Shafton A D, Bogeski G, Kitchener P D, Lewis V A, Sanger G J, Furness J B
Department of Anatomy and Cell Biology and Centre for Neuroscience, University of Melbourne, Parkville, Victoria, Australia.
Neurogastroenterol Motil. 2004 Apr;16(2):223-31. doi: 10.1111/j.1365-2982.2004.00501.x.
We investigated the effects of the selective NK(3) tachykinin receptor antagonist, SB-235375, on noxious signalling from gut and skin and on intestinal motility in anaesthetized rats. We also measured penetrance into brain and spinal cord. Nociceptive responses in reaction to colorectal distension and skin pinch were assessed by recording the electromyogram (EMG) from the external oblique muscle (a visceromotor response). Motility was measured by recording intraluminal pressure waves during changes in baseline pressure in the jejunum. Colorectal compliance was assessed by measuring luminal pressure change during isovolumic distension. SB-235375 (20 mg kg(-1), by i.v. bolus) reduced the EMG response to colorectal distension by over 90%. The reduction was slow at onset, peaked at about 60 min, and lasted for over 2 h. Responses to noxious skin pinch were unchanged. Amplitudes of propulsive waves in the jejunum were slightly reduced, but their frequency of occurrence was unchanged. SB-235375 decreased colorectal compliance by 5-10%. There was undetectable penetration of i.v. SB-235375 into brain or spinal cord. We conclude that SB-235375 acts peripherally to substantially reduce nociceptive signalling from colorectum without affecting noxious signalling from skin and with little effect on intestinal motility.
我们研究了选择性NK(3)速激肽受体拮抗剂SB - 235375对麻醉大鼠肠道和皮肤伤害性信号传导以及肠道运动的影响。我们还测量了其在脑和脊髓中的渗透率。通过记录腹外斜肌的肌电图(EMG,一种内脏运动反应)来评估对结直肠扩张和皮肤捏夹的伤害性反应。通过记录空肠基线压力变化期间的腔内压力波来测量肠道运动。通过测量等容扩张期间的腔内压力变化来评估结直肠顺应性。SB - 235375(静脉推注,20 mg kg(-1))使对结直肠扩张的EMG反应降低了90%以上。这种降低起效缓慢,在约60分钟时达到峰值,并持续超过2小时。对伤害性皮肤捏夹的反应未改变。空肠推进波的幅度略有降低,但其出现频率未改变。SB - 235375使结直肠顺应性降低了5 - 10%。静脉注射的SB - 235375在脑或脊髓中未检测到渗透。我们得出结论,SB - 235375在周围发挥作用,可大幅降低来自结直肠的伤害性信号传导,而不影响来自皮肤的伤害性信号传导,且对肠道运动影响较小。