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[PMID]: 29325003
[Au] Autor:Song B; Stöcklin J; Armbruster WS; Gao Y; Peng D; Sun H
[Ad] Address:Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Sciences, Yunnan, China.
[Ti] Title:Reversible colour change in leaves enhances pollinator attraction and reproductive success in Saururus chinensis (Saururaceae).
[So] Source:Ann Bot;, 2018 Jan 09.
[Is] ISSN:1095-8290
[Cp] Country of publication:England
[La] Language:eng
[Ab] Abstract:Background and Aims: Although there has been much experimental work on leaf colour change associated with selection generated by abiotic environmental factors and antagonists, the role of leaf colour change in pollinator attraction has been largely ignored. We tested whether whitening of the apical leaves subtending the inflorescences of Saururus chinensis during flowering enhances pollinator attraction, and whether re-greening of the white leaves after flowering increases carbon assimilation and promotes seed development. Methods: White leaves were removed or covered, and the effects of these manipulations on pollinator visitation and subsequent reproductive success were assessed. The net photosynthetic rates of leaves of different colour were measured and their photosynthetic contributions to seed development were evaluated. Key Results: Saururus chinensis is able to self-pollinate autonomously, but depends largely on flies for pollination. White leaves had different reflectance spectra from green leaves, and white leaves attracted significantly more pollinators and led to significantly higher fruit and seed set. Although leaf whitening resulted in a reduction in photosynthetic capacity, it translated into only a small decrease in seed mass. When leaves had turned back from white to green after flowering their photosynthetic capacity was similar to that of 'normal' green leaves and promoted seed development. Conclusions: The reversible leaf colour change in S. chinensis appears to be adaptive because it enhances pollination success during flowering, with a small photosynthetic cost, while re-greening of these leaves after flowering helps to meet the carbon requirements for seed development.
[Pt] Publication type:JOURNAL ARTICLE
[Em] Entry month:1801
[Cu] Class update date: 180308
[Lr] Last revision date:180308
[St] Status:Publisher
[do] DOI:10.1093/aob/mcx195

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[PMID]: 29498658
[Au] Autor:Gong EC; Chea S; Balupuri A; Kang NS; Chin YW; Choi YH
[Ad] Address:College of Pharmacy and Intergrated Research Institute for Drug Development, Dongguk University-Seoul, 32 Dongguk-lo, Ilsandong-gu, Goyang, Gyeonggi-do 10326, Korea. dmsco3901@hanmail.net.
[Ti] Title:Enzyme Kinetics and Molecular Docking Studies on Cytochrome 2B6, 2C19, 2E1, and 3A4 Activities by Sauchinone.
[So] Source:Molecules;23(3), 2018 Mar 02.
[Is] ISSN:1420-3049
[Cp] Country of publication:Switzerland
[La] Language:eng
[Ab] Abstract:Sauchinone, an active lignan isolated from the aerial parts of (Saururaceae), exhibits anti-inflammatory, anti-obesity, anti-hyperglycemic, and anti-hepatic steatosis effects. As herb-drug interaction (HDI) through cytochrome P450s (CYPs)-mediated metabolism limits clinical application of herbs and drugs in combination, this study sought to explore the enzyme kinetics of sauchinone towards CYP inhibition in in vitro human liver microsomes (HLMs) and in vivo mice studies and computational molecular docking analysis. In in vitro HLMs, sauchinone reversibly inhibited CYP2B6, 2C19, 2E1, and 3A4 activities in non-competitive modes, showing inhibition constant ) values of 14.3, 16.8, 41.7, and 6.84 µM, respectively. Also, sauchinone time-dependently inhibited CYP2B6, 2E1 and 3A4 activities in vitro HLMs. Molecular docking study showed that sauchinone could be bound to a few key amino acid residues in the active site of CYP2B6, 2C19, 2E1, and 3A4. When sibutramine, clopidogrel, or chlorzoxazone was co-administered with sauchinone to mice, the systemic exposure of each drug was increased compared to that without sauchinone, because sauchinone reduced the metabolic clearance of each drug. In conclusion, when sauchinone was co-treated with drugs metabolized via CYP2B6, 2C19, 2E1, or 3A4, sauchinone-drug interactions occurred because sauchinone inhibited the CYP-mediated metabolic activities.
[Pt] Publication type:JOURNAL ARTICLE
[Em] Entry month:1803
[Cu] Class update date: 180302
[Lr] Last revision date:180302
[St] Status:In-Process

