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犬全脑缺血后糖尿病慢性高血糖与脑pH值恢复

Diabetic chronic hyperglycemia and cerebral pH recovery following global ischemia in dogs.

作者信息

Sieber F E, Koehler R C, Brown P R, Eleff S M, Traystman R J

机构信息

Department of Anesthesiology/Critical Care Medicine, Johns Hopkins University, Baltimore, Md.

出版信息

Stroke. 1994 Jul;25(7):1449-55. doi: 10.1161/01.str.25.7.1449.

Abstract

BACKGROUND AND PURPOSE

We determined the effect of chronic hyperglycemia associated with diabetes on recovery of cerebral pH after global incomplete cerebral ischemia.

METHODS

31P magnetic resonance spectra and cerebral blood flow (radiolabeled microspheres) were measured in three groups of dogs: (1) chronic hyperglycemic diabetes (pancreatectomy followed by blood glucose > 10 mmol/L for 3 months; n = 8); (2) acute hyperglycemia during ischemia and reperfusion in nondiabetic dogs (n = 8); and (3) normoglycemic controls (n = 8). Incomplete ischemia was produced for 20 minutes by ventricular fluid infusion followed by 3 hours of reperfusion.

RESULTS

Cerebral blood flow was reduced to approximately 5 mL/min per 100 g in all groups during ischemia with individual values ranging from 1 to 11 mL/min per 100 g. Blood flow returned to preischemic values by 30 minutes of reperfusion in the normoglycemia group but remained elevated during reperfusion in the acute hyperglycemia and diabetes groups. Cerebral pH at the end of ischemia was lower in acute hyperglycemia (5.94 +/- 0.05; +/- SE) and diabetes (5.97 +/- 0.08) groups than in the normoglycemia group (6.27 +/- 0.02). However, recovery of pH through 90 minutes of reperfusion in the normoglycemia (7.08 +/- 0.05) and diabetes (7.00 +/- 0.04) groups was significantly greater than in the acute hyperglycemia group (6.74 +/- 0.11). Persistent acidosis in the acute hyperglycemia group was associated with a delayed reduction of cerebral oxygen consumption and high-energy phosphates and with greater cortical water content and impairment of somatosensory evoked potentials compared with the diabetes group.

CONCLUSIONS

This study shows that cerebral pH recovery after global incomplete ischemia is improved in chronic hyperglycemia compared with acute hyperglycemia, despite similar decreases in blood flow and pH during ischemia and similar levels of blood flow and glucose levels during ischemia and reperfusion. In addition, cerebral pH recovery in chronic hyperglycemic dogs was not different from that in normoglycemic controls. These results suggest that an adaptation occurs with chronic hyperglycemia that improves recovery of cerebral pH during reperfusion and that is associated with better maintenance of energy metabolism and evoked potentials and with less edema over 3 hours of reperfusion compared with acute hyperglycemia.

摘要

背景与目的

我们确定了与糖尿病相关的慢性高血糖对全脑不完全缺血后脑pH值恢复的影响。

方法

对三组犬进行³¹P磁共振波谱和脑血流量(放射性微球)测量:(1)慢性高血糖糖尿病组(胰腺切除术后血糖>10 mmol/L持续3个月;n = 8);(2)非糖尿病犬在缺血和再灌注期间的急性高血糖组(n = 8);(3)正常血糖对照组(n = 8)。通过脑室灌注20分钟造成不完全缺血,随后进行3小时再灌注。

结果

在缺血期间,所有组的脑血流量均降至约每100 g每分钟5 mL,个体值范围为每100 g每分钟1至11 mL。正常血糖组在再灌注30分钟时血流恢复到缺血前值,但急性高血糖组和糖尿病组在再灌注期间血流仍升高。急性高血糖组(5.94±0.05;±标准误)和糖尿病组(5.97±0.08)在缺血结束时的脑pH值低于正常血糖组(6.27±0.02)。然而,正常血糖组(7.08±0.05)和糖尿病组(7.00±0.04)在90分钟再灌注期间的pH值恢复明显大于急性高血糖组(6.74±0.11)。与糖尿病组相比,急性高血糖组持续酸中毒与脑氧消耗和高能磷酸盐延迟降低、皮质含水量增加以及体感诱发电位受损有关。

结论

本研究表明,与急性高血糖相比,慢性高血糖时全脑不完全缺血后脑pH值恢复得到改善,尽管缺血期间血流和pH值下降相似,且缺血和再灌注期间血流和血糖水平相当。此外,慢性高血糖犬的脑pH值恢复与正常血糖对照组无差异。这些结果表明,慢性高血糖会发生一种适应性变化,可改善再灌注期间脑pH值的恢复,与急性高血糖相比,在3小时再灌注期间与更好地维持能量代谢和诱发电位以及更少的水肿有关。

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