WANG Wen-qian, TONG Dong, HUANG Wan-yi, et al. Effect of Cinnamomi Ramulus in Resisting Ephedrine Herba Central Oxidant Damages and NLRP3 Inflammasome Up-regulation[J]. Chinese journal of experimental traditional medical formulae, 2017, 23(17): 133-137.
DOI:
WANG Wen-qian, TONG Dong, HUANG Wan-yi, et al. Effect of Cinnamomi Ramulus in Resisting Ephedrine Herba Central Oxidant Damages and NLRP3 Inflammasome Up-regulation[J]. Chinese journal of experimental traditional medical formulae, 2017, 23(17): 133-137. DOI: 10.13422/j.cnki.syfjx.2017170133.
Effect of Cinnamomi Ramulus in Resisting Ephedrine Herba Central Oxidant Damages and NLRP3 Inflammasome Up-regulation
目的:研究桂枝对麻黄中枢神经系统损伤的保护作用,并初步探讨其保护作用机制。方法:KM小鼠按体重随机分为生理盐水组,麻黄组(10 g ·kg-1),麻黄-桂枝3:2组(10 g ·kg-1+6.67 g ·kg-1),麻黄-桂枝3:1组(10 g ·kg-1+3.33 g ·kg-1),桂枝组(6.67 g ·kg-1),灌胃给药14 d,酶联免疫吸附(ELISA)法检测各组小鼠脑组织中超氧化物歧化酶(SOD)
Objective: To investigate the underlying mechanism of Cinnamomi Ramulus (CR)' s protective effect on the central nervous system damages in mice induced by Ephedrine Herba (EH). Method: According to weight
KM mice were randomly assigned into saline group
EH group
EH-CR 3: 2 group
EH-CR 3: 1 group and CR group. After intragastric administration for 14 days
superoxide dismutase (SOD)
malondialdehyde (MDA)
nitric oxide (NO)
and nitric oxide synthase (NOS) levels in brain tissues were detected with ELISA
and NLRP3 inflammasome was detected by Western blot. Result: As compared with the normal saline group
SOD activity was reduced in EH group
while the levels of MDA
NO
TNOS and iNOS were increased (P<0.01); the expression levels of Nod-like receptor protein 3(NLRP3)
apoptosis-associated speck-like protein(ASC) and cysteine aspartic acid protease-1(Caspase-1) were up-regulated (P<0.01); but CR group showed no significant difference. As compared with EH group
CR combined with EH could significantly increase SOD activity in brain tissue (P<0.05
P<0.01)
reduce the MDA
NO
TNOS
iNOS production(P<0.05
P<0.01)
and down-regulate the NLRP3
ASC and Caspase-1 protein expressions (P<0.05
P<0.01). Conclusion: CR has protective effect on the central nervous system damages induced by EH
and its mechanism may be associated with increasing antioxidant ability
reducing oxidant damage and attenuating NLRP3 inflammasome expression.
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