Using Network Pharmacology to Explore Therapeutic Effect of Polygonum capitatum on Renal Calculus in Rats

[Objectives]To explore the therapeutic effect of Polygonum capitatum on renal calculus in rats based on network pharmacology.[Methods]Through the preliminary construction of P.capitatum-urolithiasis disease target network,explore the active components,action pathway and action target of P.capitatum-urolithiasis treatment,and use 1%ethylene glycol+2%ammonium chloride to induce SD rat kidney calcium oxalate stone model to verify the efficacy of P.capitatum-urolithiasis treatment.[Results]Through the network pharmacological prediction,it is found that the important active components in P.capitatum were quercetin,gallic acid,rutin,silybin,catechin,kaempferol and so on;potential active targets include INS,CAT,IL-6,MOCOS,etc.The results also suggest that forkhead transcription factor signaling pathway(FoxO signaling pathway),tumor necrosis factor signaling pathway(TNF signaling pathway)and hypoxia-inducible factor signaling pathway(HIF-1 signaling pathway)are the core pathways.The results of biochemical indicators in animal experiment showed that the contents of serum urea nitrogen(BUN),creatinine(Cr)and malondialdehyde(MDA)in renal tissue in the treatment group(200,500 mg/kg)were significantly lower than those in the model group,while the content of superoxide dismutase(SOD)was significantly higher than that in the model group.In addition,the kidney tissue H&E staining sections showed that P.capitatum alcohol extract administration group rats kidney calcium oxalate crystals were significantly reduced compared with the model group,the degree of renal tubular lumen expansion was lighter than the model group,suggesting that P.capitatum alcohol extract has the effect of improving renal calculus in rats.[Conclusions]This study provides a theoretical reference for the deep development of P.capitatum in the treatment of renal calculus.

A New Flavonoid Glycoside from Polygonum capitatum

[Objectives]To discover novel compounds with significant anti-inflammatory activity in the alcohol extract of Polygonum capitatum.[Methods]Firstly,a new flavonoid glycoside,capitaone B(1),was isolated from the ethyl acetate extract from P.capitatum,and then 27 compounds were screened using NO anti-inflammatory activity model.[Results]Four compounds,such as kaempferol(12),1,2,6-trigalloyl-β-d-glucose(15),catechin(16)andβ-sitosterol(26),could significantly inhibit LPS-induced NO production in macrophages,with IC 50 values of 15.31,8.43,6.92 and 5.72μM,respectively.[Conclusions]The chemical composition and anti-inflammatory activity of P.capitatum were preliminarily studied,and the results provide a theoretical basis for further research on the action mechanism of subsequent anti-inflammatory active compounds of P.capitatum.

In vivo recognition of bioactive substances of Polygonum multiflorum for protecting mitochondria against metabolic dysfunction-associated fatty liver disease

BACKGROUND Metabolic dysfunction-associated fatty liver disease(MAFLD)is a severe threat to human health.Polygonum multiflorum(PM)has been proven to remedy mitochondria and relieve MAFLD,but the main pharmacodynamic ingredients for mitigating MAFLD remain unclear.AIM To research the active ingredients of PM adjusting mitochondria to relieve highfat diet(HFD)-induced MAFLD in rats.METHODS Fat emulsion-induced L02 adipocyte model and HFD-induced MAFLD rat model were used to investigate the anti-MAFLD ability of PM and explore their action mechanisms.The adipocyte model was also applied to evaluate the activities of PM-derived constituents in liver mitochondria from HFD-fed rats(mitochondrial pharmacology).PM-derived constituents in liver mitochondria were confirmed by ultra-high-performance liquid chromatography/mass spectrometry(mitochondrial pharmacochemistry).The abilities of PM-derived monomer and monomer groups were evaluated by the adipocyte model and MAFLD mouse model,respectively.RESULTS PM repaired mitochondrial ultrastructure and prevented oxidative stress and energy production disorder of liver mitochondria to mitigate fat emulsion-induced cellular steatosis and HFD-induced MAFLD.PM-derived constituents that entered the liver mitochondria inhibited oxidative stress damage and improved energy production against cellular steatosis.Eight chemicals were found in the liver mitochondria of PM-administrated rats.The anti-steatosis ability of one monomer and the anti-MAFLD activity of the monomer group were validated.CONCLUSION PM restored mitochondrial structure and function and alleviated MAFLD,which may be associated with the remedy of oxidative stress and energy production.The identified eight chemicals may be the main bioactive ingredients in PM that adjusted mitochondria to prevent MAFLD.Thus,PM provides a new approach to prevent MAFLD-related mitochondrial dysfunction.Mitochondrial pharmacology and pharmacochemistry further showed efficient strategies for determining the bioactive ingredients of Chinese medicines that adjust mitochondria to prevent diseases.

