Nalepa I, Pintor A, Chalecka-Franaszek E, Fortuna S, Michalek H, Vetulani J
Laboratory of Pharmacology, Istituto Superiore di Sanità, Rome, Italy.
Neurochem Res. 1993 May;18(5):585-9. doi: 10.1007/BF00966935.
The effects of glutamate, NMDA and quisqualate on carbachol- and norepinephrine-elicited formation of inositol phosphate (IP) were evaluated in slices prepared from the cerebral cortex of 3- and 24-month Sprague-Dawley rats. Glutamate, NMDA, and quisqualate antagonized the IP response to carbachol in a concentration-dependent fashion. This antagonism was more pronounced in aged than in young rats, both for glutamate (IC5O 0.114 and 0.210 mM) and NMDA (IC5O 0.0029 and 0.127 mM), but not for quisqualate. Glutamate (but not NMDA) also antagonized in a concentration-dependent fashion the IP response to norepinephrine, IC50s were 0.061 and 0.126 mM for aged and young rats, respectively; quisqualate had an inhibitory effect only at 1 mM concentration in the two age-groups, while in aged rats some stimulatory effect was present at 0.1 mM concentration. Glutamate, NMDA and quisqualate (1 mM) did not affect basal IP accumulation in either young or aged rats; quisqualate, however, at 0.1 mM concentration had some stimulatory effect, more pronounced in aged rats. This effect was probably responsible for the biphasic effect of quisqualate in this age-group. The most important finding consists of the demonstration of an age-related increase in the inhibitory effects of NMDA on carbachol-induced IP accumulation. This implies an altered modulation of cholinergic post-receptor mechanisms by glutamatergic mechanisms.
在3个月和24个月大的Sprague-Dawley大鼠大脑皮层制备的切片中,评估了谷氨酸、N-甲基-D-天冬氨酸(NMDA)和喹啉酸对卡巴胆碱和去甲肾上腺素引发的肌醇磷酸(IP)形成的影响。谷氨酸、NMDA和喹啉酸以浓度依赖的方式拮抗IP对卡巴胆碱的反应。这种拮抗作用在老年大鼠中比在年轻大鼠中更明显,无论是谷氨酸(IC50分别为0.114和0.210 mM)还是NMDA(IC50分别为0.0029和0.127 mM),但喹啉酸并非如此。谷氨酸(而非NMDA)也以浓度依赖的方式拮抗IP对去甲肾上腺素的反应,老年和年轻大鼠的IC50分别为0.061和0.126 mM;喹啉酸仅在两个年龄组中1 mM浓度时有抑制作用,而在老年大鼠中0.1 mM浓度时有一些刺激作用。谷氨酸、NMDA和喹啉酸(1 mM)对年轻或老年大鼠的基础IP积累均无影响;然而,喹啉酸在0.1 mM浓度时有一些刺激作用,在老年大鼠中更明显。这种作用可能是该年龄组中喹啉酸双相作用的原因。最重要的发现是证明了NMDA对卡巴胆碱诱导的IP积累的抑制作用存在与年龄相关的增加。这意味着谷氨酸能机制对胆碱能受体后机制的调节发生了改变。