Targeting cannabinoid signaling for peritoneal dialysis-induced oxidative stress and fibrosis.

Chih-Yu Yang, Yat-Pang Chau, Ann Chen, Oscar Kuang-Sheng Lee, Der-Cherng Tarng, An-Hang Yang
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引用次数: 8

Abstract

Long-term exposure to bioincompatible peritoneal dialysis (PD) solutions frequently results in peritoneal fibrosis and ultrafiltration failure, which limits the life-long use of and leads to the cessation of PD therapy. Therefore, it is important to elucidate the pathogenesis of peritoneal fibrosis in order to design therapeutic strategies to prevent its occurrence. Peritoneal fibrosis is associated with a chronic inflammatory status as well as an elevated oxidative stress (OS) status. Beyond uremia per se, OS also results from chronic exposure to high glucose load, glucose degradation products, advanced glycation end products, and hypertonic stress. Therapy targeting the cannabinoid (CB) signaling pathway has been reported in several chronic inflammatory diseases with elevated OS. We recently reported that the intra-peritoneal administration of CB receptor ligands, including CB1 receptor antagonists and CB2 receptor agonists, ameliorated dialysis-related peritoneal fibrosis. As targeting the CB signaling pathway has been reported to be beneficial in attenuating the processes of several chronic inflammatory diseases, we reviewed the interaction among the cannabinoid system, inflammation, and OS, through which clinicians ultimately aim to prolong the peritoneal survival of PD patients.

Abstract Image

靶向大麻素信号在腹膜透析诱导的氧化应激和纤维化中的作用。
长期暴露于生物不相容的腹膜透析(PD)溶液经常导致腹膜纤维化和超滤失败,这限制了终身使用并导致PD治疗停止。因此,阐明腹膜纤维化的发病机制对于设计预防其发生的治疗策略具有重要意义。腹膜纤维化与慢性炎症状态以及氧化应激(OS)状态升高有关。除了尿毒症本身,慢性暴露于高葡萄糖负荷、葡萄糖降解产物、晚期糖基化终产物和高渗应激也会导致OS。针对大麻素(CB)信号通路的治疗已被报道用于几种伴有OS升高的慢性炎症性疾病。我们最近报道了腹膜内给药CB受体配体,包括CB1受体拮抗剂和CB2受体激动剂,改善透析相关腹膜纤维化。据报道,靶向CB信号通路有助于减轻几种慢性炎症性疾病的过程,我们回顾了大麻素系统、炎症和OS之间的相互作用,临床医生最终目的是延长PD患者的腹膜生存期。
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