Rakovska A
Institute of Physiology, Bulgarian Academy of Sciences, Sofia, Bulgaria.
Neuropeptides. 1995 Nov;29(5):257-62. doi: 10.1016/0143-4179(95)90034-9.
The release of [3H]gamma-aminobutyric acid ([3H]GABA) from rat striatal slices before and during electrical field stimulation (EFS) was measured. Electrical stimulation (10 Hz) induced an increase of Ca(++)- and tetrodotoxin-sensitive [3H]GABA release from the striatal slices. In the presence of sulphated octapeptide of cholecystokinin, CCK-8S (10(-9) M, 10(-8) M and 10(-7) M) both the basal and the electrically (10 Hz)-evoked release of [3H]GABA were dose-dependently increased. These effects of CCK-8S were abolished by tetrodotoxin (10(-6) M) and were not influenced by the CCK-A receptor antagonist loxiglumide (CR1505) (10(-7) M and 10(-6) M). The stimulant effect of CCK-8S was antagonized by the newly synthesized CCK-B selective receptor antagonist PD134308 (10(-7) M and 10(-6) M). These findings suggest that CCK-8 plays a neuromodulatory role in the regulation of GABAergic neuronal activity in the striatum. The activation of CCK-B receptors located on GABAergic neurons is involved in the GABA release-potentiating effect of CCK-8S in rat striatum.
在电场刺激(EFS)之前和期间,对大鼠纹状体切片中[3H]γ-氨基丁酸([3H]GABA)的释放进行了测量。电刺激(10Hz)诱导纹状体切片中Ca(++)和河豚毒素敏感的[3H]GABA释放增加。在存在胆囊收缩素的硫酸化八肽CCK-8S(10^(-9)M、10^(-8)M和10^(-7)M)的情况下,[3H]GABA的基础释放和电刺激(10Hz)诱发的释放均呈剂量依赖性增加。CCK-8S的这些作用被河豚毒素(10^(-6)M)消除,且不受CCK-A受体拮抗剂洛西格列肽(CR1505)(10^(-7)M和10^(-6)M)的影响。新合成的CCK-B选择性受体拮抗剂PD134308(10^(-7)M和10^(-6)M)拮抗了CCK-8S的刺激作用。这些发现表明,CCK-8在纹状体中GABA能神经元活动的调节中起神经调节作用。位于GABA能神经元上的CCK-B受体的激活参与了CCK-8S在大鼠纹状体中增强GABA释放的作用。