Kramer E, Sperber E S, Bodnar R J
Physiol Behav. 1985 Dec;35(6):929-34. doi: 10.1016/0031-9384(85)90261-6.
Among the compromised physiological responses affected by aging is an impaired response to glucose. Since administration of 2-deoxy-D-glucose (2DG) produces both analgesic and hyperphagic responses in young adult rats, the present study examined whether systematic variations in these responses occurred as a function of age. Separate cohorts of 4, 9, 14, 19 and 24 month old female rats received ascending doses of 2DG (0, 50, 250, 450, 650 mg/kg) with tail-flick latencies and jump thresholds assessed 30, 60 and 120 min later. Then the same rats received 2DG injections (0, 650, 1200 mg/kg) and food intake was assessed 5 hr later. Significant decreases in 2DG analgesia were observed on the tail-flick test as a function of age with the maximal decrease observed at the highest 2DG dose. Significant decreases in 2DG analgesia were generally observed on the jump test as a function of age, although this effect was not as robust as that observed on the tail-flick test. Finally, significant and systematic decreases in 2DG hyperphagia were observed as a function of age following both the 650 mg/kg and the 1200 mg/kg doses. The observed decrements in the analgesic and hyperphagic responses to 2DG as a function of age appear to represent an orderly alteration in responses to glucoprivation through adulthood.
衰老所影响的生理反应中,对葡萄糖的反应受损是其中之一。由于给予2-脱氧-D-葡萄糖(2DG)会在成年幼鼠中产生镇痛和摄食亢进反应,本研究探讨了这些反应的系统性变化是否随年龄而发生。将4、9、14、19和24月龄的雌性大鼠分为不同队列,给予递增剂量的2DG(0、50、250、450、650mg/kg),并在30、60和120分钟后评估甩尾潜伏期和跳跃阈值。然后,对相同的大鼠注射2DG(0、650、1200mg/kg),并在5小时后评估食物摄入量。在甩尾试验中,观察到2DG镇痛作用随年龄显著降低,在最高2DG剂量时下降最大。在跳跃试验中,一般也观察到2DG镇痛作用随年龄显著降低,尽管这种效应不如在甩尾试验中观察到的那样明显。最后,在650mg/kg和1200mg/kg剂量后,观察到2DG引起的摄食亢进随年龄显著且系统性地降低。观察到的2DG镇痛和摄食亢进反应随年龄的下降似乎代表了成年期对糖剥夺反应的有序改变。