Lavyne M H, Hariri R J, Tankosic T, Babiak T
Neurosurgery. 1983 Apr;12(4):430-4. doi: 10.1227/00006123-198304000-00010.
Low dose gamma-butyrolactone (GBL) therapy alters the natural history of experimental forebrain ischemia in the awake rat. After 30 minutes of four-vessel ischemia, repeated hydrogen cerebral blood flow determinations in awake rats over 72 hours revealed that low dose GBL therapy prevented the development of regional cerebral hyperemia and later the prolonged cerebral hypoperfusion that was experienced by the nontreated controls. Moreover, the low dose GBL-treated group had significantly less neuronal tissue loss than that in comparable brain regions of the nontreated controls. Before the stroke studies, GBL dose-response experiments performed on normal rats indicated that high dose GBL therapy produced seizures, systemic hypertension, metabolic acidosis, hyperthermia, and death.
低剂量γ-丁内酯(GBL)疗法可改变清醒大鼠实验性前脑缺血的自然病程。在进行30分钟的四血管缺血后,对清醒大鼠在72小时内反复进行脑血流测定,结果显示低剂量GBL疗法可预防局部脑充血的发展,以及随后未治疗对照组所经历的长时间脑灌注不足。此外,低剂量GBL治疗组的神经元组织损失明显少于未治疗对照组的相应脑区。在进行中风研究之前,对正常大鼠进行的GBL剂量反应实验表明,高剂量GBL疗法会导致癫痫发作、系统性高血压、代谢性酸中毒、体温过高和死亡。