A comprehensive insight into potential roles of Nigella sativa on diseases by targeting AMP-activated protein kinase: a review

ObjectivesNigella sativa (NS) is a known medicinal herb with numerous therapeutic effects such as antidiabetic, anti-proliferative, anti-inflammatory, and anti-cancer activities. It has been indicated that NS can regulate cellular metabolism by adjusting transduction signaling pathways. Adenosine monophosphate-activated protein kinase (AMPK) is one of the main physiological processes, such as energy hemostasis, cellular metabolism, and autophagy regulators. Herb-derived medicines have always been considered as one of the main AMPK activators, and surprisingly recent data has demonstrated that it can be a target for NS and its derivatives.Evidence acquisitionThe literature search was conducted in PubMed, SCOPUS, Embase, ProQuest, and Google Scholar electronic resources. Published articles up to September 2020 were considered, and those of which investigated Nigella sativa effects on the AMPK pathway after meeting the inclusion criteria were included.ResultsThe search was performed on several online databases such as PubMed, Scopus, Embase, ProQuest, and Google Scholar from inception until January 2020. Among the initial search, 245 studies were found. After removing duplicated data and meeting the inclusion criteria, only 14 studies were selected. They included the effects of NS and its bioactive compounds as anti-hyperglycemic (n = 5), on liver function (n = 4), cancers (n = 3), and on Neuroinflammation and Atherosclerosis (n = 2). Most of the included studies are animals or in-vitro investigations.ConclusionIn this review, we discuss the latest findings on the molecular mechanism of NS effecting the AMPK signaling pathway. We also focus on the therapeutic effects of NS, including the prevention and treatment of metabolic and pro-inflammatory disease by targeting the AMPK pathway.Graphical abstract     

综合疗法治疗4~5期慢性肾脏病31例临床观察

目的:观察综合疗法治疗慢性肾脏病(CKD)4~5期脾肾亏虚证的效果。方法:将CKD4~5期脾肾亏虚证患者62例随机分为2组,其中治疗组31例,对照组30例(剔除1例)。对照组予基础治疗合中药、骨化三醇及碳酸钙D3片治疗,治疗组予基础治疗合中药、骨化三醇及益肾泄浊汤保留灌肠治疗,观察时间为4周。比较2组血肌酐(Scr)、肾小球滤过率(e GFR)、尿素氮(BUN)、血钙、血磷、碱性磷酸酶(ALP)、甲状旁腺激素(i PTH)及中医证候疗效。结果:中医证候总有效率治疗组为83.87%(26/31),对照组为73.33%(22/30),组间比较,差异有统计学意义(P<0.05);2组Scr、e GFR、BUN、血磷治疗前后组内比较及治疗后组间比较,差异均有统计学意义(P<0.01或P<0.05);2组血钙、i PTH、ALP治疗前后组内比较,差异均有统计学意义(P<0.01),但治疗后组间比较,差异无统计学意义(P>0.05)。结论:综合疗法治疗慢性肾脏病4~5期脾肾亏虚证效果确切,安全可靠。     

从脾论治慢性肾脏病的生物学基础探讨

脾为后天之源,肾为先天之本,以后天滋先天,使从脾论治成为中医临床治疗慢性肾脏病(CKD)的经典方法。现代医学研究发现人体内最庞大的“器官”——肠道菌群与“脾”的功能非常密切。目前研究发现肠道菌群紊乱是加速CKD进展的重要环节,基于脾肾互根互用的中医原理,收集、整理肠道菌群与CKD代谢功能、免疫应答及肾脏损伤关联的文献,从肠道菌群与机体功能代谢和内环境稳态的角度进行探讨,认识到运用中医药可通过干预肠道菌群的丰度、结构和代谢功能,维持肠道微生态的平衡,从而达到调节肾脏代谢和免疫应答的作用,提出肠道菌群是从脾论治慢性肾脏病的重要生物学基础。     

