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2702

(J South Med Univ)

2010;30(12)

NR2B
/ 510080
(CCI) NR2B
SD 200~280 g 40 4 CCI
CCI CCI CCI 713 d Western
blot NR2B CCI CCI CCI
P<0.05 CCI P<0.05 CCI NR2B P<0.05
NR2B P>0.05
CCI NR2B
NMDA
R616.1

1673-4254(2010)12-2702-03

Effect of electroacupuncture on pain threshold and spinal NR2B subunit expression in a rat
model of neuropathic pain
ZHOU Guo-bin, MA Wei-tao, YU Wei, GUO Ai-lin, JI Jin-quan
Department of Anesthesiology, Guangdong General Hospital, Guangzhou 510080, China
Abstract: Objective To observe the effect of electroacupuncture (EA) on pain threshold and spinal NR2B subunit expression
in a rat model of neuropathic pain due to chronic compression injury (CCI) of the sciatic nerve and explore the analgesic
mechanism of EA. Methods Male SD rats weighing 200-280 g were randomly divided into 4 groups (n=10), namely the
sham-operated group, CCI group, EA+CCI group, and sham EA+CCI group. All the rats underwent tests of the mechanical
withdrawal threshold and thermal threshold. On day 13 after the surgery, all the rats were decapitated to collect the L4-6
segments of the spinal cord to examine NR2B expression using Western blotting. Results The postoperative mechanical
withdrawal threshold and thermal threshold were significantly lowered in CCI, EA+CCI and sham EA+CCI groups as
compared to those before the surgery (P<0.05). EA obviously alleviated the hypersensitivity in the rats with CCI and inhibited
spinal NR2B expressions (P<0.05). No significant differences were found in the mechanical withdrawal threshold, thermal
threshold or spinal NR2B subunit expression between CCI group and sham EA+CCI group (P>0.05). Conclusion EA may
alleviate neuropathic hypersensitivity partially by inhibiting NR2B expression in the spinal cord of rats with neuropathic pain
resulting from CCI of the sciatic nerve.
Key words: neuropathic pain; electroacupuncture; spinal cord; NMDA receptor

1-2N- -D

(NMDA)
3-5
NR2B

6-8
NR2B

2010-06-03
93048
(1966-)E-mail: tiramisu.yy@163.
com

1
1.1
SD 200~280 g
4
(CCI)(n=10)
CCI CCI n=10
CCI (n=10) 7
CCI (n=10) 7

1.2 CCI
1% 40 mg/kg

4-0 4

12

2703

, . NR2B

1.3
7 d

CCI
P<0.05 13 dCCI


(2~100 Hz) 0.512 mA

7 d
7 d

10 min 1 30 min 1 4

7 d

1.4 CCI

P>0.05, 12

713
von Frey
8:00 am~5:00 pm
20~24


PWL 5 min 1 , 3


20 s
Von Frey
34

90
10 5

1 g, n=10

7 d

13 d

15.00.9

14.10.8

14.70.7

CCI

14.80.7

3.90.8*

5.30.9*

CCI

15.30.7

3.51.0*

10.21.1*#

CCI

14.70.5

3.31.1*

7.50.9*

*P<0.05 vs sham group #P<0.05 vs CCI group

2 s, n=10

7 d

13 d

16.12.3

15.12.8

16.73.7

CCI

15.82.1

5.91.8*

6.31.9*

CCI

16.03.0

6.52.0*

13.23.1#

14.92.8

5.32.1*

9.02.9*

CCI

*P<0.05 vs sham group #P<0.05 vs CCI group

13 d CCI

1.5 NR2B
13 d

CCI CCI NR2B


P<0.05 CCI CCI

L4-5
-80 Western blot

NR2B P<0.05
CCI NR2B

NR2B

50 g 7.5%SDS-PAGE
5% 1 h

4 NR2B (1500) TBS

(15000) 2 h ECL
NR2B -actin
NR2B
1.6

CCI NR2B
CCI
P>0.05, 3
3 13 d NR2B n=10

NR2B

25.373.89

CCI

78.656.27*

CCI

39.215.99*#

CCI

61.856.11*

*P<0.05 vs P<0.05 vs CCI


#

t
SPSS13.0 P<0.05

P>0.05 CCI

CCI CCI 7 d

2704

(J South Med Univ)

N- -D
(NMDA) NR1

30

1 Sandkuhler J. Understanding LTP in pain pathwaysJ. Mol Pain,


2007, 3: 9.

NR2A-D NR3 NR2B


I

2 Woolf CJ. Central sensitization: uncovering the relation between

10
11-12 NMDA

4 Chizh BA, Headley PM. NMDA antagonists and neuropathic pain-

NR2B NMDA
NR2B NMDA

NR2B
Bennett9
(CCI) 3 d

7 d 13 d

13 d CCI
NR2B

NR2B NR2B


13-15

NMDA


CCI 4 13 d
16-17

7 d

CCI NR2B

CCI NR2B
P<0.05 NMDA
NR2B
NR2B

pain and plasticityJ. Anesthesiology, 2007, 106: 864-7.

3 Bleakman D, Alt A, Nisenbaum ES. Glutamate receptors and pain


J. Semin Cell Dev Biol, 2006, 17(5): 592-604.

multiple drug targets and multiple usesJ. Curr Pharm Des, 2005,
11: 2977-94.

5 Salter MW. Cellular signaling pathways of spinal pain neuroplasticity as targets for analgesic developmentJ. Curr Top Med Chem,
2005, 5: 557-67.
6

Boyce S, Wyatt A, Webb JK, et a1.

Selective NMDA NR2B

antagonists induce antinociception without motor dysfunction


correlation with restricted 1ocalisation of NR2B subunit in dorsa1
hornJ. Neuropharmacology, 1999, 38 : 611-23

7 Laurie DJ, Bartke I, Schoepfer R, et al. Regional developmental and

interspecies expression of the four NMDAR2 subunits examined


using monoclonal antibodiesJ. Brain Res, 1997, 51: 23-32.

8 Nagy GG, Watanabe M, Fukaya M, et al. Synaptic distribution of the


NR1,

NR2A and NR2B subunits of the N-methyl-D-aspartate

receptor in the rat lumbar spinal cord revealed with an antigenunmasking techniqueJ. Eur J Neurosci, 2004, 20: 3301-12.
9 Bennett GJ, Xie YK.

A peripheral mononeuropathy in rat that

produces disorders of pain sensation like those seen in man J.


Pain, 1988, 33: 87-107.

10 Boyce S, Wyatt A, Webb JK, et a1. Selective NMDA NR2B


antagonists induce antinociception without motor dysfunction:

correlation with restricted 1ocalisation of NR2B subunit in dorsa1


hornJ. Neuropharmacology1999, 38 : 611-23.
11 Loftis JM, Janowsky A. The N-methyl-D-aspartate receptor subunit
NR2B: localization, functional properties, regulation, and clinical
implicationsJ. Pharmacol Ther, 2003, 97(1): 55-85.
12 . N- -D- NMDAJ.
, 2005, 1(2): 111-4.

13 , , , .
J. , 2000, 20(12): 741-2.

14 , , . P
J. , 2006, 12(1): 11-3.

15 , , , .

EAAs J. , 2008, 27(1):

45-8.

CCI

16 . 31 J. ,

NR2B
NR2B

17 . 26 J. , 2006, 25

2007, 23(5): 27-8.

(11): 25.

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