浏览全部资源
扫码关注微信
1. 南京中医药大学江苏省针灸学重点实验室
2. 江苏凯基生物技术股份有限公司
纸质出版日期:2019
移动端阅览
闫丽萍, 侯保权, 李守栋, 等. 电针对坐骨神经分支选择性损伤大鼠脊髓L-Arg/NO/cGMP通路的影响[J]. 针刺研究, 2019,44(12):893-897.
YAN Li-ping, HOU Bao-quan, LI Shou-dong, et al. Electroacupuncture relieved neuropathic pain by suppressing L-Arg/NO/cGMP pathway in the lumbar spinal cord in rats with spared nerve injury[J]. Acupuncture research, 2019, 44(12): 893-897.
闫丽萍, 侯保权, 李守栋, 等. 电针对坐骨神经分支选择性损伤大鼠脊髓L-Arg/NO/cGMP通路的影响[J]. 针刺研究, 2019,44(12):893-897. DOI: 10.13702/j.1000-0607.190096.
YAN Li-ping, HOU Bao-quan, LI Shou-dong, et al. Electroacupuncture relieved neuropathic pain by suppressing L-Arg/NO/cGMP pathway in the lumbar spinal cord in rats with spared nerve injury[J]. Acupuncture research, 2019, 44(12): 893-897. DOI: 10.13702/j.1000-0607.190096.
目的 :观察坐骨神经分支选择性损伤(SNI)大鼠脊髓相应节段左旋精氨酸(L-Arg)转运体2(CAT-2)、一氧化氮合酶(NOS)与一氧化氮(NO)和环鸟苷酸(cGMP)的变化及电针对其的影响
探讨电针干预神经病理性痛的脊髓机制。方法:SD大鼠随机分为假手术组、模型组、电针组和NOS抑制剂(LNAME)组
每组30只。采用SNI法制备神经病理性痛模型
假手术组仅分离不结扎。电针组电针大鼠损伤侧"委中""环跳"穴
频率2 Hz
波宽0. 6 ms
起始电流强度1 mA
每10 min递增1 mA
刺激时间30 min
1次/d
连续7 d;L-NAME组予L-NAME 60 mg·kg
(-1)
·d(-1)·d
(-1)
腹腔注射
连续7 d。造模前及SNI后10、16 d分别测定机械痛阈。RT-PCR法测定脊髓CAT-2 mRNA与诱导型NOS(iNOS)mRNA的表达
Western blot法测定脊髓iNOS的表达
硝酸/亚硝酸还原酶法与放射免疫分析法分别测定NO(NO_2(-1)腹腔注射
连续7 d。造模前及SNI后10、16 d分别测定机械痛阈。RT-PCR法测定脊髓CAT-2 mRNA与诱导型NOS(iNOS)mRNA的表达
Western blot法测定脊髓iNOS的表达
硝酸/亚硝酸还原酶法与放射免疫分析法分别测定NO(NO_2
-
/NO_3-/NO_3
-
)与cGMP的含量。结果:与假手术组比较
SNI后10 d其他各组机械痛阈值均降低(P
<
0. 01);与模型组比较
电针组和LNAME组SNI后16 d时机械痛阈值均升高(P
<
0. 01
P
<
0. 05)。与假手术组比较
模型组脊髓CAT-2mRNA、iNOS mRNA、iNOS蛋白表达及NO_2-)与cGMP的含量。结果:与假手术组比较
SNI后10 d其他各组机械痛阈值均降低(P
<
0. 01);与模型组比较
电针组和LNAME组SNI后16 d时机械痛阈值均升高(P
<
0. 01
P
<
0. 05)。与假手术组比较
模型组脊髓CAT-2mRNA、iNOS mRNA、iNOS蛋白表达及NO_2
-
/NO_3-/NO_3
-
与cGMP含量均升高(P
<
0. 01
P
<
0. 05);与模型组比较
电针组和L-NAME组脊髓CAT-2 mRNA、iNOS mRNA、iNOS蛋白表达及NO_2-与cGMP含量均升高(P
<
0. 01
P
<
0. 05);与模型组比较
电针组和L-NAME组脊髓CAT-2 mRNA、iNOS mRNA、iNOS蛋白表达及NO_2
-
/NO_3-/NO_3
-
与cGMP含量均下降(P
<
0. 05
P
<
0. 01)
且L-NAME组CAT-2 mRNA、iNOS mRNA、iNOS蛋白表达比电针组降低更显著(P
<
0. 05)。结论:电针缓解疼痛的作用机制之一
可能是通过有效下调神经病理性痛状态下脊髓L-Arg/NO/cGMP通路的功能而实现的。ObjectiveTo observe the effect of electroacupuncture(EA)on changes of expression of L-Arg transporter 2(CAT-2)m RNA and nitric oxide synthase(i NOS)m RNA and protein and contents of NO and c GMP of L4—L6 segments of spinal cord in rats with spared nerve injury(SNI)
so as to reveal its mechanism underlying reducing neuropathic pain.MethodsA total of 120 male SD rats were randomly divided into sham operation
model
EA and NOS inhibitor(N omega-Nitro-L-arginine methyl ester hydrochloride
L-NAME)groups
with 30 rats in each group. The neuropathic pain model was established by ligating and cutting the tibial nerve and the common peroneal nerve. EA(2 Hz
1—3 m A)was applied to"Weizhong"(BL40)and"Huantiao"(GB30)on the damaged hindlimb for 30 min
once daily from day 11 to 17 after SNI. Rats of the L-NAME group received i. p. of L-NAME(60 mg·kg-与cGMP含量均下降(P
<
0. 05
P
<
0. 01)
且L-NAME组CAT-2 mRNA、iNOS mRNA、iNOS蛋白表达比电针组降低更显著(P
<
0. 05)。结论:电针缓解疼痛的作用机制之一
可能是通过有效下调神经病理性痛状态下脊髓L-Arg/NO/cGMP通路的功能而实现的。
ObjectiveTo observe the effect of electroacupuncture(EA)on changes of expression of L-Arg transporter 2(CAT-2)m RNA and nitric oxide synthase(i NOS)m RNA and protein and contents of NO and c GMP of L4—L6 segments of spinal cord in rats with spared nerve injury(SNI)
so as to reveal its mechanism underlying reducing neuropathic pain.MethodsA total of 120 male SD rats were randomly divided into sham operation