Systematic Evaluation of Pharmacognostic Identification of Polygonum capitatum

[Objectives] To investigate the systematic evaluation of pharmacognostic identification of Polygonum capitatum . [Methods] 10 batches of P. capitatum cultivated in Guizhou were chosen for plant samples. Macroscopical identification was conducted on plant roots, stems, leaves, flowers and fruits. The P. capitatum powder was processed for physical and chemical distinction by FeCl 3 chromogenic reaction, hydrochloric acid magnesium powder reaction, AlCl 3 color development reaction and thin-layer chromatography.Microscope identification was carried out on the powder. Plant genome DNeasy Plant Kit was adopted for DNA molecular marker identification. [Results] The results showed that the stem of P. capitatum was tufted, the leaves were oval, 2 to 5 cm long, and 1 to 2 cm wide;the leaf apex was acute and cuneate at the base, the inflorescence was capitate, paired or solitary;the raceme was erect and nearly spherical, and the perianth was light red. Furthermore, for the chromogenic reaction of FeCl 3 ethanol extract of P. capitatum , appeared blue and turned to dark blue after long time storing at room temperature. For the reaction of hydrochloric acid magnesium powder, the alcohol extract of P. capitatum , exhibited deep red. In the color reaction of AlCl 3, the alcohol extract revealed yellow fluorescence under 360 nm UV lamp. Microscope identification of the powder displayed pollen grains, crystal sheath fibers, cellulose, vessels, starch grains, cork cells, and other characteristic fragments. In addition, DNA barcoding electrophoresis results showed that P. capitatum showed a clear and bright single band near 500 bp, and further sequencing results showed that the sequence differences were mainly concentrated in ITS1 and ITS2 region. [Conclusions] Systematic evaluation for the identification of P. capitatum is established, which combines with macroscopic identification, physicochemical identification, powder microscope identification, and DNA molecular identification. Finally, the original medicinal material is identified as P. capitatum Buch.-Ham. ex D. Don.

Effects of Polygonatum sibiricum Polysaccharide on Antioxidant Capacity of the Liver in High-fat Diet Rats

[Objectives]This study was conducted to investigate the effects of Polygonatum sibiricum polysaccharide(PSP)on antioxidant function in high-fat diet obese rats.[Methods]Thirty five healthy male SD rats were selected to establish an obesity model after feeding a high-fat for 8 weeks.They were then randomly divided into a normal group(NC),a high-fat diet group(HF),and an HF+P.sibiricum polysaccharide group[HF+PSP,300 mg/(kg·d)].After 6 weeks of PSP intervention,the serum and liver of rats were collected,and the activity of aspartate transaminase(AST)and alanine aminotransferase(ALT)in serum,the enzyme activity of superoxide dismutase(SOD),catalase(CAT)and glutathione peroxidase(GSH-Px)and malondialdehyde(MDA)in liver tissue were measured.The pathological changes of liver tissue were observed by HE staining.[Results]Compared with the HF group,PSP could effectively inhibit obesity caused by high-fat diet.It reduced body weight and serum AST and ALT levels,increased the contents of T-SOD,CAT and GSH-Px in the liver,and inhibited the accumulation of MDA content,thereby reducing damage to liver cells caused by a high-fat diet.It indicated that PSP could effectively inhibit obesity in high-fat diet rats and enhance their antioxidant capacity.[Conclusions]This study provides a reference for the study of the antioxidant capacity of PSP.

