Harada K, Meller E, Goldstein M
New York University Medical Center, Neurochemistry Research Laboratories, NY 10016.
Eur J Pharmacol. 1990 Mar 13;188(2-3):123-8. doi: 10.1016/0922-4106(90)90047-2.
The effects of pertussis toxin (PTX) on synaptosomal tyrosine hydroxylase (TH) activity and on the inhibition of synaptosomal TH activity by apomorphine were investigated. Exposure of striatal synaptosomes to PTX does not affect basal- or forskolin-stimulated TH activity, but attenuates apomorphine-elicited inhibition of forskolin-stimulated synaptosomal TH activity. There is a good correlation between the attenuation of apomorphine-elicited inhibition of synaptosomal TH activity by PTX and (-)-sulpiride, suggesting that G proteins are involved in the dopamine (DA) autoreceptor-mediated regulation of the enzyme activity. The exposure of synaptosome to PTX results in a 40-50% inactivation of Gi and Go proteins, which is evident from the reduction of ADP ribosylation with [32P]NAD of the remaining G proteins following preincubation with the toxin. The present study also demonstrates that striatal synaptosomal preparations can be used for investigations of the molecular properties of nerve terminal DA autoreceptors.
研究了百日咳毒素(PTX)对突触体酪氨酸羟化酶(TH)活性以及阿扑吗啡对突触体TH活性抑制作用的影响。将纹状体突触体暴露于PTX并不影响基础或福斯高林刺激的TH活性,但会减弱阿扑吗啡引起的对福斯高林刺激的突触体TH活性的抑制作用。PTX和(-)-舒必利对阿扑吗啡引起的突触体TH活性抑制作用的减弱之间存在良好的相关性,这表明G蛋白参与了多巴胺(DA)自身受体介导的酶活性调节。将突触体暴露于PTX会导致Gi和Go蛋白40 - 50%的失活,这在用毒素预孵育后,通过剩余G蛋白与[32P]NAD的ADP核糖基化减少得以证明。本研究还表明,纹状体突触体制剂可用于研究神经末梢DA自身受体的分子特性。