model
EA and NOS inhibitor(N omega-Nitro-L-arginine methyl ester hydrochloride
L-NAME)groups
with 30 rats in each group. The neuropathic pain model was established by ligating and cutting the tibial nerve and the common peroneal nerve. EA(2 Hz
1—3 m A)was applied to"Weizhong"(BL40)and"Huantiao"(GB30)on the damaged hindlimb for 30 min
once daily from day 11 to 17 after SNI. Rats of the L-NAME group received i. p. of L-NAME(60 mg·kg
(-1)
·d(-1)·d
(-1)
)for 7 consecutive days.The mechanical pain threshold(PT)was determined before and 10 and 16 d after SNI
respectively. The expression levels of CAT-2 m RNA and i NOS m RNA
and i NOS protein in the L4—L6 segments of the spinal cord were detected by using reverse transcription-polymerase chain reaction(RT-PCR)and Western blot
respectively
and the contents of NO and cGMP of L4—L6 assayed using nitrate/nitrite reductase method and radioimmunoassay
respectively.Results After modeling
the PT was significantly decreased on day 10 and 16 after SNI in comparison with the sham operation group and their own baseline data of pre-operation in each group(P
<
0. 01)
and remarkably increased in the EA and L-NAME groups relevant to the model group on day 16(P
<
0. 01
P
<
0. 05). Compared with the sham operation group
the expression levels of CAT-2 mRNA and i NOS m RNA and protein
as well as the contents of NO_2(-1))for 7 consecutive days.The mechanical pain threshold(PT)was determined before and 10 and 16 d after SNI
respectively. The expression levels of CAT-2 m RNA and i NOS m RNA
and i NOS protein in the L4—L6 segments of the spinal cord were detected by using reverse transcription-polymerase chain reaction(RT-PCR)and Western blot
respectively
and the contents of NO and cGMP of L4—L6 assayed using nitrate/nitrite reductase method and radioimmunoassay
respectively.Results After modeling
the PT was significantly decreased on day 10 and 16 after SNI in comparison with the sham operation group and their own baseline data of pre-operation in each group(P
<
0. 01)
and remarkably increased in the EA and L-NAME groups relevant to the model group on day 16(P
<
0. 01
P
<
0. 05). Compared with the sham operation group
the expression levels of CAT-2 mRNA and i NOS m RNA and protein
as well as the contents of NO_2
-
/NO_3-/NO_3
-
and c GMP were significantly up-regulated in the model group(P
<
0. 05
P
<
0. 01). Following EA intervention
the levels of CAT-2 m RNA and i NOS m RNA and i NOS protein
and NO_2-and c GMP were significantly up-regulated in the model group(P
<
0. 05
P
<
0. 01). Following EA intervention
the levels of CAT-2 m RNA and i NOS m RNA and i NOS protein
and NO_2
-
/NO_3-/NO_3
-
and cGMP contents were all reversed in both EA and L-NAME groups(P
<
0. 05
P
<
0. 01). The effect of EA was significantly superior to that of L-NAME in raising the PT on day 16 after SNI(P
<
0. 05)
but obviously inferior to that of L-NAME in down-regulating the expression of CAT-2 m RNA and i NOS m RNA and protein(P
<
0. 05). No significant differences were found between the EA and L-NAME groups in down-regulating NO2-/NO3-and c GMP contents(P
>
0. 05).ConclusionEA intervention can effectively relieve neuropathic pain in SNI rats
which may be closely related to its function in suppressing L-Arg/NO/c GMP pathway in the lumbar spinal cord.
0
浏览量
300
下载量
5
CNKI被引量
关联资源
相关文章
相关作者
相关机构