Antioxidant,Anti-inflammatory,and Antibacterial Activities of Different Extracts from Polygonum capitatum

[Objectives]To investigate the antioxidant,anti-inflammatory and antibacterial activities of different extracts(aqueous,ethanol,ethyl acetate and n-butanol extracts)of Miao medicine Polygonum capitatum.[Methods]Eleven batches of P.capitatum in Guizhou province were collected,and water,ethanol,ethyl acetate and n-butanol extracts were prepared by reflux extraction.Antioxidant activity was determined by radical scavenging capacity of 1,1 diphenyl-2-picyl hydrazine(DPPH),anti-inflammatory activity was screened by lipopolysaccharide(LPS)induced RAW264.7 cells to produce NO,and the minimum inhibitory concentration(MIC)was screened by broth microdilution method.[Results]When the concentration of ethyl acetate extract was 10 mg/L,the scavenging rate of DPPH ranged from 90%to 99%.The(MIC of the ethyl acetate extract against Staphylococcus aureus(SA),Pseudomonas aeruginosa(PA)and Escherichia coli(EC)was 0.18-0.65,0.13-0.82,and 0.15-0.78 g/L,respectively.In the anti-inflammatory activity,ethyl acetate extract inhibited NO production with inhibition rate of 70%.[Conclusions]The ethyl acetate extract and ethanol extract of Miao medicine P.capitatum have strong antioxidant,anti-inflammatory and antibacterial activities.

九蒸九制对黄精中AGEs含量、多糖结构及体外活性的影响

为初步判断九蒸九制黄精多糖含量下降的主要原因及九蒸九制对黄精多糖体外活性的影响,本文测定了九蒸九制黄精中5-羟甲基糠醛(5-HMF)及晚期糖基化终产物(AGEs)的含量,考察了九蒸九制前后黄精纯化多糖的结构变化,并分析这些变化对黄精体外活性的影响。结果表明九蒸九制黄精发生了美拉德反应,5-HMF含量为(631.3±21.5)μg/g,羧甲基赖氨酸(CML)和羧乙基赖氨酸(CEL)含量分别为(342.4±11.3)μg/g和(63.7±9.8)μg/g。并对黄精多糖的结构及组成产生了不同程度的影响,葡萄糖(Glc)含量有所增长,甘露糖(Man)及半乳糖醛酸(GalUA)的含量有明显降低,Man从34.53%降至17.06%,GalUA从9.59%降至1.77%。研究表明,黄精在九蒸九制的加工过程中发生了美拉德反应,并产生了一定量的AGEs,同时,九蒸九制法在一定程度提高了黄精多糖的体外降糖活性。

何首乌叶不同萃取物的抗炎活性及其化学成分鉴定

目的:研究何首乌叶的成分,为其功能食品的研发提供基础数据。方法:对何首乌叶醇提取物进行有机溶剂萃取,分别得到何首乌叶石油醚、二氯甲烷、乙酸乙酯、正丁醇、水等不同萃取物,并对不同萃取物进行抗炎活性检测,后续通过硅胶柱色谱、C18柱色谱结合半制备液相等方法对抗炎活性较好的成分进行分离、纯化以及结构鉴定,结果:在质量浓度0~100μg/mL范围内,乙酸乙酯萃取物对RAW264.7细胞存活率无明显的抑制作用,且剂量依赖地抑制NO的生成。石油醚和二氯甲烷萃取物在质量浓度0~25μg/mL时,均无明显细胞毒性,并在25μg/mL时,二氯甲烷萃取物对NO的抑制率(51.47%)高于石油醚萃取物的抑制率(43.91%)。从二氯甲烷和乙酸乙酯萃取物中分离、鉴定出11个化合物,分别为2,3,4,6-三羟基苯乙酮-3-O-β-D-glucoside(1)、杨梅苷(2)、槲皮苷(3)、阿福豆苷(4)、β-谷甾醇(5)、正十六烷-5,8,11三烯酸(6)、二十六烷(7)、α-亚麻酸(8)、山柰酚-3-O-芸香糖苷(9)、肉豆蔻酸(10)和槲皮素(11)。结论:何首乌叶具有很好的抗炎活性,化合物2,4,6,7,8,9,10,11均为首次从何首乌中分离得到。

黄精黑糯米酒酿造工艺优化及其品质分析

以黑糯米为主要原料,黄精提取液为辅料制备黄精黑糯米酒。以感官评分为评价指标,通过单因素试验和正交试验优化液态法发酵黄精黑糯米酒酿造工艺条件,并对其理化指标及活性成分进行测定。结果表明,最佳酿造工艺条件为酒曲与酵母质量比1:1、发酵时间6 d、黄精提取液添加量28%、料液比(糯米与水)1.0:7.0(g:mL)。在此优化条件下,黄精黑糯米酒的酒体澄清透亮、呈紫红色、酒香醇厚、具有黄精风味,感官评分为87分,酒精度达12.0%vol,总糖、还原糖、总酸、氨基酸态氮、花色苷和总黄酮含量分别为4.13 g/100 mL、3.74 g/100 mL、6.32 g/L、0.22 g/L、37.9 mg/L、0.023 g/100 mL。

