Institute of Physiology and Pathophysiology Friedrich-Alexander-University of Erlangen-Nürnberg Erlangen Germany.
Geistlich Pharma AG Wolhusen Switzerland.
Pharmacol Res Perspect. 2016 Feb 1;4(1):e00204. doi: 10.1002/prp2.204. eCollection 2016 Feb.
Taurolidine has long been in clinical use as an antimicrobial irrigation that does not impede wound healing. It can even be administered intravenously (30 g/day) to treat sepsis or to exert newly recognized antineoplastic actions. Only one irritant effect is reported, that is, to temporarily induce burning pain of unknown origin when applied to body cavities or peripheral veins. The structure of the molecule suggested the chemoreceptor channel TRPA1 as a potential target, which was verified measuring stimulated CGRP release from sensory nerves of the isolated mouse trachea and calcium influx in hTRPA1-transfected HEK293 cells. With both methods, the concentration-response relationship of taurolidine exceeded the threshold value below 500 μmol/L and 100 μmol/L, respectively, and reached saturation at 1 mmol/L. The clinical 2% taurolidine solution did not evoke greater or longer lasting responses. The reversible tracheal response was abolished in TRPA1(-/-) but retained in TRPV1(-/-) mice. Consistently, hTRPV1-HEK showed no calcium influx as a response, likewise native HEK293 cells and hTRPA1-HEK deprived of extracellular calcium did not respond to taurolidine 1 mmol/L. The metabolite taurultam and its oxathiazine derivative, expected to cause less burning pain, showed weak tracheal irritancy only at 10 mmol/L, acting also through hTRPA1 but not hTRPV1. In conclusion, taurolidine, its metabolite, and a novel derivative showed no unspecific cellular effects but selectively, concentration-dependently and reversibly activated the irritant receptor TRPA1 in CGRP-expressing, thus nociceptive, neurons. The clinical solution of 2% taurolidine (~70 mmol/L) can, thus, rightly be expected to cause transient burning pain and neurogenic inflammation.
牛磺酸具有长期的临床应用抗菌冲洗,不阻碍伤口愈合。它甚至可以静脉内给药(30g/天)治疗败血症或发挥新发现的抗肿瘤作用。只有一种刺激性作用,即当应用于体腔或外周静脉时,暂时引起未知来源的烧灼感。分子结构提示化学感受器通道 TRPA1 作为一个潜在的靶点,这一点通过测量从分离的小鼠气管的感觉神经刺激 CGRP 释放和 hTRPA1 转染的 HEK293 细胞钙内流来验证。用这两种方法,牛磺酸的浓度-反应关系分别在低于 500μmol/L 和 100μmol/L 的阈值以下超过阈值,并在 1mmol/L 时达到饱和。临床 2%牛磺酸溶液没有引起更大或更持久的反应。TRPA1(-/-) 小鼠中可逆转的气管反应被消除,但 TRPV1(-/-) 小鼠中保留。一致地,hTRPV1-HEK 没有作为响应的钙内流,同样,没有细胞外钙的天然 HEK293 细胞和 hTRPA1-HEK 也不响应 1mmol/L 的牛磺酸。代谢物牛磺脲和其氧杂噻嗪衍生物,预计引起较少的烧灼感,仅在 10mmol/L 时表现出微弱的气管刺激性,也通过 hTRPA1 但不通过 hTRPV1 起作用。总之,牛磺酸、其代谢物和一种新的衍生物没有显示出非特异性的细胞作用,但选择性地、浓度依赖性地和可逆地激活了 CGRP 表达的、因此是伤害性的神经元中的刺激性受体 TRPA1。临床应用的 2%牛磺酸(~70mmol/L)因此可以合理地预期引起短暂的烧灼感和神经源性炎症。