Fujiwara S, Itoh T, Suzuki H
Br J Pharmacol. 1982 Oct;77(2):197-208. doi: 10.1111/j.1476-5381.1982.tb09286.x.
1 Drug actions on electrical and mechanical properties of smooth muscle cells and neuromuscular transmission in the canine cerebral arteries were investigated by use of microelectrode and isometric tension recording methods. 2 In the basilar and middle cerebral arteries, the resting membrane potentials were--49.4 mV and -51.7 mV, respectively, the length constants 0.57 mm and 0.45 mm, respectively and the time constants 142 ms and 118 ms, respectively. 3 Outward current pulses did not evoke the spike in either artery but did evoke the spike under conditions of pretreatment with 10 mM tetraethylammonium (TEA). 4 The maximum slope of depolarization produced by a ten fold increase in [K]o plotted on a log scale was 40.1 mV in the basilar artery and 42.2 mV in the middle cerebral artery. 2-Nicotinamidoethyl nitrate, the K-permeability accelerator, had no effect on the membrane potential. 5 K-free or ouabain [10(-5)M] treatment slightly depolarized the membrane. Re-addition of K [5.9 mM] hyperpolarized the membrane by several mV. Thus, the contribution of an active Na-K pump in the membrane potential seems to be small. 6 In both arteries, acetylcholine, adenosine, noradrenaline and isoprenaline in concentrations up to 10(-5)M did not modify the membrane potential and resistance, while 5-hydroxytryptamine (over 10(-8)M) and ATP (over 10(-5)M) depolarized the membrane, decreased the membrane resistance and produced a dose-dependent contraction. Adenosine suppressed the contraction evoked by excess [K]o (39.8 mM). 7 Perivascular nerve stimulation produced excitatory junction potentials (e.j.ps). Often e.j.ps were followed by a hyperpolarization. Repetitive stimulation produced facilitation after several stimuli and depression followed. In some cells, this depression appeared without facilitation. 8 The e.j.ps ceased with pretreatment with guanethidine (10(-6)M) or tetrodotoxin (3 X 10(-7)M), while phentolamine (10(-7)M) and yohimbine (10(-7)M) enhanced the amplitude of e.j.ps. ATP (10(-5)M) and noradrenaline (10(-6)M) suppressed and prazosin had little effect on the e.j.ps. Atropine (10(-6)M) also had no effect on the e.j.ps. 9 Specific features of the cerebral artery and systemic vascular beds were compared, and the features of adrenoceptors on the smooth muscle membrane were compared with findings in other vascular beds.
采用微电极和等长张力记录方法,研究了药物对犬脑动脉平滑肌细胞电和机械特性以及神经肌肉传递的作用。
在基底动脉和大脑中动脉中,静息膜电位分别为-49.4mV和-51.7mV,长度常数分别为0.57mm和0.45mm,时间常数分别为142ms和118ms。
外向电流脉冲在两条动脉中均未引发动作电位,但在10mM四乙铵(TEA)预处理条件下可引发动作电位。
以对数标度绘制的[K]o增加10倍所产生的去极化最大斜率,在基底动脉中为40.1mV,在大脑中动脉中为42.2mV。钾通透性促进剂2-烟酰胺基乙基硝酸盐对膜电位无影响。
无钾或哇巴因[10(-5)M]处理使膜轻度去极化。重新加入钾[5.9mM]使膜超极化数毫伏。因此,膜电位中主动钠钾泵的作用似乎较小。
在两条动脉中(浓度高达10(-5)M时),乙酰胆碱、腺苷、去甲肾上腺素和异丙肾上腺素均未改变膜电位和电阻,而5-羟色胺(超过10(-8)M)和ATP(超过10(-5)M)使膜去极化、降低膜电阻并产生剂量依赖性收缩。腺苷抑制过量[K]o(39.8mM)引发的收缩。
血管周围神经刺激产生兴奋性接头电位(e.j.ps)。e.j.ps常继以超极化。重复刺激在数次刺激后产生易化,随后出现抑制。在一些细胞中,这种抑制在无易化的情况下出现。
用胍乙啶(10(-6)M)或河豚毒素(3×10(-7)M)预处理后,e.j.ps消失,而酚妥拉明(10(-7)M)和育亨宾(10(-7)M)增强e.j.ps的幅度。ATP(10(-5)M)和去甲肾上腺素(10(-6)M)抑制e.j.ps,哌唑嗪对e.j.ps影响不大。阿托品(10(-6)M)对e.j.ps也无影响。
比较了脑动脉和全身血管床的特异性特征,并将平滑肌膜上肾上腺素能受体的特征与其他血管床的研究结果进行了比较。