  3 / 174 MEDLINE  
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[PMID]: 28701654
[Au] Autor:Asakawa Y; Tomiyama K; Sakurai K; Kawakami Y; Yaguchi Y
[Ad] Address:Faculty of Pharmaceutical Sciences, Tokushima Bunri University.
[Ti] Title:Volatile Compounds from the Different Organs of Houttuynia cordata and Litsea cubeba (L. citriodora).
[So] Source:J Oleo Sci;66(8):889-895, 2017 Aug 01.
[Is] ISSN:1347-3352
[Cp] Country of publication:Japan
[La] Language:eng
[Ab] Abstract:The volatile compounds obtained from the different organs of Houttuynia cordata (Saururaceae) and Litsea cubeba (Lauraceae) were analyzed by Gas Chromatography/Mass Spectrometry (GC/MS), Headspace Solid Phase Micro Extraction-Gas Chromatography/Mass Spectrometry (HS-SPME-GC/MS), and GC/olfactometry (GC/O). The major component of all parts of H. cordata is assigned as 4-tridecanone. Each organ produces myrcene as the major monoterpenoid. The major monoterpene in the rhizomes and roots was ß-pinene instead of myrcene. 1-Decanal which was responsible for the unpleasant odor of this plant, was the predominant polyketide in both leaves and stems. The presence of 1-decanal was very poor in flowers, stem collected in summer, rhizomes, and roots. GC/MS analyses were very simple in case of the crude extracts of flowers. The content of sesquiterpenoids was extremely poor. (8Z)-Heptadecene, geranial, and neral were detected as the major components in Litsea cubeba. Odor-contributing components by GC/O analysis of the ether extract of the fresh flowers of L. cubeba were neral and geranial which played an important role in sweet-lemon fragrance of the flowers. The role of a high content of (8Z)-heptadecene was still unknown but it might play a significant role in the dispersion of the volatile monoterpene hydrocarbons and aldehydes. The flower volatiles of the Japanese L. cubeba were chemically quite different from those of the Chinese same species.
[Mh] MeSH terms primary: Houttuynia/chemistry
Litsea/chemistry
Plant Structures
Volatile Organic Compounds/analysis
[Mh] MeSH terms secundary: Alkanes/analysis
Alkenes/analysis
Bridged Bicyclo Compounds/analysis
Fatty Alcohols/analysis
Gas Chromatography-Mass Spectrometry/methods
Litsea/anatomy & histology
Monoterpenes/analysis
Olfactometry
Polyketides/analysis
Sesquiterpenes/analysis
[Pt] Publication type:JOURNAL ARTICLE
[Nm] Name of substance:0 (Alkanes); 0 (Alkenes); 0 (Bridged Bicyclo Compounds); 0 (Fatty Alcohols); 0 (Monoterpenes); 0 (Polyketides); 0 (Sesquiterpenes); 0 (Volatile Organic Compounds); 3M39CZS25B (myrcene); 4MS8VHZ1HJ (beta-pinene); 89V4LX791F (n-decyl alcohol); A3LZF0L939 (tridecane); H7C0J39XUM (heptadecane); T7EU0O9VPP (citral)
[Em] Entry month:1710
[Cu] Class update date: 171010
[Lr] Last revision date:171010
[Js] Journal subset:IM
[Da] Date of entry for processing:170714
[St] Status:MEDLINE
[do] DOI:10.5650/jos.ess17049

