中部战区总医院,湖北省武汉市武昌区武珞路627号,430070
hdc98@sina.com
收稿:2023-08-11,
修回:2023-10-17,
纸质出版:2023-12-17
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肖静静,何东初,张梦云等.健脾补肾方对辐射损伤模型小鼠脾脏自噬小体及PI3K/Akt/mTOR通路的影响[J].中医杂志,2023,64(24):2553-2560.
XIAO Jingjing,HE Dongchu,ZHANG Mengyun,et al.Effects of Jianpi BushenFormula (健脾补肾方) on the Autophagosomes and PI3K/Akt/mTOR Pathway in Radiation Injured Model Mice[J].Journal of Traditional Chinese Medicine,2023,64(24):2553-2560.
肖静静,何东初,张梦云等.健脾补肾方对辐射损伤模型小鼠脾脏自噬小体及PI3K/Akt/mTOR通路的影响[J].中医杂志,2023,64(24):2553-2560. DOI: 10.13288/j.11-2166/r.2023.24.012.
XIAO Jingjing,HE Dongchu,ZHANG Mengyun,et al.Effects of Jianpi BushenFormula (健脾补肾方) on the Autophagosomes and PI3K/Akt/mTOR Pathway in Radiation Injured Model Mice[J].Journal of Traditional Chinese Medicine,2023,64(24):2553-2560. DOI: 10.13288/j.11-2166/r.2023.24.012.
目的
2
探讨健脾补肾方对辐射所致免疫功能损伤的影响和可能作用机制。
方法
2
50只昆明种小鼠随机分为正常组、模型组、胸腺肽组和健脾补肾方大、小剂量组,每组10只。除正常组外其余各组小鼠采用6.0 Gy X线一次性全身照射建立辐射损伤小鼠模型。造模成功后健脾补肾方小、大剂量组小鼠分别给予13 g/(kg·d)、26 g/(kg·d)健脾补肾方灌胃,胸腺肽组小鼠给予胸腺肽肠溶片11.7 mg/(kg·d)灌胃,正常组、模型组小鼠用0.9%氯化钠溶液0.1 ml/(10 g·d)灌胃。各组均每日灌胃1次,连续7天。最后一次灌胃后,小鼠称重,处死后分离小鼠脾脏,称重并计算脾脏指数;ELISA法检测脾脏组织干扰素γ(IFN-γ)、白细胞介素2(IL-2)含量;透射电镜观察脾脏自噬小体;实时荧光定量PCR检测脾脏磷脂酰肌醇3-激酶(PI3K)、蛋白激酶B(Akt)、雷帕霉素靶蛋白(mTOR) mRNA表达水平;Western blot法检测并计算脾脏PI3K、Akt、mTOR蛋白表达及自噬相关蛋白微管相关轻链蛋白3(LC3)、Beclin1、p62蛋白表达。
结果
2
与正常组比较,模型组小鼠体质量、脾脏指数均显著下降(
P
<0.01),脾脏IFN-γ、IL-2含量显著降低(
P
<0.01),脾脏PI3K、Akt、mTOR mRNA及蛋白表达水平均显著下降(
P
<0.01),Beclin1蛋白表达、LC3-II/LC3-I值显著升高(
P
<0.01),p62蛋白表达水平显著下降(
P
<0.01),透射电镜显示脾脏自噬小体数量明显增多,细胞结构损伤程度重。与模型组比较,各药物干预组小鼠上述各指标均显著改善(
P
<0.05或
P
<0.01),健脾补肾方大剂量组小鼠脾脏线粒体可见部分完整脊,自噬体较多;健脾补肾方小剂量组、胸腺肽组小鼠脾脏线粒体结构较完整,自噬体较少。健脾补肾方小剂量组各指标改善效果优于健脾补肾方大剂量组(
P
<0.05或
P
<0.01),且与胸腺肽组各指标差异无统计学意义(
P
>0.05)。
结论
2
健脾补肾方可能通过增强脾脏PI3K/Akt/mTOR信号通路,抑制辐射诱导的自噬过度活化,从而减轻脾脏结构损伤,促进免疫功能的恢复,并以小剂量效佳。
Objective
2
To explore the effects and possible mechanisms of
Jianpi Bushen
Formula
(健脾补肾方) on radiation-induced immune function damage of mice.
