Scientia Agricultura Sinica ›› 2023, Vol. 56 ›› Issue (5): 981-994.doi: 10.3864/j.issn.0578-1752.2023.05.013

• FOOD SCIENCE AND ENGINEERING • Previous Articles     Next Articles

Lipid-Lowering Effects and Its Regulation Mechanism of Buckwheat Polyphenols in High-Fat Diet-Induced Obese Mice

YAO YiJun(), JU XingRong, WANG LiFeng()   

  1. College of Food Science and Engineering, Nanjing University of Finance and Economics/Collaborative Innovation Center for Modern Grain Circulation and Safety, Nanjing 210023
  • Received:2022-04-26 Accepted:2022-11-25 Online:2023-03-01 Published:2023-03-13

Abstract:

【Background】At present, relevant animal experiments have confirmed that buckwheat had a good intervention effect on obesity and lipid metabolism disorder caused by high-fat diet. At the same time, studies have shown that the adaptive thermogenesis of brown fat could effectively improve the body’s energy metabolism. Therefore, increasing the activity of brown fat and promoting the browning of white fat could be used as an effective way to prevent obesity and improve energy metabolism diseases.【Objective】The raw buckwheat and four kinds of main polyphenols identified from buckwheat were prepared according to the content proportion to study the lipid-lowering effects of buckwheat polyphenols in high-fat diet-induced obese mice via browning of white adipocytes.【Method】Phenolic compounds in buckwheat polyphenol extract were identified by UHPLC-Q-Orbitrap mass spectrometry combined with database. And the main polyphenol compound was prepared according to the content proportion in the raw buckwheat. In order to explore the regulating effects of buckwheat on body weight, organ index and blood lipid level in C57BL/6J mice, the dietary intervention was carried out with 10%, 20% and 40% proportion of buckwheat to replace basic feed and the 2.5 mg∙mL-1 of mixture buckwheat polyphenol standard substance. Last but not least, Western-blot and q-PCR were used to investigate the effects of buckwheat feed and polyphenol intervention on the expression of heat-producing proteins and genes in white and brown fat in mouse subcutaneous adipose tissue.【Result】Twenty phenolic compounds in buckwheat polyphenol extract were identified by UHPLC-Q-Orbitrap mass spectrometry, and the content of four phenolic compounds with the highest content (hydroxycinnamic acid, quercetin,scoparone, and rutin) accounted for more than 80% of the total phenolic compounds, which were the main polyphenols in buckwheat. The results showed that after 39 d in the diet intervention, compared with high-fat diet group, adding buckwheat feed and buckwheat polyphenol intervention on body weight in mice, the liver index and serum triglyceride (TG), total cholesterol (T-CHO), low-density lipoprotein cholesterol (LDL-c), aspartate aminotransferase (ALT) and third transaminase (AST) increased significantly inhibitory effect; with the increase of amount of buckwheat, the inhibition increased. At the same time, adding buckwheat feed and buckwheat polyphenol could protect and improve the decrease of renal index and HDL-c in mice. It was also the high dose 40% buckwheat and polyphenol group that had the best effect, which showed that phenolic substances played a major role in the improvement of abnormal lipid metabolism in high-fat diet-induced obese mice. UCP1, PRDM-16, and PGC-1α protein and gene expression levels were significantly decreased in the high-fat diet group compared with the normal diet group, while Tcf21 and HOXC8 expression levels were significantly increased (P<0.05). After dietary intervention, protein expression levels of UCP1, PRDM-16 and PGC-1α in the buckwheat intervention group were significantly up-regulated, while protein expression levels of Tcf21 and HOXC8 were significantly decreased (P<0.05). In addition, the 40% buckwheat and polyphenol intervention group significantly increased the expression of UCP1, PRDM-16 and PGC-1α genes in mouse visceral adipose tissue (P<0.05), and which down-regulated the expressions of Tcf21 and HOXC8 genes.【Conclusion】Buckwheat intervention could effectively improve the lipid metabolism disorder in high-fat diet-induced obese mice, and it was confirmed that buckwheat polyphenols played a major role. The mechanism was mainly buckwheat polyphenols could significantly improve the thermogenic activity of brown fat, reduce the content of white fat, and regulate the energy metabolism balance. This study provided a new idea and theoretical basis for the utilization of buckwheat and the development of functional foods about lipid-lowering products.