中药口服对经内镜摘除后大肠腺瘤 防治作用的Meta分析

目的：评价中药口服对经内镜摘除后大肠腺瘤的防治作用。方法：搜索Pubmed、Embase、Web of science、CBM、万方数据库、中国知网、维普数据库、Cochrane Library中关于中医药防治大肠腺瘤息肉术后的临床随机对照实验的文献。对纳入文献进行筛选、提取，评估，运用Review Manager 5.3软件进行Meta分析。结果：共纳入13篇文献，1 103例患者，以临床有效率为观察指标的有5篇，异质性检验Chi2=0.67、df=4（P=0.96)、I2=0%，使用固定效应模型统计OR=3.56，95%CI：［2.03,6.23］,Z=4.45（P<0.000 01），观察组优于对照组，2组临床疗效差异有统计学意义。以半年复发率为观察指标的有10篇，异质性检验Chi2=9.26、df=9（P=0.41)、I2=3%，使用固定效应模型合并统计量OR=3.29，95%CI：［2.30,4.69］,Z=6.54（P<0.000 01），观察组复发率低于对照组，差异有统计学意义；以1年复发率为观察指标的有7篇，异质性检验Chi2=6.01、df=6（P=0.42)、I2=3%，使用固定效应模型合并统计量OR=4.21，95%CI：［2.88,6.16］,Z=7.41（P<0.000 01），观察组复发率低于对照组，差异有统计学意义。结论：中药口服对降低内镜下切除大肠腺瘤复发率有效，同时改善术后腹痛腹泻症状，以参苓白术散加减为代表的健脾方药具有良好的临床疗效。     

银杏内酯B对肌萎缩侧索硬化细胞模型的保护作用及其机制

目的:探讨银杏内酯B(ginkgolide B,GB)对肌萎缩侧索硬化细胞模型c-Jun氨基末端激酶(JNK)信号通路及细胞凋亡的影响。方法:通过含过表达人突变超氧化物歧化酶1(SOD1)~(G93A)基因(hSOD1~(G93A))和过表达人野生SODWT基因(hSOD1WT)与空质粒的慢病毒感染NSC34细胞,经一定浓度的嘌呤霉素筛选,倒置荧光显微镜下观察慢病毒的转染效率和细胞形态的变化,蛋白免疫印迹法(Western blot)检验感染细胞是否过表达SOD1蛋白,建立hSOD1~(G93A)-NSC34细胞系后给予GB,细胞培养分组为正常组、模型组、不同浓度GB组(25,50,75,100 mg·L-1)组,48 h后噻唑蓝(MTT)比色法检测细胞存活率,筛选出最佳药物浓度,后续实验分组为以正常组,模型组,75 mg?L~(-1) GB组,SP600125组,75 mg?L-1GB+SP600125组,流式细胞术检测各组细胞的凋亡率,蛋白免疫印迹法(Western blot)检测磷酸化(p-)JNK,c-Jun,p-c-Jun,半胱氨酸天冬氨酸蛋白酶-3(Caspase-3)蛋白的表达。结果:与正常的NSC34细胞比较,hSOD1~(G93A)NSC34组细胞胞体变圆,突触减少、变短,而hSOD1WT NSC34组细胞和空质粒组细胞形态学未发生明显变化,与正常组比较,hSOD1~(G93A)NSC34组,hSOD1WTNSC3组细胞内SOD1蛋白水平显著升高(P0. 01),肌萎缩侧索硬化(ALS)细胞模型成功建立。与正常组比较,模型组细胞存活率显著降低(P0. 01);与模型组比较,给予不同浓度GB后,细胞存活率均显著升高(P0. 01),药物质量浓度为75 mg?L-1时细胞存活率显著升高(P0. 01)。后续实验,与正常组比较,模型组凋亡率,p-JNK,p-c-Jun,cleaved Caspase-3蛋白表达量显著升高(P0. 01);与模型组比较,75 mg?L-1GB组,SP600125组,75 mg?L-1GB+SP600125组凋亡率,p-JNK,p-c-Jun,cleaved Caspase-3蛋白表达明显降低(P0. 05,P0. 01)。结论:GB对肌萎缩侧索硬化细胞模型具有抑制细胞凋亡的保护作用,这种保护作用可能是通过JNK信号通路实现的。     

观察疏肝健脾法治疗月经不调的临床治疗效果及相应的护理观察

目的:探讨疏肝健脾法治疗月经不调的临床治疗效果,并总结相应护理方法。方法:选取自2017年9月-2018年9月在日照市中医医院接受诊疗的136例肝郁脾虚型月经不调患者随机分为对照组和研究组,对照组行逍遥丸治疗,并给予常规护理;研究组行逍遥散、参苓白术散治疗,并给予针对性护理,比较两组患者的治疗效果与护理满意度。结果:研究组治疗总有效率为91.18%(62/68),明显高于对照组的66.18%(45/68)(P<0.05);研究组患者护理满意率为94.12%(64/68),明显高于对照组的76.47%(52/68)(P<0.05)。结论:针对肝郁脾虚型月经不调患者,采取疏肝健脾法进行治疗具确切临床疗效,辅以针对性护理,还能提高患者护理满意度,值得推广应用。     