Methods
2
Fifty mice were randomly divided into four groups: normal group, model group, thymosin group, high- and low-dose groups of
Jianpi Bushen Formula
, with 10 mice in each group. Except for the normal group, the mice in the other groups were irradiated with a single whole-body dose of 6.0 Gy X-rays to establish a radiation-injured mouse model. After the successful modeling, the low- and high-dose groups of the
Jianpi Bushen Formula
were given respectively 13 g/(kg·d)、 26 g/(kg·d) of the formula by gavage, while the thymosin group was given 11.7 mg/(kg·d) of thymosin by gavage, and the normal group and model group were given 0.1 ml/(10g·d) of 0.9% sodium chloride solution by gavage. Each group was administered once a day for 7 consecutive days. After the last gavage, the mice were weighed, and their spleens were separated and weighed to calculate the spleen index. The levels of interferon gamma (IFN-γ) and interleukin 2 (IL-2) in the spleen tissue were detected by enzyme linked immunosorbent assay (ELISA). The autophagosomes in the spleen were observed by transmission electron microscopy. The mRNA expression levels of phosphatidylinositol 3-kinase (PI3K), protein kinase B (Akt), and mammalian target of rapamycin (mTOR) in the spleen were detected by real-time fluorescent quantitative PCR. The protein expression of PI3K, Akt, and mTOR in the spleen, as well as the expression of autophagy-related proteins microtubule-associated light chain protein 3 (LC3), Beclin1, and p62 were detected by Western blot.
Results
2
Compared with the normal group, the model group showed significant decreases in body weight, spleen index, and levels of IFN-γ and IL-2 in the spleen (
P
<0.01); the mRNA and protein expression levels of PI3K, Akt, and mTOR in the spleen were also significantly reduced (
P
<0.01); the expression of Beclin1 protein, the ratio of LC3-II/LC3-I significantly increased (
P
<0.01), while the level of p62 protein expression significantly decreased (
P
<0.01). And transmission electron microscopy showed a significant increase in the number of autophagosomes in the spleen and severe cell structure damage in the model group. Compared with the model group, all the above indicators in each medication group were significantly improved (
P
<0.05 or
P
<0.01). In the high-dose
Jianpi Bushen Formula
group, partial intact cristae were visible in the fine mitochondria of the spleen, and there were more autophagosomes. In the low-dose
Jianpi Bushen Formula
group and thymosin group, the structure of the fine mitochondria in the spleen was relatively intact, and there were fewer autophagosomes. The improvement effect of the low-dose
Jianpi Bushen Formula
group was better than that of the high-dose group (
P
<0.05 or
P
<0.01), and there was no significant difference between the low-dose group and the thymosin group in terms of each indicator (
P
>0.05).
Conclusion
2
Jianpi Bushen Formula
may alleviate the structural damage of the spleen, promote the recovery of immune function, and achieve a best effect at a low dose by enhancing the PI3K/Akt/mTOR signaling pathway in the spleen and inhibiting the over-activation of autophagy induced by radiation.
LUMNICZKY K , IMPENS N , ARMENGOL G , et al . Low dose ionizing radiation effects on the immune system [J]. Environ Int , 2021 , 149 : 106212 . doi: 10.1016/j.envint. 2020.106212 http://dx.doi.org/10.1016/j.envint.2020.106212 .
郭晗 , 郑全辉 . 自噬在T淋巴细胞中的调控作用 [J]. 中国免疫学杂志 , 2021 , 37 ( 17 ): 2166 - 2169 .
孙睿婕 . 自噬异常在免疫性血小板减少症发病机制中的作用探讨 [D]. 济南 : 山东大学 , 2021 .
YANG J , PI C , WANG G . Inhibition of PI3K/Akt/mTOR pathway by apigenin induces apoptosis and autophagy in hepatocellular carcinoma cells [J]. Biomed Pharmacother , 2018 , 103 : 699 - 707 . doi: 10.1016/j.biopha. 2018. 04. 072 http://dx.doi.org/10.1016/j.biopha.2018.04.072 .