HPLC法同时测定杠板归不同部位中5种成分的含量

目的建立高效液相色谱法同时测定杠板归不同部位(茎、叶、根)中5种成分的含量。方法采用Luna?-C18(4.6 mm×250 mm,5μm)色谱柱,以乙腈-0.1%磷酸水为流动相梯度洗脱,流速为1.0 mL/min,检测波长为320 nm,柱温为30℃,测定杠板归不同部位中绿原酸、咖啡酸、芦丁、阿魏酸、槲皮素的含量。结果绿原酸、咖啡酸、芦丁、阿魏酸、槲皮素分别在0.046~4.6μg/mL,0.212~21.2μg/mL,0.055~5.5μg/mL,0.084~8.4μg/mL,0.114~11.4μg/mL范围内质量浓度与峰面积呈线性关系良好(r>0.9990),平均加样回收率为97.65%~102.09%,RSD为1.76%~2.44%。不同部位中5种成分含量差异较大,绿原酸和咖啡酸2个成分在叶中含量高,且远远高于根和茎中的含量;芦丁和阿魏酸主要存在于茎和根中,叶中未检测到;槲皮素在茎中含量最高,叶中次之,根中最低。结论建立的HPLC方法准确可靠、重复性好、专属性强,可用于杠板归不同部位中5个成分含量的同时测定。

苗药花蝴蝶回调CIA模型鼠血细胞变化的初步研究

目的 观察苗药花蝴蝶回调胶原诱导关节炎(CIA)模型鼠外周血细胞变化的初步作用机制。方法 40只大鼠随机分为花蝴蝶低剂量治疗组(花蝴蝶低组)、花蝴蝶高剂量治疗组(花蝴蝶高组)、甲氨蝶呤治疗组(甲氨蝶呤组)、CIA模型组(模型组)和正常组,分别按相关文献资料并结合民间用药经验灌胃给药。观察大鼠足关节肿胀度,检测大鼠外周血白细胞计数、淋巴细胞计数、单核细胞计数、淋巴细胞/单核细胞、红细胞计数、血细胞比容、血小板计数和平均血小板体积等指标,研究大鼠足关节病理切片等。结果 模型组大鼠足关节肿胀指数评分明显高于花蝴蝶低组、花蝴蝶高组、甲氨蝶呤组和正常组(P<0.01);正常组、甲氨蝶呤组、花蝴蝶高组、花蝴蝶低组足关节肿胀指数评分各组间比较差异无统计学意义(P>0.05)。与其他各组比较,模型组大鼠外周血白细胞计数、淋巴细胞计数、单核细胞计数、红细胞计数、血细胞比容、血小板计数均明显升高,而模型组大鼠外周血淋巴细胞/单核细胞、平均血小板体积均降低(P<0.01)。正常组、甲氨蝶呤组、花蝴蝶高组、花蝴蝶低组外周血相关检测指标各组间比较差异无统计学意义(P>0.05)。与其他各组比较,模型组大鼠膝关节骨髓腔淋巴细胞、单核细胞评分升高,而脂肪细胞评分降低(P<0.01)。正常组、甲氨蝶呤组、花蝴蝶高组、花蝴蝶低组大鼠膝关节骨髓腔淋巴细胞、单核细胞和脂肪细胞评分各组间比较差异无统计学意义(P>0.05)。结论 苗药花蝴蝶可能通过回调骨髓淋巴细胞、单核细胞、红细胞、血细胞比容、血小板等指标升高和平均血小板体积、淋巴细胞/单核细胞比值降低,回转CIA模型鼠外周血相应血细胞变化,最终缓解CIA模型鼠症状,这可能是苗药花蝴蝶治疗类风湿关节炎的初步作用机制之一。

陕西省黄精生态种植模式评价与技术分析

以陕西省黄精为研究对象,对其在陕西省的生态种植技术进行系统分析与评价。结果表明,在陕西省黄精的种植模式主要分为2种,林下种植与间套作种植模式。林下种植黄精可有效利用陕西省土地资源且可形成良好的生态环境。黄精的间套作模式为黄精的生长创造了良好的根际环境,同时改善了农业生态环境,促进了资源再生和循环利用。

