Pinna A, Di Chiara G
Department of Toxicology, University of Cagliari, Italy.
Behav Pharmacol. 1998 Feb;9(1):15-21.
In unilaterally 6-hydroxydopamine lesioned rats the ability of two non-peptide delta-opioid agonists, BW 373U86 and SNC 80, to induce motor asymmetries, alone or in combination with low doses of specific D1 or D2 agonists, was investigated. BW 373U86 and SNC 80 failed to induce motor asymmetries by themselves, but elicited contralateral turning after pretreatment with a dose of SKF 38393, a D1 agonist, or quinpirole, a D2 agonist, which per se did not induce contralateral turning. BW 373U86 also potentiated contralateral turning induced by threshold doses of quinpirole. Facilitation of D1-dependent contralateral turning was associated with a potentiation of c-fos expression, as estimated by Fos-like immunoreactivity, in the dorsal caudate-putamen, particularly in its lateral aspect. Potentiation of D2-dependent contralateral turning was associated with a reduction of c-fos expression in the medial caudate-putamen. It is concluded that stimulation of delta-opioid receptors facilitates the expression of D1 and D2 responses arising from the denervated striatum.
在单侧6-羟基多巴胺损伤的大鼠中,研究了两种非肽类δ-阿片受体激动剂BW 373U86和SNC 80单独或与低剂量特定D1或D2激动剂联合诱导运动不对称的能力。BW 373U86和SNC 80自身未能诱导运动不对称,但在用D1激动剂SKF 38393或D2激动剂喹吡罗预处理后引发对侧旋转,而SKF 38393和喹吡罗本身不会诱导对侧旋转。BW 373U86还增强了阈剂量喹吡罗诱导的对侧旋转。通过Fos样免疫反应性估计,促进D1依赖性对侧旋转与背侧尾状核-壳核,特别是其外侧的c-fos表达增强有关。增强D2依赖性对侧旋转与内侧尾状核-壳核中c-fos表达减少有关。结论是,刺激δ-阿片受体促进了去神经纹状体产生的D1和D2反应的表达。