Virginia Commonwealth University, School of Medicine, Department of Pharmacology and Toxicology, Richmond, VA, 23298, USA.
Uludag University, Experimental Animals Breeding and Research Center, Faculty of Medicine, Bursa, Turkey.
Neuropharmacology. 2017 May 1;117:305-315. doi: 10.1016/j.neuropharm.2017.02.020. Epub 2017 Feb 22.
Paclitaxel, one of the most commonly used cancer chemotherapeutic drugs, effectively extends the progression-free survival of breast, lung, and ovarian cancer patients. However, paclitaxel and other chemotherapy drugs elicit peripheral nerve fiber dysfunction or degeneration that leads to peripheral neuropathy in a large proportion of cancer patients. Patients receiving chemotherapy also often experience changes in mood, including anxiety and depression. These somatic and affective disorders represent major dose-limiting side effects of chemotherapy. Consequently, the present study was designed to develop a preclinical model of paclitaxel-induced negative affective symptoms in order to identify treatment strategies and their underlying mechanisms of action. Intraperitoneal injections of paclitaxel (8 mg/kg) resulted in the development and maintenance of mechanical and cold allodynia. Carboplatin, another cancer chemotherapeutic drug that is often used in combination with paclitaxel, sensitized mice to the nociceptive effects of paclitaxel. Paclitaxel also induced anxiety-like behavior, as assessed in the novelty suppressed feeding and light/dark box tests. In addition, paclitaxel-treated mice displayed depression-like behavior during the forced swim test and an anhedonia-like state in the sucrose preference test. In summary, paclitaxel produced altered behaviors in assays modeling affective states in C57BL/6J male mice, while increases in nociceptive responses were longer in duration. The characterization of this preclinical model of chemotherapy-induced allodynia and affective symptoms, possibly related to neuropathic pain, provides the basis for determining the mechanism(s) underlying severe side effects elicited by paclitaxel, as well as for predicting the efficacy of potential therapeutic interventions.
紫杉醇是最常用的癌症化疗药物之一,它能有效延长乳腺癌、肺癌和卵巢癌患者的无进展生存期。然而,紫杉醇和其他化疗药物会引起周围神经纤维功能障碍或变性,导致大部分癌症患者出现周围神经病变。接受化疗的患者还经常出现情绪变化,包括焦虑和抑郁。这些躯体和情感障碍是化疗的主要剂量限制副作用。因此,本研究旨在建立紫杉醇诱导的负面情感症状的临床前模型,以确定治疗策略及其潜在的作用机制。紫杉醇(8mg/kg)腹腔注射可导致机械性和冷感觉异常痛觉过敏的发展和维持。卡铂是另一种常用于与紫杉醇联合使用的癌症化疗药物,它使小鼠对紫杉醇的痛觉作用敏感。紫杉醇还引起了新奇性抑制进食和明暗箱测试中的焦虑样行为。此外,在强迫游泳试验中,紫杉醇处理的小鼠表现出抑郁样行为,在蔗糖偏好试验中表现出快感缺失样状态。总之,紫杉醇在 C57BL/6J 雄性小鼠的情感状态测定中引起了行为改变,而痛觉反应的增加持续时间更长。这种化疗引起的痛觉过敏和情感症状的临床前模型的特征,可能与神经病理性疼痛有关,为确定紫杉醇引起的严重副作用的机制以及预测潜在治疗干预措施的疗效提供了基础。