Craft Rebecca M, Carlisi Vincent J, Mattia Antonia, Herman Richard M, Porreca Frank
Department of Pharmacology, University of Arizona Health Sciences Center, Tucson, AZ 85724 USA.
Pain. 1993 Nov;55(2):205-215. doi: 10.1016/0304-3959(93)90149-J.
This study characterized the excitatory (nociceptive) and desensitizing (antinociceptive) properties of the natural pungent substances, capsaicin (CAP) and resiniferatoxin (RTX) instilled in the bladder (intravesical, i.ves.) via an indwelling cannula in awake, freely moving rats. The incidence of 9 behaviors was scored for 10 min following i.ves. vehicle or RTX (1.0 nmol). Abdominal licking and head-turning occurred significantly more often in RTX-treated rats compared to vehicle controls, whereas head-grooming, locomotion, rearing and biting did not differ between the two groups. Little or no vocalization, defecation or hindlimb hyperextension was observed in either RTX- or vehicle-treated rats. A second injection of either vehicle or RTX administered to RTX-treated rats 60 min later did not significantly increase abdominal licking or head-turning compared to vehicle controls; this subsequent lack of excitation was taken as a measure of desensitization. In a separate experiment, the first injection of i.ves. RTX (0.1-3.0 nmol) increased licking in a dose-dependent manner; in contrast, the first injection of i.ves. CAP (0.1-3.0 mumol) significantly increased licking only at the intermediate dose tested, 1.0 mumol. With each subsequent injection of the same drug and dose at 30-min intervals, licking increased to a lesser extent, such that it was not significantly different from control after the fourth injection. Rats treated with i.ves. CAP or RTX also did not show increased licking when administered the opposite treatment 30 min later (RTX or CAP, respectively), indicating cross-desensitization; however, i.ves. administration of a third, higher dose of RTX reinstated licking behavior in these 'desensitized' rats. Subcutaneous administration of CAP (18-180 mg/kg) or RTX (18-180 micrograms/kg) dose-dependently attenuated the excitatory response to i.ves. CAP and RTX administered 2 days later. Whereas rats treated systemically with RTX also were desensitized to the excitatory effects of RTX instilled in the eye (evaluated in the eye-wipe assay), rats treated i.ves. with RTX and vehicle-treated rats showed a normal eye-wiping response. Finally, pretreatment with i.ves. ruthenium red, a cation channel blocker, antagonized the excitatory and desensitizing effects of i.ves. RTX. This study demonstrates that repeated application of both CAP and RTX into the bladder produces behavioral effects indicative of local sensory afferent desensitization. I.ves. CAP and RTX appear to produce their excitatory and desensitizing effects via a common mechanism, which is dependent on cation channel activation.(ABSTRACT TRUNCATED AT 400 WORDS)
本研究通过在清醒、自由活动的大鼠体内留置套管向膀胱内灌注天然辛辣物质辣椒素(CAP)和树脂毒素(RTX),对其兴奋性(伤害感受性)和脱敏(抗伤害感受性)特性进行了表征。在膀胱内灌注赋形剂或RTX(1.0 nmol)后10分钟,对9种行为的发生频率进行评分。与赋形剂对照组相比,RTX处理的大鼠腹部舔舐和转头行为显著更频繁,而两组之间的头部梳理、运动、站立和咬噬行为没有差异。RTX处理组和赋形剂处理组的大鼠均很少或未观察到发声、排便或后肢过度伸展。在RTX处理的大鼠60分钟后第二次注射赋形剂或RTX,与赋形剂对照组相比,腹部舔舐或转头行为没有显著增加;随后这种缺乏兴奋的情况被视为脱敏的一种衡量指标。在另一个实验中,第一次膀胱内注射RTX(0.1 - 3.0 nmol)以剂量依赖性方式增加舔舐行为;相比之下,第一次膀胱内注射CAP(0.1 - 3.0 μmol)仅在测试的中间剂量1.0 μmol时显著增加舔舐行为。每隔30分钟以相同药物和剂量进行后续每次注射时,舔舐行为增加的程度较小,以至于在第四次注射后与对照组没有显著差异。膀胱内注射CAP或RTX处理的大鼠在30分钟后给予相反处理(分别为RTX或CAP)时也未表现出舔舐行为增加,表明存在交叉脱敏;然而,膀胱内注射第三种更高剂量的RTX可使这些“脱敏”大鼠恢复舔舐行为。皮下注射CAP(18 - 180 mg/kg)或RTX(18 - 180 μg/kg)剂量依赖性地减弱了2天后膀胱内注射CAP和RTX引起的兴奋反应。虽然全身用RTX处理的大鼠对眼内灌注RTX的兴奋作用也产生脱敏(通过擦眼试验评估),但膀胱内注射RTX的大鼠和赋形剂处理的大鼠表现出正常的擦眼反应。最后,膀胱内预先注射阳离子通道阻滞剂钌红可拮抗膀胱内注射RTX的兴奋和脱敏作用。本研究表明,向膀胱内重复应用CAP和RTX均产生指示局部感觉传入脱敏的行为效应。膀胱内注射CAP和RTX似乎通过一种共同机制产生其兴奋和脱敏作用,该机制依赖于阳离子通道激活。(摘要截选至400字)