution of warning
symptoms to hypoglycemia that would normally prompt a corrective behavioral response (e.g., eating food).
With a goal of identifying existing biological compounds that could restore hypoglycemia awareness (ie,
repurpose existing FDA- approved drugs), our laboratory recently completed a drug screen using a novel
animal model of hypoglycemia unawareness in which preconditioned rats failed to increase food consumption
in response to an episode of insulin induced hypoglycemia. Of all drugs tested, the dopamine antagonist
metoclopramide consistently restored hypoglycemia awareness in several of our animal models tested. The
goal of Aim 1 in the proposed grant is to validate in T1DM animal models of HAAF whether leading drugs
identified in our recent drug screen restore both,
1) hypoglycemia awareness, and 2) the impaired sympathoadrenal response to hypoglycemia. Utilizing the
gold standard hyperinsulinemic hypoglycemic clamp technique, drug validation studies are proposed in two
independent T1DM rodent models of HAAF (both hypoglycemia unaware rats as well rats with recurrent
hypoglycemia-induced sympathoadrenal deficiency) to determine if treatment with our leading drugs reverse
these two principal pathologic components of HAAF. In Aim 2, a clinical trial is proposed to test whether the
lead compound identified in our drug screen can restore both hypoglycemia awareness and the
counterregulatory response to hypoglycemia in subjects with T1DM and HAAF. A placebo controlled,
randomized trial will test whether four weeks of treatment with metoclopramide (our lead drug noted to
particularly efficacious in several preclinical models) will, 1) reduce the incidence of hypoglycemia, 2)
improve hypoglycemia symptom recognition, and 3) improve the sympathoadrenal response to
hypoglycemia. Indices of improvement will be assessed, 1) in the outpatient setting with hypoglycemia event
diaries, hypoglycemia awareness questionnaires, and continuous glucose monitors, and 2) in the laboratory
setting with stepped hypoglycemic clamps which quantifies measurements of symptomatic awareness and
counterregulatory hormone responses. By proceeding forward with the novel results from our recent drug
screen, the proposed studies are the logical next step in seeking to repurpose existing FDA approved drugs
to treat hypoglycemia associated autonomic failure in people with Type 1 diabetes.
Status | Active |
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Effective start/end date | 4/1/19 → 3/31/25 |
Funding
- National Institute Diabetes & Digestive & Kidney: $1,116,851.00
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