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1 n a rat model of neuropathic pain induced by spinal nerve ligation.
2 development of mechanical allodynia after L5 spinal nerve ligation.
3 n the absence of injury and 2 weeks after L5 spinal nerve ligation.
4 tions such as peripheral inflammation and L5 spinal nerve ligation.
5 ute to mechanical hypersensitivity following spinal nerve ligation.
6 on in the sciatic nerve of the rat following spinal nerve ligation.
7 Sprague-Dawley rats underwent left L5 and L6 spinal nerve ligation.
8 ared nerve injury, chronic constriction, and spinal nerve ligation.
9 discharges of injured sensory neurons after spinal nerve ligation.
10 lmost all ectopic discharges originate after spinal nerve ligation.
11 gesia and allodynia in the hind paw after L5 spinal nerve ligation.
12 cally characterized neurons in the RVM after spinal nerve ligation, a model of neuropathic pain that
14 G was extensive as early as 2 days after the spinal nerve ligation, and the sprouted fibers were almo
15 dorsal horn was dramatically increased after spinal nerve ligation, and this was abolished by saporin
17 vity was lost in the hind paw ipsilateral to spinal nerve ligation, but maintained in the contralater
20 a in a variety of rat pain models including: spinal nerve ligation (ED(50) = 47 mg/kg, i.p.), sciatic
24 in-43 (GAP-43) in the L5 DRG 1 week after L5 spinal nerve ligation, indicated sprouting of sympatheti
30 ing, and attenuated tactile allodynia in the spinal nerve ligation model of neuropathic pain (ED(50)=
31 reverse thermal hyperalgesia in vivo in the spinal nerve ligation model of neuropathic pain with exc
38 logical studies were performed 14-18 d after spinal nerve ligation or sham surgery, and the effects o
43 utely isolated from normal rats (no previous spinal nerve ligation) responded to either mATP or ATP.
44 e (vector QHGAD67) 7 days after selective L5 spinal nerve ligation reversed mechanical allodynia and
45 ivo studies in a rat neuropathic pain model (spinal nerve ligation) showed dose-dependent antiallodyn
49 rats and in rats that had received L5 and L6 spinal nerve ligation (SNL) immediately before injection
54 In this study, immunoblotting showed that spinal nerve ligation (SNL) induced a delayed and sustai
59 PPQ) model of acute visceral pain, and a rat spinal nerve ligation (SNL) model of neuropathic pain.
61 dependent flush as well as the hot plate and spinal nerve ligation (SNL) models of acute and neuropat
62 20 was also studied in the rat hot plate and spinal nerve ligation (SNL) models of acute and neuropat
63 ur present study, we examined the effects of spinal nerve ligation (SNL) on the number of neurons in
64 erve injury caused by the fourth lumbar (L4) spinal nerve ligation (SNL) or chronic constriction inju
66 lated from neuropathic rats induced by L5/L6 spinal nerve ligation (SNL) via electrophysiological and
67 ury models: sciatic nerve transection (SNT), spinal nerve ligation (SNL), and chronic constriction in
68 mized neurons from rats made hyperalgesic by spinal nerve ligation (SNL), basal K(ATP) channel activi
70 C-fiber-evoked potentials in rats receiving spinal nerve ligation (SNL), but not in uninjured rats.
71 verses neuropathic pain behavior after L5/L6 spinal nerve ligation (SNL), implicating a critical func
72 olving Sprague Dawley rats, we reported that spinal nerve ligation (SNL), in addition to causing allo
73 o rat model of neuropathy, unilateral lumbar spinal nerve ligation (SNL), to characterize the distrib
74 FA)-induced chronic inflammatory pain and L5 spinal nerve ligation (SNL)-induced neuropathic pain in
75 ed protein response (UPR) activation in a L5 spinal nerve ligation (SNL)-induced rat neuropathic pain
86 ion in naive, sham-operated and neuropathic (spinal nerve ligation, SNL) rats using in vivo electroph
87 ; AXO, partial sciatic nerve ligation; PSNL, spinal nerve ligation; SNL or chronic constriction injur
89 nglionic neurons was greatly increased after spinal nerve ligation, suggesting the increased number o