Key words: buckwheat, polyphenols, high-fat diet-induced mice, lipid-lowering effects, browning of white adipocytes

Table 1

Chromatographic gradient elution procedure"

时间Time (min) A (%) B (%)
0 98 2
1 98 2
17 50 50
17.5 50 50
18 98 2
20 98 2

Table 2

Main composition of basic feed"

成分指标 Index of composition 含量 Content (g∙kg-1) 成分指标 Index of composition 含量 Content (g∙kg-1)
水分 Water 100 钙 Calcium 10-18
粗蛋白 Crude protein 180 总磷 Phosphorus 6-12
Oligo T (50 μmol∙L-1) 60 赖氨酸 Lysine 13.2
粗纤维 Coarse fibre 50 蛋氨酸+胱氨酸
Methionine + Cystine
7.8
粗灰分 Coarse ash 80

Table 3

Main ingredients of high-fat diet group and rice bran intervention group feed"

原料
Raw material
对照组
Control group
基础高脂组
High fat group
10%荞麦组
10% Buckwheat group
20%荞麦组
20% Buckwheat group
40%荞麦组
40% Buckwheat group
基础饲料 Basic feed 0.805 0.655 0.555 0.455 0.255
猪油 Lard 0 0.15 0.15 0.15 0.15
蔗糖 Sucrose 0.10 0.10 0.10 0.10 0.10
蛋黄粉 Egg yolk powder 0.08 0.08 0.08 0.08 0.08
胆固醇 Cholesterol 0.01 0.01 0.01 0.01 0.01
胆酸钠 Sodium cholate 0.005 0.005 0.005 0.005 0.005
荞麦 Buckwheat 0 0 0.1 0.2 0.4
合计 Total 1 1 1 1 1

Table 4

Sequences of primers used for real-time qPCR"

基因Genes 上游引物 Upstream primer 下游引物 Downstream primer
PRDM-16 CTGGACCTGAGCATCGGCAG GACGGCCGCAGGTACTTCTC
UCP1 CCCAGAGCCATCTGCATGGG AGGGGACGTCATCTGCCAGT
PGC-1α GAGCACGAGAAGCGGGAGTC CTGTCCGCGTTGTGTCAGGT
Tcf21 AGGAGGAAGGCGCCCACTAA GACGCCAGCCTGAGAGTGTC
HOXC8 CCATGGATGAGACCCCACGC GGGCCCCAGGCAGTTTATCC

Table 5

Composition and identification of polyphenols in buckwheat extract by UHPLC-Q-Orbitrap MS"

保留时间
Retention time
峰面积
Area peak
分子量 Molecular weight 误差值
Error value
分子式
Formula
数据库来源 Annotation source 化合物
Compound
实测值
Measured value
理论值
Theoretical value
mzCloud mzVault ChemSpider
1 1.317 36571473.05 164.158 164.04735 0.11065 C9H8O3 羟基肉桂酸
Hydroxycinnamic acid
2 8.927 6169014.93 302.2357 302.0422 0.1935 C15H10O7 槲皮素 Quercetin
3 11.668 5856748.00 206.195 206.05785 0.13715 C11 H10O4 滨蒿内酯 Scoparone
4 7.446 5688758.95 290.27 290.07866 0.19134 C15H14O6 儿茶素 Epicatechin
5 8.928 3132034.98 610.518 610.15286 0.36514 C27H30O16 芦丁 Rutin
6 12.059 2292049.71 416.3781 416.11025 0.26785 C21H20O9 大豆苷 Daidzin
7 7.403 1199629.88 180.16 180.04219 0.11781 C9H8O4 咖啡酸 Caffeic acid
8 9.284 919736.70 272.25 272.06795 0.18205 C15H12O5 柚皮素 Naringenin
9 11.36 896927.74 178.185 178.06294 0.12206 C10H10O3 甲氧基肉桂酸 Methoxycinnamic acid
10 8.887 776919.85 192.168 192.04226 0.12574 C10H8O4 东莨菪素 Scopoletin
11 12.997 723078.22 576.504 576.12641 0.37759 C30H24O12 原花青素 Procyanidin A2
12 13.099 637134.93 182.17 182.04731 0.12269 C9H10O4 二羟基苯基丙酸Dihydroxyphenylpropionic acid
13 11.237 546215.75 446.41 446.12111 0.28889 C22H22O10 黄豆黄素苷 Glycitin
14 8.929 529856.93 464.3763 464.09526 0.28104 C21H20O12 金丝桃苷 Hyperoside
15 8.052 401414.00 274.27 274.08381 0.18619 C15H14O5 根皮素 Phloretin
16 6.109 369541.11 452.41 452.13163 0.27837 C21H24O11 虾青素 Aspalathin
17 8.323 249449.72 610.55 610.18694 0.36306 C28H34O15 橙皮甙 Hesperidin
18 7.458 237259.65 290.28 290.06056 0.21944 C15H14O6 儿茶酸 Catechin
19 8.3 91517.24 448.3769 448.09996 0.27694 C21H20O11 槲皮甙 Quercitrin
20 9.492 52981.16 316.262 316.05763 0.20437 C16H12O7 异鼠李素 Isorhamnetin

