Alsufyani Hadeel A, Docherty James R
Department of Physiology, King Abdulaziz University, Jeddah 21589, Saudi Arabia.
Department of Physiology, Royal College of Surgeons in Ireland (RCSI), Dublin D02 YN77, Ireland.
Korean J Physiol Pharmacol. 2021 Nov 1;25(6):525-532. doi: 10.4196/kjpp.2021.25.6.525.
We have investigated the relative roles of α-adrenoceptors and purinoceptors in contractions to low and high frequency stimulation of the mouse vas deferens, in terms of the time course of responses. In separate experiments, isometric contractile responses were obtained to 10 pulses at 1 Hz and 40 pulses at 10 Hz. Responses to 1 Hz stimulation consisted of a series of discrete peaks. The α-adrenoceptor antagonist RS100329 (10M-10M) significantly reduced the response to the first pulse, the α-adrenoceptor antagonist BMY7378 (10M-10M) significantly reduced the response to the first two pulses, and the non-selective α-adrenoceptor antagonist prazosin (10M) reduced the response to the first 4 pulses at 1 Hz. Responses to 10 Hz stimulation consisted of an early peak response and a maintained plateau response. RS100329 significantly reduced the peak response but did not significantly affect the plateau response. Prazosin, significantly reduced both the peak and plateau responses. The α-adrenoceptor antagonist RS17053 in high concentrations reduced mainly the plateau response leaving a clear early peak response. The plateau response of contraction was almost abolished by the purinoceptor antagonist suramin. These results suggest that there is a relatively minor early α-adrenoceptor and a larger early α-adrenoceptor component to stimulationevoked contractions of mouse vas deferens, but the major α-adrenoceptor component is revealed by prazosin to be α-adrenoceptor mediated. α-Adrenoceptor activation probably facilitates contractions mediated by other α-adrenoceptors and by purinoceptors. These results suggest that combined non-selective α-adrenoceptor blockade, particularly α-adrenoceptor blockade, in addition to P2X1-purinoceptor blockade is useful in reducing male fertility.
我们根据反应的时间进程,研究了α-肾上腺素能受体和嘌呤受体在小鼠输精管对低频和高频刺激收缩中的相对作用。在单独的实验中,获得了对1Hz的10个脉冲和10Hz的40个脉冲的等长收缩反应。对1Hz刺激的反应由一系列离散的峰值组成。α-肾上腺素能受体拮抗剂RS100329(10⁻⁶M - 10⁻⁸M)显著降低了对第一个脉冲的反应,α-肾上腺素能受体拮抗剂BMY7378(10⁻⁶M - 10⁻⁸M)显著降低了对前两个脉冲的反应,非选择性α-肾上腺素能受体拮抗剂哌唑嗪(10⁻⁶M)降低了对1Hz时前4个脉冲的反应。对10Hz刺激的反应由早期峰值反应和持续的平台反应组成。RS100329显著降低了峰值反应,但对平台反应没有显著影响。哌唑嗪显著降低了峰值和平台反应。高浓度的α-肾上腺素能受体拮抗剂RS17053主要降低了平台反应,留下明显的早期峰值反应。嘌呤受体拮抗剂苏拉明几乎消除了收缩的平台反应。这些结果表明,在小鼠输精管刺激诱发的收缩中,存在相对较小的早期α-肾上腺素能受体成分和较大的早期α-肾上腺素能受体成分,但哌唑嗪显示主要的α-肾上腺素能受体成分是α₁-肾上腺素能受体介导的。α-肾上腺素能受体激活可能促进由其他α-肾上腺素能受体和嘌呤受体介导的收缩。这些结果表明,联合非选择性α-肾上腺素能受体阻断,特别是α₁-肾上腺素能受体阻断,除P2X₁-嘌呤受体阻断外,对降低男性生育能力是有用的。