Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/29338
Title: Effects of paclitaxel on the development of neuropathy and affective behaviors in the mouse
Authors: Toma, Wisam
Kyte, S. Lauren
Alkhlaif, Yasmin
Alsharari, Shakir D.
Lichtman, Aron H.
Chen, Zhi-Jian
Del fabbro, Egidio
Bigbee, John W.
Gewirtz, David A.
Damaj, M. Imad
Uludağ Üniversitesi/Veteriner Fakültesi/Deney Hayvanları Yetiştirme ve Araştırma Merkezi.
Bağdas, Deniz
15062425700
Keywords: Neurosciences & neurology
Pharmacology & pharmacy
Induced peripheral neuropathy
Quality of life
Breast cancer
In vivo
Pain
Chemotherapy
Prevalence
Cisplatin
Model
Phass III
Issue Date: 1-May-2017
Publisher: Elsevier
Citation: Toma, W. vd. (2017). ''Effects of paclitaxel on the development of neuropathy and affective behaviors in the mouse''. Neuropharmacology, 117, 305-315.
Abstract: 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.
URI: https://doi.org/10.1016/j.neuropharm.2017.02.020
https://www.sciencedirect.com/science/article/pii/S0028390817300746
http://hdl.handle.net/11452/29338
ISSN: 0028-3908
1873-7064
Appears in Collections:Scopus
Web of Science

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