Fig. 1

Effects of different content of buckwheat and polyphenol mixture supplementation on the body weight of high-fat diet- induced mice The same as below"

Fig. 2

Effects of different content of buckwheat and polyphenol mixture supplementation on the liver (A), kidney (B), heart (C), pancreas organ (D) index of high-fat diet-induced mice The same as below"

Fig. 3

Effects of different content of buckwheat and polyphenol mixture supplementation on the T-CHO (A), TG (B), LDL-c (C), HDL-c (D), ALT (E), AST (F) of high-fat diet-induced mice The same as below"

Fig. 4

Histological analysis for liver of mice Con: Basic diet group; HFD: High-fat diet group; HPE: High-fat diet group was given polyphenols; 10%: Feed containing 10% buckwheat; 20%: Feed containing 20% buckwheat; 40%: Feed containing 40% buckwheat"

Fig. 5

Effects of different content of buckwheat and polyphenol mixture supplementation on the expression levels of thermogenesis- related proteins in subcutaneous adipose tissues"

Fig. 6

Effect of different content of buckwheat and polyphenol mixture supplementation on the expression levels of thermogenesis-related genes in subcutaneous adipose tissues"

[1]
BRAY G A, FRÜHBECK G, RYAN D H, WILDING J P. Management of obesity. The Lancet, 2016, 387(10031): 1947-1956.

doi: 10.1016/S0140-6736(16)00271-3
[2]
SCULLY T. Public health: Society at large. Nature, 2014, 508(7496): S50-S51.

doi: 10.1038/508S50a
[3]
RUBY M A, MASSART J, HUNERDOSSE D M, SCHÖNKE M, CORREIA J C, LOUIE S M, ZIERATH J R. Human carboxylesterase 2 reverses obesity-induced diacylglycerol accumulation and glucose intolerance. Cell Reports, 2017, 18(3): 636-646.

doi: S2211-1247(16)31777-6 pmid: 28099843
[4]
CHEN G J, XIE M H, DAI Z Q, WAN P, YE H, ZENG X X, SUN Y. Kudingcha and fuzhuan brick tea prevent obesity and modulate gut microbiota in high-fat diet fed mice. Molecular Nutrition & Food Research, 2018, 62(6): 1700485.
[5]
LU P, ZHANG F C, QIAN S W, LI X, CUI Z, DANG Y J, TANG Q Q. Artemisinin derivatives prevent obesity by inducing browning of WAT and enhancing BAT function. Cell Research, 2016, 26(10): 1169.

doi: 10.1038/cr.2016.108 pmid: 27633061
[6]
LIU L, WEN W, ZHANG R F, WEI Z C, DENG Y Y, XIAO J, ZHANG M W. Complex enzyme hydrolysis releases antioxidative phenolics from rice bran. Food Chemistry, 2017, 214: 1-8.

