Effects of d-3-hydroxybutyrate treatment on hypoglycemic coma in rat pups

详细信息    查看全文

• 作者：Peter W. Schutz^a ; ^b ; ^{schutz@interchange.ubc.ca} ; Peter K.H. Wong^a ; ^c ; John O'Kusky^b ; Sheila M. Innis^d ; Sylvia Stockler^a
• 关键词：Ketone bodies ; Neuroprotection ; Hypoglycorrhachia ; Neuroglycopenia
• 刊名：Experimental Neurology
• 出版年：2011
• 出版时间：January 2011
• 年：2011
• 卷：227
• 期：1
• 页码：180-187
• 全文大小：907 K

文摘

d-3-Hydroxybutyrate (3OHB) is an alternative energy substrate for the brain during hypoglycemia, especially in infancy. Knowledge of the capacity and limits of 3OHB to compensate for cerebral glucose depletion during hypoglycemia in developing brain is important for its potential clinical use, but is scarce. We studied the effect of 3OHB treatment during insulin-induced hypoglycemia in 13-day-old rat pups. 3OHB treatment resulted in increased 3OHB plasma levels in hypoglycemic animals (3–4 mM vs. 0.5–1 mM untreated), and delayed the onset of clinical coma by 70 min and of burst-suppression coma by 90 min. 3OHB treated animals did not survive after resuscitation with glucose, compared to 80 % survival of untreated hypoglycemic pups. Cleaved-caspase-3 immunohistochemistry and double labeling studies demonstrated a 20-fold increase of apoptotic mature oligodendrocytes in white matter of 3OHB treated animals. 3OHB treatment delays the onset of clinical and burst-suppression coma during hypoglycemia, but the prolonged duration of hypoglycemia is associated with increased mortality after resuscitation and cellular white matter injury.