EGFR敏感突变晚期非小细胞肺癌一线治疗研究进展

分子靶向治疗是在驱动基因指导下的治疗，开启了非小细胞肺癌“个体化”与“精准”治疗时代。非小细胞肺癌驱动基因包括表皮生长因子受体（EGFR）、间变淋巴瘤激酶（ALK）和原癌基因-1（Ros-1）等。EGFR 突变是非小细胞肺癌最常见的靶点，表皮生长因子受体-酪氨酸激酶抑制剂（EGFR-TKI）是治疗EGFR 突变晚期非小细胞肺癌的最有效药物，已广泛用于临床治疗，但后期耐药问题不可避免。近年来，为优化TKI 治疗，EGFR-TKI 联合治疗应运而生，不断探索有效的EGFR-TKI 联合治疗的方案。如EGFR-TKI 联合抗血管生成药物、化疗和免疫治疗等。本文就一线EGFR-TKI 药物及EGFR-TKI 联合治疗在一线探索的有关临床研究进展进行综述。     

重灸中脘穴对脾胃虚寒型糖尿病胃轻瘫患者胃肠激素、胃动力学的影响

目的观察重灸中脘穴对脾胃虚寒型2型糖尿病胃轻瘫患者胃肠激素、胃动力学的影响。方法选取符合纳入标准的88例脾胃虚寒型糖尿病胃轻瘫患者,按随机数字表法分为治疗组和对照组,每组44例。对照组采用常规药物治疗,治疗组采用重灸中脘穴治疗。疗程结束后记录并对比分析两组临床疗效、胃肠激素[胃泌素(GAS)、胃动素(MTL)]、胃动力学(胃收缩频率、胃排空时间、胃排空率)、主要临床症状评分等变化。结果治疗组临床疗效明显优于对照组,差异具有统计学意义(P<0.05);两组治疗后GAS、MTL均明显优于治疗前(P<0.05),且治疗组明显优于对照组(P<0.05);两组治疗后胃收缩频率、胃排空时间、胃排空率均明显优于治疗前(P<0.05),且治疗组明显优于对照组(P<0.05);两组治疗后主要临床症状评分均明显优于治疗前(P<0.05),且治疗组明显优于对照组(P<0.05)。结论在常规药物治疗基础上重灸中脘穴治疗脾胃虚寒型2型糖尿病胃轻瘫,可调节胃肠激素,改善胃肠动力,促进胃肠功能恢复。     

Deoxyelephantopin decreases the release of inflammatory cytokines in macrophage associated with attenuation of aerobic glycolysis via modulation of PKM2

Growing evidence suggests that activated immune cells undergo metabolic reprogramming in the regulation of the innate inflammatory response. Remarkably, macrophages activated by lipopolysaccharide (LPS) induce a switch from oxidative phosphorylation to aerobic glycolysis, and consequently results in release of proinflammatory cytokines. Pyruvate Kinase M2 (PKM2) plays a vital role in the process of macrophage activation, promoting the inflammatory response in sepsis and septic shock. Deoxyelephantopin (DET), a naturally occurring sesquiterpene lactone from Elephantopus scaber, has been shown to counteracts inflammation during fulminant hepatitis progression, but the underlying mechanism remains unclear. Here, we studied the function of the DET on macrophage activation and investigated the anti-inflammatory effects of DET associated with interfering with glycolysis in macrophage. Our results first demonstrated that DET attenuates LPS-induced interleukin-1β (IL-1β) and high-mobility group box 1 (HMGB1) release in vitro and in vivo and protected mice against lethal endotoxemia. Furthermore, DET decreased the expression of pyruvate dehydrogenase kinase 1 (PDK1), glucose transporter 1(GLUT1), lactate dehydrogenase A (LDHA), and reduced lactate production dose-dependently in macrophages. Moreover, we further revealed that DET attenuates aerobic glycolysis in macrophages associated with regulating the nuclear localization of PKM2. Our results provided a novel mechanism for DET suppression of macrophages activation implicated in anti-inflammatory therapy.