Department of Pharmacology, Yale University, New Haven, Connecticut, USA.
FASEB J. 2012 Nov;26(11):4696-709. doi: 10.1096/fj.12-214643. Epub 2012 Aug 13.
Chemotherapy-induced peripheral neuropathy (CIPN) is a debilitating side effect that occurs in many patients undergoing chemotherapy. It is often irreversible and frequently leads to early termination of treatment. In this study, we have identified two compounds, lithium and ibudilast, that when administered as a single prophylactic injection prior to paclitaxel treatment, prevent the development of CIPN in mice at the sensory-motor and cellular level. The prevention of neuropathy was not observed in paclitaxel-treated mice that were only prophylactically treated with a vehicle injection. The coadministration of lithium with paclitaxel also allows for administration of higher doses of paclitaxel (survival increases by 60%), protects against paclitaxel-induced cardiac abnormalities, and, notably, does not interfere with the antitumor effects of paclitaxel. Moreover, we have determined a mechanism by which CIPN develops and have discovered that lithium and ibudilast inhibit development of peripheral neuropathy by disrupting the interaction between paclitaxel, neuronal calcium sensor 1 (NCS-1), and the inositol 1,4,5-trisphosphate receptor (InsP3R) to prevent treatment-induced decreases in intracellular calcium signaling. This study shows that lithium and ibudilast are candidate therapeutics for the prevention of paclitaxel-induced neuropathy and could enable patients to tolerate more aggressive treatment regimens.
化疗引起的周围神经病(CIPN)是许多接受化疗的患者出现的一种使人虚弱的副作用。它通常是不可逆转的,并且经常导致治疗的早期终止。在这项研究中,我们已经确定了两种化合物,锂和伊布地尔,当它们在紫杉醇治疗前作为单一预防注射给药时,可预防小鼠在感觉运动和细胞水平上发生 CIPN。在仅用载体注射预防性治疗的紫杉醇处理的小鼠中,未观察到神经病变的预防。锂与紫杉醇的共同给药还允许给予更高剂量的紫杉醇(存活率增加 60%),防止紫杉醇引起的心脏异常,并且值得注意的是,不干扰紫杉醇的抗肿瘤作用。此外,我们已经确定了 CIPN 发展的机制,并发现锂和伊布地尔通过破坏紫杉醇、神经元钙传感器 1(NCS-1)和肌醇 1,4,5-三磷酸受体(InsP3R)之间的相互作用来抑制周围神经病的发展,以防止治疗诱导的细胞内钙信号转导降低。这项研究表明,锂和伊布地尔是预防紫杉醇引起的神经病变的候选治疗药物,并且可以使患者耐受更积极的治疗方案。