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Antecedent glycemic control reduces severe hypoglycemia-induced neuronal damage in diabetic rats.

  • Candace M. Reno
  • , Tariq Tanoli
  • , Adam Bree
  • , Dorit Daphna-Iken
  • , Chen Cui
  • , Susan E. Maloney
  • , David F. Wozniak
  • , Simon J. Fisher

Producción científica: Articlerevisión exhaustiva

22 Citas (Scopus)

Resumen

Brain damage due to severe hypoglycemia occurs in insulin-treated people with diabetes. This study tests the hypothesis that chronic insulin therapy that normalizes elevated blood glucose in diabetic rats would be neuroprotective against brain damage induced by an acute episode of severe hypoglycemia. Male Sprague-Dawley rats were split into three groups: 1) control, non-diabetic; 2) STZ-diabetic; and 3) insulin-treated STZ-diabetic. After 3 wk of chronic treatment, unrestrained awake rats underwent acute hyperinsulinemic severe hypoglycemic (10-15 mg/dl) clamps for 1 h. Rats were subsequently analyzed for brain damage and cognitive function. Severe hypoglycemia induced 15-fold more neuronal damage in STZ-diabetic rats compared with nondiabetic rats. Chronic insulin treatment of diabetic rats, which nearly normalized glucose levels, markedly reduced neuronal damage induced by severe hypoglycemia. Fortunately, no cognitive defects associated with the hypoglycemia-induced brain damage were observed in any group. In conclusion, antecedent blood glucose control represents a major modifiable therapeutic intervention that can afford diabetic subjects neuroprotection against severe hypoglycemia-induced brain damage.

Idioma originalEnglish
Páginas (desde-hasta)E1331-1337
PublicaciónAmerican Journal of Physiology - Endocrinology and Metabolism
Volumen304
N.º12
DOI
EstadoPublished - jun 15 2013

Financiación

FinanciadoresNúmero del financiador
National Institute of Neurological Disorders and StrokeP30NS057105

    ODS de las Naciones Unidas

    Este resultado contribuye a los siguientes Objetivos de Desarrollo Sostenible

    1. Good health and well being
      Good health and well being

    ASJC Scopus subject areas

    • Endocrinology, Diabetes and Metabolism
    • Physiology
    • Physiology (medical)

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