doi: S0308-8146(16)31060-3 pmid: 27507440
[7]
ZHAI X C, LIN D H, ZHAO Y, LI W W, YANG X B. Enhanced anti-obesity effects of bacterial cellulose combined with konjac glucomannan in high-fat diet-fed C57BL/6J mice. Food & Function, 2018, 9(10): 5260-5272.
[8]
LIU W, ZHAO S Q, WANG J Q, SHI J, SUN Y K, WANG W Q, NING G, HONG J, LIU R X. Grape seed proanthocyanidin extract ameliorates inflammation and adiposity by modulating gut microbiota in high-fat diet mice. Molecular Nutrition & Food Research, 2017, 61(9): 1601082.
[9]
谢佳函, 刘回民, 刘美宏, 郑明珠, 徐倩, 刘景圣. 杂粮多酚功能活性研究进展. 食品工业科技, 2017, 38(14): 326-329, 335.
XIE J H, LIU H M, LIU M H, ZHENG M Z, XU Q, LIU J S. Research progress of functional activities of polyphenols in coarse cereals. Science and Technology of Food Industry, 2017, 38(14): 326-329, 335.(in Chinese)
[10]
HUANG D W, CHUNG C P, KUO Y H, LIN Y L, CHIANG W C. Identification of compounds in adlay (Coix lachryma-jobi L. var. ma-yuen Stapf) seed hull extracts that inhibit lipopolysaccharide- induced inflammation in RAW 264.7 Macrophages. Journal of Agricultural & Food Chemistry, 2009, 57(22): 10651-10657.
[11]
肖杰, 王曦, 侯粲, 牛兴和, 董志忠, 应剑. 苦荞调控糖脂代谢作用及其生物学机制研究进展. 食品科学, 2019, 40(21): 343-349.
XIAO J, WANG X, HOU C, NIU X H, DONG Z Z, YING J. Recent advances in understanding the role and mechanism of action of Tartary buckwheat in regulating glucolipid metabolism. Food Science, 2019, 40(21): 343-349.(in Chinese)
[12]
SONG Z, REVELO X, SHAO W, TIAN L, ZENG K, LEI H, SUN H S, MINNA W, DANIEL W, JIN T. Dietary curcumin intervention targets mouse white adipose tissue inflammation and brown adipose tissue UCP1 expression: Curcumin intervention targets both WAT and BAT. Obesity, 2018, 26(3): 547558.
[13]
YOU Y L, YUAN X X, LIU X M, LIANG C, MENG M H, HUANG Y Y, HAN X, GUO J L, GUO Y, REN C L, ZHANG Q W, SUN X Y, MA T T, LIU G J, JIN W Z, HUANG W D, ZHAN J C. Cyanidin-3-glucoside increases whole body energy metabolism by upregulating brown adipose tissue mitochondrial function. Molecular Nutrition & Food Research, 2017, 61(11): 1700261.
[14]
LAGOUGE M, ARGMANN C, GERHART-HINES Z, MEZIANE H, LERIN C, DAUSSIN F, AUWERX J. Resveratrol improves mitochondrial function and protects against metabolic disease by activating SIRT1 and PGC-1alpha. Cell, 2006, 127(6): 1109-1122.

doi: 10.1016/j.cell.2006.11.013 pmid: 17112576
[15]
SEALE P, BJORK B, YANG W L, KAJIMURA S, CHIN S, KUANG S H, SCIME A, DEVARAKONDA S, CONROE H M, ERDJUMENT- BROMAGE H. PRDM16 controls a brown fat/skeletal muscle switch. Nature, 2008, 454(7207): 961-967.

doi: 10.1038/nature07182
[16]
WALDÉN T B, HANSEN I R, TIMMONS J A, CANNON B, NEDERGAARD J. Recruited vs. nonrecruited molecular signatures of brown, “brite,” and white adipose tissues. American Journal of Physiology Endocrinology & Metabolism, 2012, 302(1): E19-E31.
[17]
YAO Y L, XU F R, JU X R, LI Z F, WANG L F. Lipid-lowering effects and intestinal transport of polyphenol extract from digested buckwheat in Caco-2/HepG2 coculture models. Journal of Agricultural and Food Chemistry, 2020, 68(14): 4205-4214.

doi: 10.1021/acs.jafc.0c00321 pmid: 32141744
[18]
WATERMAN C, ROJAS-SILVA P, TUMER T B, KUHN P, RICHARD A J, WICKS S, STEPHENS J M, WANG Z, MYNATT R, CEFALU W, RASKIN I. Isothiocyanate-rich Moringa oleifera extract reduces weight gain, insulin resistance, and hepatic gluconeogenesis in mice. Molecular Nutrition & Food Research, 2015, 59(6): 1013-1024.
[19]
WANG J Q, LIU R X, WANG F, HONG J, LI X Y, CHEN M P, YE Y Y, ZHANG X F, MA Q Y, WANG R, SHI J, CUI B, GU W Q, ZHANG Y F, ZHANG Z G, WANG W Q, XIA X F, LIU M Y, NING G. Ablation of LGR4 promotes energy expenditure by driving white-to-brown fat switch. Nature Cell Biology, 2013, 15(12): 1455-1463.

doi: 10.1038/ncb2867 pmid: 24212090
[20]
BUETTNER R, SCHÖLMERICH J, BOLLHEIMER L C. High-fat diets: Modeling the metabolic disorders of human obesity in rodents. Obesity, 2007, 15(4): 798-808.

