Liquiritin alleviates spinal cord injury through suppression of inflammation, oxidative stress, and cell apoptosis in a rat model

被引:2
作者
Luo, Yongsheng [1 ]
Chen, Shihai [2 ]
Li, Ting [3 ]
Guan, Yonglin [1 ]
Liu, Yongming [1 ]
Ma, Binxiang [1 ]
机构
[1] Gansu Prov Hosp Tradit Chinese Med, Dept Spine Orthoped, Lanzhou 730050, Gansu, Peoples R China
[2] Gansu Prov Hosp Tradit Chinese Med, Dept Pediat Orthopaed, Lanzhou 730050, Gansu, Peoples R China
[3] Lanzhou Univ, Hosp 1, Donggang Hosp, Dept Hematol, Lanzhou 730000, Gansu, Peoples R China
关键词
Liquiritin; Spinal cord injury (SCI); Inflammation; Oxidative stress; Apoptosis; FUNCTIONAL RECOVERY; ANTIOXIDANT; EXPRESSION; INCREASE;
D O I
10.4314/tjpr.v18i8.17
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Purpose: Liquiritin is an extract from Glycyrrhiza Radix, one of the oldest traditional Chinese herbal medicines, which is commonly used to treat various injuries and swellings. This study is aimed to determine whether liquiritin can protect spinal cord injuries (SCIs) from secondary injuries. Methods: A rat SCI model was established. After liquiritin treatment, the neural-function of Rats was determined by Basso, Beattie and Bresnahan (BBB) scores, paw withdrawal threshold (PWT), and thermal withdrawal latency (PWL). The effects of anti-inflammation, anti-oxidation, and anti-apoptosis of liquiritin were also examined in the rats with SCI. Moreover, the activities of several signaling elements, such as, inflammation-associated nuclear factor kappa-light-chain-enhancer of activated B cells (NF-kappa B), toll-like receptor 4 (TLR4), proliferative-related p38 mitogen-activated protein kinases (MAPK) and myeloid differentiation primary response 88 (MyD88) which was involved in the TLR4 signaling, were used for further investigation of the underlying molecular mechanisms. Results: Liquiritin improved locomotor function recovery, alleviated allodynia and hyperalgesia, and decreased water content of spinal cord in SCI rats. Also, liquiritin reduced SCI-induced inflammatory responses by decreasing the levels of tumor necrosis factor alpha (TNF-alpha), interleukin 1 beta (IL-1 beta), and IL-6. Liquiritin inhibited SCI-induced oxidative stress by decreasing malondialdehyde (MDA) level and increasing the levels of uperoxide dismutase (SOD) (p < 0.05), glutathione (GSH) (p < 0.01), and GSH-PX (p < 0.001). In addition, liquiritin alleviated spinal cord injury (SCI) -induced apoptosis of neural cells by decreasing the expression of cleaved caspase-9, -3 and cleaved poly ADP-ribose polymerase (PARP). Finally, liquiritin decreased spinal cord injury (SCI) -induced up-regulation of TLR4/MyD88/NF(Sic)-kappa B and p38 MAPK signaling cascades. Conclusion: Liquiritin exerts protective role in SCI by reducing excessive inflammation, suppressing oxidative stress, and inhibiting neural cell apoptosis in a rat model of SCI. Thus, the agent can potentially be used for the management of SCI
引用
收藏
页码:1683 / 1689
页数:7
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