固态发酵制备黄精多糖的工艺优化、理化特性及抗氧化活性

选取7种乳杆菌进行固态发酵,以黄精多糖得率为评价指标确定最佳发酵菌种。借助单因素试验和响应面曲面分析法对固态发酵黄精工艺进行优化,并分析固态发酵黄精多糖(solid state fermentation Polygonatum sibiricum polysaccharide,SF-PSP)与相同条件下未经发酵黄精多糖(P.sibiricum polysaccharide,PSP)的单糖组成、形态特征、热失重特性以及体外抗氧化活性。结果表明:副干酪乳杆菌ATCC 334为最优发酵菌种,SF-PSP的最佳制备工艺条件为:液料比0.98∶1(mL∶g)、接菌量4.80%、发酵时间51.30 h,此条件下SF-PSP得率为(11.14±0.89)%。SF-PSP主要由甘露糖、半乳糖醛酸、半乳糖和葡萄糖组成,与PSP相比,鼠李糖、半乳糖醛酸、半乳糖含量均提高了4倍。扫描电镜结果表明,与PSP相比,SF-PSP结构更加疏松且有更多致密的小孔。热重分析结果表明2种多糖失重温度节点不同,且SF-PSP保水能力优于PSP。体外抗氧化活性结果表明SF-PSP的DPPH自由基清除率、ABTS阳离子自由基清除率、亚铁离子螯合能力及总抗氧化性均显著高于PSP(P<0.05)。综上,采用SF-PSP可以显著提高黄精多糖的得率和抗氧化活性。

九蒸九制对鸡头黄精理化性质及抗氧化性的影响

为了探究蒸制处理对鸡头黄精有效成分及代谢物种类和含量影响,采用低场核磁、苯酚-浓硫酸法、高效液相色谱-蒸发光散射检测法(HPLC-ELSD)和液相色谱-质谱技术(LC-MS)等对其中的水分分布、多糖含量、单糖组成和代谢产物等进行分析。结果表明,多次蒸制后,鸡头黄精结合水的含量、多糖含量逐渐降低,水提液pH值逐渐降低呈弱酸性达到4.07,还原糖、总酚、黄酮含量逐渐升高分别达到28.69%、10.02 mg/g和0.69%,抗氧化性逐渐增强,ABTS抗氧化能力在7制达到最高为0.73 mmol/L,较1制增加0.35 mmol/L,DPPH自由基清除率和FRAP值在8制达到最高分别为81.95%,1.97 mmol/L,较1制分别增加50.92%,1.72 mmol/L;同时蔗糖逐渐水解从18.53mg/g到7.62mg/g,葡萄糖和果糖含量提高,分别由1制0.00和11.30mg/g,达到9制17.25和230.89 mg/g。选取一制与九制黄精进行代谢物差异分析,在正离子模式下共检测到1310种代谢物,差异代谢物有176种(按其特性分为38类),在负离子模式下共检测到1841种代谢物,差异代谢物有148种(按其特性分为26类)。黄精经蒸制后有效成分差异性显著,对鸡头黄精炮制加工提供科学依据。

两种同属食药同源植物黄精与玉竹代谢组学比较分析

采用代谢组学方法比较分析了同属食药同源植物黄精和玉竹代谢物质的组成及差异。利用基于超高效液相色谱-质谱联用技术(UHPLC-MS)的非靶向代谢组学技术,对黄精与玉竹的根部进行了分析。两种中药共检测到583个差异代谢物,玉竹与黄精相比,其中共有536个代谢物含量显著上升,47个代谢物含量显著下降。在这些代谢物中,有150种黄酮类化合物在黄精和玉竹中存在显著性差异,其中:139种显著上调,11种显著下调。甾体皂苷类化合物在黄精和玉竹中共检测到110种,其中:93种显著上调,17种显著下调。生物碱类化合物在黄精和玉竹中共检测到73种,其中:61种显著上调,12种显著下调。98种酚酸类化合物在黄精与玉竹中存在显著性差异,其中:96种显著上调,2种显著下调。48种萜类化合物在黄精与玉竹中存在显著性差异,其中:47种显著上调,1种显著下调。这些研究结果可为黄精与玉竹的开发研究提供理论依据。