doi: 10.1038/oby.2007.608 pmid: 17426312
[21]
SINGH B N, SHANKAR S, SRIVASTAVA R K. Green tea catechin, epigallocatechin-3-gallate (EGCG): Mechanisms, perspectives and clinical applications. Biochemical Pharmacology, 2011, 82(12): 1807-1821.

doi: 10.1016/j.bcp.2011.07.093 pmid: 21827739
[22]
MURPHY E F, COTTER P D, HOGAN A, OSULLIVAN O, JOYCE A, FOUHY F, SHANAHAN F. Divergent metabolic outcomes arising from targeted manipulation of the gut microbiota in diet-induced obesity. Gut Microbes, 2013, 62(1): 220-226.
[23]
LOOMBA R, SANYAL A J. The global NAFLD epidemic. Nature Reviews Gastroenterology & Hepatology, 2013, 10(11): 686-690.
[24]
FENG X J, YU W, LI X D, ZHOU F F, ZHANG W L, SHEN Q, LI J X, ZHANG C, SHEN P P. Apigenin, a modulator of PPARγ, attenuates HFD-induced NAFLD by regulating hepatocyte lipid metabolism and oxidative stress via Nrf2 activation. Biochemical Pharmacology, 2017, 136: 136-149.

doi: S0006-2952(17)30231-9 pmid: 28414138
[25]
QU L L, LIU Q Q, ZHANG Q, TUO X X, FAN D D, DENG J J, YANG H X. Kiwifruit seed oil prevents obesity by regulating inflammation, thermogenesis, and gut microbiota in high-fat diet- induced obese C57BL/6 mice. Food and Chemical Toxicology, 2019, 125: 85-94.

doi: 10.1016/j.fct.2018.12.046
[26]
SUDIRMAN S, CHANG H W, CHEN C K, KONG Z L. A dietary polysaccharide from Eucheuma cottonii downregulates proinflammatory cytokines and ameliorates osteoarthritis-associated cartilage degradation in obese rats. Food & Function, 2019, 10(9): 5697-5706.
[27]
WANG J J, TANG H, ZHANG C H, ZHAO Y F, DERRIEN M, ROCHER E, VAN-HYLCKAMA VLIEG J E T, STRISSEL K, ZHAO L P, OBIN M, SHEN J. Modulation of gut microbiota during probiotic-mediated attenuation of metabolic syndrome in high fat diet-fed mice. The ISME Journal, 2015, 9: 1-15.

doi: 10.1038/ismej.2014.99
[28]
PORTER C, HERNDON D N, CHONDRONIKOLA M, CHAO T, ANNAMALAI P, BHATTARAI N, SARAF M K, CAPEK K D, REIDY P, DAQUIANG A C, KOLONIN M G, RASMUSSEN B B, BORSHEIM E, KINSKY T T, SIDOSSIS L S. Human and mouse brown adipose tissue mitochondria have comparable UCP1 function. Cell Metabolism, 2016, 24(2): 246-255.

