Abrahamsen J, Nedergaard O A
Department of Pharmacology, School of Medicine, Odense University, Denmark.
Naunyn Schmiedebergs Arch Pharmacol. 1991 Feb;343(2):161-5. doi: 10.1007/BF00168604.
The aim of the present investigation was to examine whether or not presynaptic facilitatory beta-adrenoceptors are detectable on the postganglionic nerves in the rabbit isolated ear artery. Strips of rabbit central ear artery were incubated with 3H-noradrenaline (10(-7) mol/l; 30 min or 10(-6) mol/l; 60 min). Subsequently, they were washed repeatedly with physiological salt solution. The strips were subjected to electrical-field stimulation (S1-S8) and the resultant 3H-overflow was determined. When the ear artery was stimulated with 150 pulses (0.5 ms; 3 Hz; 225 mA), isoprenaline (10(-9)-10(-6) mol/l) either alone or in the presence of either rauwolscine (10(-6) mol/l) or phentolamine (10(-6) mol/l) did not alter the stimulation-evoked 3H-overflow. This was also the case in the presence of rauwolscine (10(-6) mol/l) plus either the selective phosphodiesterase inhibitor ICI 63 197 (3 x 10(-5) mol/l) or forskolin (10(-6) mol/l). When the ear artery was stimulated with 300 pulses (1 ms; 5 Hz; 225 mA), isoprenaline had no effect on the stimulation-evoked 3H-overflow. This was also the case when phentolamine (10(-6) mol/l) was present. Propranolol (10(-7)-10(-5) mol/l) did not alter the stimulation-evoked 3H-overflow. In some experiments, the stimulation current was reduced to 175 mA in order to obtain similar reference release (S3) values despite the presence of rauwolscine (150 pulses; 0.5 ms; 3 Hz). Even then, isoprenaline (10(-9)-10(-6) mol/l) did not change stimulation-evoked 3H-overflow. The results suggest that postganglionic sympathetic nerves in rabbit central ear artery do not possess presynaptic facilitatory beta-adrenoceptors.
本研究的目的是检测家兔离体耳动脉的节后神经上是否存在突触前易化性β-肾上腺素能受体。将家兔中耳动脉条与3H-去甲肾上腺素(10(-7)mol/L;30分钟或10(-6)mol/L;60分钟)一起孵育。随后,用生理盐溶液反复冲洗。对动脉条施加电场刺激(S1-S8),并测定由此产生的3H溢出量。当耳动脉用150个脉冲(0.5毫秒;3赫兹;225毫安)刺激时,单独使用异丙肾上腺素(10(-9)-10(-6)mol/L)或在存在萝芙木碱(10(-6)mol/L)或酚妥拉明(10(-6)mol/L)的情况下,均未改变刺激诱发的3H溢出量。在存在萝芙木碱(10(-6)mol/L)加上选择性磷酸二酯酶抑制剂ICI 63 197(3×10(-5)mol/L)或福斯可林(10(-6)mol/L)的情况下也是如此。当耳动脉用300个脉冲(1毫秒;5赫兹;225毫安)刺激时,异丙肾上腺素对刺激诱发的3H溢出量没有影响。在存在酚妥拉明(10(-6)mol/L)时也是如此。普萘洛尔(10(-7)-10(-5)mol/L)没有改变刺激诱发的3H溢出量。在一些实验中尽管存在萝芙木碱(150个脉冲;0.5毫秒;3赫兹),为了获得相似的参考释放(S3)值,将刺激电流降至175毫安。即便如此,异丙肾上腺素(10(-9)-10(-6)mol/L)也没有改变刺激诱发的3H溢出量。结果表明,家兔中耳动脉的节后交感神经不具有突触前易化性β-肾上腺素能受体。