人工湿地园沼泽植物水蓼(Polygonum hydropiper L.)的蒸腾特性日变化

对人工湿地园中沼泽植物水蓼(PolygonumhydropiperL.)蒸腾特性日变化进行了研究。结果表明:水蓼叶片的蒸腾速率日进程在晴朗的天气呈单峰曲线变化,最高峰值出现在下午的14:00。受光量子通量密度的影响最大,相关系数为0.668。与相对湿度的变化呈正相关(r=0.607),说明水蓼的蒸腾速率日变化是受其自身所具有的特殊生理特性所决定。叶片气孔阻力直接影响蒸腾速率。

广西产火炭母总黄酮提取工艺优化及含量测定

采用紫外可见分光光度法测定火炭母(Polygonum chinense L.)中总黄酮的含量,以总黄酮含量为考察指标,以提取方式、提取溶剂、料液比、提取时间、提取次数为考察因素,在单因素试验的基础上,采用L9(33)正交设计优化火炭母中总黄酮的提取工艺。最优提取工艺:70%乙醇为提取溶剂,料液比1∶70(m/V),超声波提取45 min,提取2次。以芦丁为对照品,在500 nm波长处测定其吸光度,平均加样回收率为98.76%,相对标准偏差为1.72%。结果表明,13个产地火炭母药材的总黄酮含量为22.205 4~52.173 7 mg/g,相对标准偏差(RSD)为1.07%~2.81%。13个产地总黄酮含量由高到低依次为桂林市、南宁市、玉林市、百色市、贺州市、河池市、贵港市、防城港市、钦州市、梧州市、来宾市、崇左市、柳州市。该方法精密度、稳定性、重复性良好,可作为广西产火炭母药材质量评价的依据。

黄精施肥与栽培模式研究进展

黄精是药食两用的中药材,具有润肺滋肾、补脾益气的功效。由于市场需求量增长较快,野生黄精资源已经不能满足市场需求,促使人工栽培黄精规模不断扩大。科学合理的施肥方法可以促进中药材的生长发育,从而增加中药材产出。基于已有研究,综述黄精施肥及栽培模式,分析目前存在的问题并提出建议,以期为今后黄精的开发和利用提供参考。

Mn对超富集植物短毛蓼(Polygonum pubescens Blume)抗氧化机理的影响

采用水培的方法,研究了不同浓度Mn(0、0.5、1、2、4、8mmol·L-1)对新发现的Mn超富集植物短毛蓼(Polygonum pubescens Blume)生长、Mn吸收及Mn对其抗氧化酶和非酶系统的影响。结果表明,锰处理显著增加了(P<0.05)短毛蓼根、茎、叶中Mn的含量,锰处理还引起了短毛蓼叶片中过氧化氢(H2O2)和丙二醛(MDA)的累积。当Mn处理浓度大于1mmol·L-1时,显著降低了短毛蓼的株高、株重(P<0.05);当Mn处理浓度为8mmol·L-1时,短毛蓼叶片中叶绿素a、叶绿素b、叶绿素a+b含量最低,与对照差异显著(P<0.05)。Mn处理显著提高了短毛蓼叶片中超氧物歧化酶(SOD)活性(P<0.05),而过氧化物酶(POD)、过氧化氢酶(CAT)和抗坏血酸过氧化物酶(APX)的活性呈先升后降趋势,表明Mn处理打破了短毛蓼活性氧物质的正常代谢,并启动了抗氧化酶系统。8mmol·L-1的Mn处理,显著提高了短毛蓼叶片中巯基(-SH)、还原型谷胱甘肽(GSH)的含量(P<0.05),比对照分别提高了10.6%和20%,表明-SH、GSH在短毛蓼缓解Mn毒害的过程中起着重要作用。

基于trnL-F序列探讨杠板归Polygonum perfoliatum的系统位置

杠板归(Polygonum perfoliatum L.)的系统位置一直存在争议,文中以塔黄为外类群,采用最大简约法对杠板归及其近缘类群的trnL-F序列进行了系统发育分析,结果表明:(1)杠板归和刺蓼为姊妹群,自展分析的支持率为99%,分子证据支持杠板归归入刺蓼组,而没有必要单立组或属。(2)刺蓼组、春蓼组和头状蓼组植物聚在一起,自展支持率为100%,说明它们之间有很近的亲缘关系。