何东初 , 吴江平 , 陈如泉 , 等 . 地甘口服液对肿瘤患者辐射损伤血液和免疫功能的影响 [J]. 中华放射医学与防护杂志 , 2005 , 25 ( 2 ): 139 - 140 .
何东初 , 肖静静 , 林惠 . 健脾补肾方治疗白细胞减少症121例疗效观察 [J]. 中国医药导报 , 2012 , 9 ( 34 ): 101 - 102,107 .
HE DC , XIAO JJ , ZHANG Y , et al . Effect of the Jianpi Bushen Prescription on expressions of the Wnt3a and Cyclin D1 genes in radiation-damaged mice [J]. Genet Mol Res , 2013 , 12 ( 4 ): 4137 - 4146 .
潘琦 , 何东初 , 吴江平 , 等 . 中药复方对辐射损伤小鼠脾细胞凋亡及mRNA表达的影响 [J]. 中华放射医学与防护杂志 , 2003 , 23 ( 5 ): 34 - 35 .
何东初 , 肖静静 , 张梦云 , 等 . 健脾补肾方对辐射损伤小鼠全血细胞及免疫器官的治疗作用研究 [J]. 现代中西医结合杂志 , 2022 , 31 ( 22 ): 3067 - 3073 .
陈奇 . 中药药理研究方法学 [M]. 北京 : 人民卫生出版社 , 1996 : 1103 .
高明泽 , 徐文慧 , 王天琪 , 等 . 急性辐射损伤的中医病因学探讨 [J]. 中医杂志 , 2016 , 57 ( 6 ): 454 - 457 .
ZHENG Y , REN W , ZHANG L , et al . A review of the pharmacological action of astragalus polysaccharide [J]. Front Pharmacol , 2020 , 11 : 349 . doi: 10.3389/fphar. 2020.00349 http://dx.doi.org/10.3389/fphar.2020.00349 .
尤平洪 , 李令勋 , 段小波 , 等 . IL-2、IFN-γ、TNF-α在膀胱癌患者中的水平变化及意义 [J]. 现代生物医学进展 , 2017 , 17 ( 22 ): 4303 - 4306 .
DERETIC V . Autophagy in inflammation, infection, and immunometabolism [J]. Immunity , 2021 , 54 ( 3 ): 437 - 453 .
MIZUSHIMA N , LEVINE B . Autophagy in Human Diseases [J]. N Engl J Med , 2020 , 383 ( 16 ): 1564 - 1576 .
ASHRAFIZADEH M , AHMADI Z , FARKHONDEH T , et al . Autophagy as a molecular target of quercetin underlying its protective effects in human diseases [J]. Arch Physiol Biochem , 2022 , 128 ( 1 ): 200 - 208 .
KLIONSKY DJ , PETRONI G , AMARAVADI RK , et al . Autophagy in major human diseases [J]. EMBO J , 2021 , 40 ( 19 ): e108863 . doi: 10.15252/embj. 2021108863 http://dx.doi.org/10.15252/embj.2021108863 .
MA Y , LI C , HE Y , et al . Beclin-I/LC3-II dependent macroautophagy was uninfluenced in ischemia-challenged vascular endothelial cells [J]. Genes Dis , 2022 , 9 ( 2 ): 549 - 561 .
AGROTIS A , PENGO N , BURDEN JJ , et al . Redundancy of human ATG4 protease isoforms in autophagy and LC3/GABARAP processing revealed in cells [J]. Autophagy , 2019 , 15 ( 6 ): 976 - 997 .
SUN D , WU R , ZHENG J , et al . Polyubiquitin chain- induced p62 phase separation drives autophagic cargo segregation [J]. Cell Res , 2018 , 28 ( 4 ): 405 - 415 .
邹春阳 , 陈晨 , 王凤秋 , 等 . 基于PI3K/Akt/mTOR信号通路的自噬调节剂研究进展 [J]. 中国药物化学杂志 , 2021 , 31 ( 10 ): 825 - 833 .
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