Phenyl N-tert-butylnitrone, a Free Radical Scavenger, Reduces Mechanical Allodynia in Chemotherapy-induced Neuropathic Pain in Rats

被引:112
作者
Kim, Hee Kee [1 ]
Zhang, Yan Ping [1 ]
Gwak, Young Seob [1 ]
Abdi, Salahadin [1 ]
机构
[1] Univ Miami, LM Miller Sch Med, Dept Anesthesiol Perioperat Med & Pain Management, Div Pain Med, Miami, FL 33136 USA
关键词
INDUCED PERIPHERAL NEUROPATHY; DORSAL-ROOT GANGLIA; OXIDATIVE STRESS; NERVE INJURY; PROINFLAMMATORY CYTOKINES; SENSORY NEURONS; HORN NEURONS; NITRIC-OXIDE; HYPERALGESIA; TAXOL;
D O I
10.1097/ALN.0b013e3181ca31bd
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Background: Paclitaxel is a widely used chemotherapeutic drug for breast and ovarian cancer. Unfortunately, it induces neuropathic pain, which is a dose-limiting side effect. Free radicals have been implicated in many neurodegenerative diseases. The current study tests the hypothesis that a free radical scavenger plays an important role in reducing chemotherapy-induced neuropathic pain. Methods: Neuropathic pain was induced by intraperitoneal injection of paclitaxel (2 mg/kg) on four alternate days (days 0, 2, 4, and 6) in male Spraue-Dawley rats. Phenyl N-tert-butylnitrone (PBN), a free radical scavenger, was administered intraperitoneally as a single dose or multiple doses before or after injury. Mechanical allodynia was measured by using von Frey filaments. Results: The administration of paclitaxel induced mechanical allodynia, which began to manifest on days 7-10, peaked within 2 weeks, and plateaued for at least 2 months after the first paclitaxel injection. A single injection or multiple intraperitoneal injections of PBN ameliorated paclitaxel-induced pain behaviors in a dose-dependent manner. Further, multiple administrations of PBN starting on day 7 through day 15 after the first injection of paclitaxel completely prevented the development of mechanical allodynia. However, an intraperitoneal administration of PBN for 8 days starting with the first paclitaxel injection did not prevent the development of pain behavior. Conclusions: This study clearly shows that PBN alleviated mechanical allodynia induced by paclitaxel in rats. Furthermore, our data show that PBN given on days 7 through 15 after the first paclitaxel injection prevented the development of chemotherapy-induced neuropathic pain. This clearly has a clinical implication.
引用
收藏
页码:432 / 439
页数:8
相关论文
共 48 条
[1]   NMDA receptor regulation by Src kinase signalling in excitatory synaptic transmission and plasticity [J].
Ali, DW ;
Salter, MW .
CURRENT OPINION IN NEUROBIOLOGY, 2001, 11 (03) :336-342
[2]   TAXOL EFFECT ON TUBULIN POLYMERIZATION AND ASSOCIATED GUANOSINE 5'-TRIPHOSPHATE HYDROLYSIS [J].
CARLIER, MF ;
PANTALONI, D .
BIOCHEMISTRY, 1983, 22 (20) :4814-4822
[3]   QUANTITATIVE ASSESSMENT OF TACTILE ALLODYNIA IN THE RAT PAW [J].
CHAPLAN, SR ;
BACH, FW ;
POGREL, JW ;
CHUNG, JM ;
YAKSH, TL .
JOURNAL OF NEUROSCIENCE METHODS, 1994, 53 (01) :55-63
[4]   HPLC PROCEDURE FOR THE PHARMACOKINETIC STUDY OF THE SPIN-TRAPPING AGENT, ALPHA-PHENYL-N-TERT-BUTYL NITRONE (PBN) [J].
CHEN, GM ;
GRIFFIN, M ;
POYER, JL ;
MCCAY, PB .
FREE RADICAL BIOLOGY AND MEDICINE, 1990, 9 (02) :93-98
[5]  
Chung Jin Mo, 2002, Pain Pract, V2, P87, DOI 10.1046/j.1533-2500.2002.02011.x
[6]   Neuropathic pain is associated with alterations of nitric oxide synthase immunoreactivity and catalytic activity in dorsal root ganglia and spinal dorsal horn [J].
Cízková, D ;
Lukácová, N ;
Marsala, M ;
Marsala, J .
BRAIN RESEARCH BULLETIN, 2002, 58 (02) :161-171
[7]   Chronic post-ischemia pain (CPIP): a novel animal model of complex regional pain syndrome-Type I (CRPS-1; reflex sympathetic dystrophy) produced by prolonged hindpaw ischemia and reperfusion in the rat [J].
Coderre, TJ ;
Xanthos, DN ;
Francis, L ;
Bennett, GJ .
PAIN, 2004, 112 (1-2) :94-105
[8]  
Contestabile Antonio, 2001, Current Topics in Medicinal Chemistry, V1, P553, DOI 10.2174/1568026013394723
[9]   OXIDATIVE STRESS, GLUTAMATE, AND NEURODEGENERATIVE DISORDERS [J].
COYLE, JT ;
PUTTFARCKEN, P .
SCIENCE, 1993, 262 (5134) :689-695
[10]   Reversible analgesia, atonia, and loss of consciousness on bilateral intracerebral microinjection of pentobarbital [J].
Devor, M ;
Zalkind, V .
PAIN, 2001, 94 (01) :101-112