doi: 10.1016/j.cmet.2016.07.004 pmid: 27508873
[1] ZHAO HaiXia,XIAO Xin,DONG QiXin,WU HuaLa,LI ChengLei,WU Qi. Optimization of Callus Genetic Transformation System and Its Application in FtCHS1 Overexpression in Tartary Buckwheat [J]. Scientia Agricultura Sinica, 2022, 55(9): 1723-1734.
[2] ZHENG FengSheng,WANG HaiHua,WU QingTao,SHEN Quan,TIAN JianHong,PENG XiXu,TANG XinKe. Genome-Wide Identification of VQ Gene Family in Fagopyrum tataricum and Its Expression Profiles in Response to Leaf Spot Pathogens [J]. Scientia Agricultura Sinica, 2021, 54(19): 4048-4060.
[3] HOU SiYu,WANG XinFang,DU Wei,FENG JinHua,HAN YuanHuai,LI HongYing,LIU LongLong,SUN ZhaoXia. Genome-Wide Identification of WOX Family and Expression Analysis of Callus Induction Rate in Tartary Buckwheat [J]. Scientia Agricultura Sinica, 2021, 54(17): 3573-3586.
[4] HAO YanRong,DU Wei,HOU SiYu,WANG DongHang,FENG HongMei,HAN YuanHuai,ZHOU MeiLiang,ZHANG KaiXuan,LIU LongLong,WANG JunZhen,LI HongYing,SUN ZhaoXia. Identification of ARF Gene Family and Expression Pattern Induced by Auxin in Fagopyrum tataricum [J]. Scientia Agricultura Sinica, 2020, 53(23): 4738-4749.
[5] WU CaoYang,LIANG ShiHan,QIU Jun,GAO JinFeng,GAO XiaoLi,WANG PengKe,FENG BaiLi,YANG Pu. An Examination on Breeding Status Quo of Chinese Tartary Buckwheat Varieties Based on the National Cross-Country Tests of Tartary Buckwheat Varieties in China over 12 Consecutive Years [J]. Scientia Agricultura Sinica, 2020, 53(19): 3878-3892.
[6] SHE HengZhi, NIE Jiao, LI YingShuang, ZHANG YuKe, HUANG KeHui, ZHANG YuanLi, FANG XiaoMei, RUAN RenWu, YI ZeLin. Effects of Silicon Application Rate on Common Buckwheat Lodging and Yield [J]. Scientia Agricultura Sinica, 2018, 51(14): 2664-2674.
[7] LIANG Di, YANG Xi, GUO YuRong. Effects of Different Concentrations of Apple Polyphenols on the Physicochemical Properties of Chitosan Membrane Fluids [J]. Scientia Agricultura Sinica, 2018, 51(14): 2799-2813.
[8] CHANG XueLing, ZHANG ZongWen, LI YanQin, GAO Jia. Cloning and Expression Analyses of the mate Gene in Buckwheat [J]. Scientia Agricultura Sinica, 2018, 51(11): 2038-2048.
[9] SHE HengZhi, NIE Jiao, LI YingShuang, LIU XingBei, HU Dan, MA Shan, Ciren zhuoga, WANG Can, WU DongQian, RUAN RenWu, YI ZeLin. Lignin and Lignin Monomer Synthetic Characteristics of Culm in Common Buckwheat with Different Lodging Resistance Capabilities [J]. Scientia Agricultura Sinica, 2017, 50(7): 1202-1209.
[10] DONG Li-hong, ZHANG Rui-fen, XIAO Juan, DENG Yuan-yuan, ZHANG Yan, LIU Lei, HUANG Fei, WEI Zhen-cheng, ZHANG Ming-wei. Separation and Antioxidant Activity of Different Phenolic Compound Fractions from Litchi Pulp [J]. Scientia Agricultura Sinica, 2016, 49(20): 4004-4015.
[11] QU Yang, ZHOU Yu, WANG Zhao, WANG Peng-ke, GAO Jin-feng, GAO Xiao-li, FENG Bai-li . Analysis of Genetic Diversity and Structure of Tartary Buckwheat Resources from Production Regions [J]. Scientia Agricultura Sinica, 2016, 49(11): 2049-2062.
[12] HU Dan, LIU Xing-bei, WANG Can, YANG Hao, LI He-xin, RUAN Ren-wu, YUAN Xiao-hui, YI Ze-lin. Expression Analysis of Key Enzyme Genes in Lignin Synthesis of Culm Among Different Lodging Resistances of Common Buckwheat (Fagopyrum esculentum Moench) [J]. Scientia Agricultura Sinica, 2015, 48(9): 1864-1872.
[13] LI Hong, DONG Shuo, XIONG Ying, GU Ming-can, GUO Kai-jun. Effect of Chestnut Involucres Polyphenols on Growth Performance and Antioxidant Properties of AA Broilers [J]. Scientia Agricultura Sinica, 2015, 48(4): 788-795.
[14] LIU Xing-bei, WU Dong-qian, WANG Can, HU Dan, YANG Hao, SHE Heng-zhi, RUAN Ren-wu,YUAN Xiao-hui, YI Ze-lin. Effects of Spraying Uniconazole on Lodging Resistance of Culm and Yield in Common Buckwheat [J]. Scientia Agricultura Sinica, 2015, 48(24): 4903-4915.
[15] YAN Ya-mei, DAI Guo-li, RAN Lin-wu, LUO Qing, LI Xiao-ying, QIN Ken, WU Peng-ju, ZENG Xiao-xiong, CAO You-long. The Polyphenols Composition of Lycium ruthenicum Murr. from Different Places [J]. Scientia Agricultura Sinica, 2014, 47(22): 4540-4550.
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed   
No Suggested Reading articles found!