  4 / 174 MEDLINE  
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[PMID]: 28636756
[Au] Autor:Verma RS; Joshi N; Padalia RC; Singh VR; Goswami P; Kumar A; Iqbal H; Verma RK; Chanda D; Chauhan A; Saikia D
[Ad] Address:CSIR-Central Institute of Medicinal and Aromatic Plants, Research Centre, Pantnagar, Uttarakhand, India.
[Ti] Title:Chemical Composition and Allelopathic, Antibacterial, Antifungal, and Antiacetylcholinesterase Activity of Fish-mint (Houttuynia cordataThunb.) from India.
[So] Source:Chem Biodivers;14(10), 2017 Oct.
[Is] ISSN:1612-1880
[Cp] Country of publication:Switzerland
[La] Language:eng
[Ab] Abstract:Fish-mint (Houttuynia cordataThunb.), belonging to family Saururaceae, has long been used as food and traditional herbal medicine. The present study was framed to assess the changes occurring in the essential-oil composition of H. cordata during annual growth and to evaluate allelopathic, antibacterial, antifungal, and antiacetylcholinesterase activities. The essential-oil content ranged from 0.06 - 0.14% and 0.08 - 0.16% in aerial parts and underground stem, respectively. The essential oils were analysed by GC-FID, GC/MS, and NMR ( H and C). Major constituents of aerial-parts oil was 2-undecanone (19.4 - 56.3%), myrcene (2.6 - 44.3%), ethyl decanoate (0.0 - 10.6%), ethyl dodecanoate (1.1 - 8.6%), 2-tridecanone (0.5 - 8.3%), and decanal (1.1 - 6.9%). However, major constituents of underground-stem oil were 2-undecanone (29.5 - 42.3%), myrcene (14.4 - 20.8%), sabinene (6.0 - 11.1%), 2-tridecanone (1.8 - 10.5%), ß-pinene (5.3 - 10.0%), and ethyl dodecanoate (0.8 - 7.3%). Cluster analysis revealed that essential-oil composition varied substantially due to the plant parts and season of collection. The oils exhibited significant allelopathic (inhibition: 77.8 - 88.8%; LD : 2.45 - 3.05 µl/plate), antibacterial (MIC: 0.52 - 2.08 µl/ml; MBC: bacteriostatic) and antifungal (MIC: 2.08 - 33.33 µl/ml; MFC: 4.16 - 33.33 µl/ml) activities. The results indicate that the essential oil from H. cordata has a significant potential to allow future exploration and exploitation as a natural antimicrobial and allelopathic agent.
[Pt] Publication type:JOURNAL ARTICLE
[Em] Entry month:1706
[Cu] Class update date: 171018
[Lr] Last revision date:171018
[St] Status:In-Process
[do] DOI:10.1002/cbdv.201700189

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[PMID]: 28626610
[Au] Autor:Grímsson F; Grimm GW; Zetter R
[Ad] Address:Department of Palaeontology, University of Vienna, Vienna, Austria.
[Ti] Title:Tiny pollen grains: first evidence of Saururaceae from the Late Cretaceous of western North America.
[So] Source:PeerJ;5:e3434, 2017.
[Is] ISSN:2167-8359
[Cp] Country of publication:United States
[La] Language:eng
[Ab] Abstract:BACKGROUND: The Saururaceae, a very small family of Piperales comprising only six species in four genera, have a relatively scanty fossil record outside of Europe. The phylogenetic relationships of the four genera to each other are resolved, with the type genus occurring in both eastern North America and East Asia. No extant species occurs in western Eurasia. The most exceptional find so far has been an inflorescence with pollen, S.Y.Sm. & Stockey from Eocene of North America with strong affinities to extant species of Recent dated trees suggest, however, an Eocene or younger crown age for the family. METHODS: Dispersed fossil pollen grains from the Campanian (82-81 Ma) of North America are compared to dispersed pollen grains from the Eocene strata containing the Miocene of Europe, and extant members of the family using combined LM and SEM imaging. RESULTS: The unambiguous fossil record of the Saururaceae is pushed back into the Campanian (82-81 Ma). Comparison with re-investigated pollen from the Eocene of North America, the Miocene of Europe, and modern species of the family shows that pollen morphology in Saururaceae is highly conservative, and remained largely unchanged for the last 80 million years. DISCUSSION: Campanian pollen of Saururaceae precludes young (Eocene or younger) estimates for the Saururaceae root and crown age, but is in-line with maximum age scenarios. type pollen appear to represent the primitive pollen morphology of the family. Often overlooked because of its small size, dispersed Saururaceae pollen may provide a unique opportunity to map the geographic history of a small but old group of Piperales, and should be searched for in Paleogene and Cretaceous sediment samples.
[Pt] Publication type:JOURNAL ARTICLE
[Em] Entry month:1706
[Cu] Class update date: 170816
[Lr] Last revision date:170816
[St] Status:PubMed-not-MEDLINE
[do] DOI:10.7717/peerj.3434

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[PMID]: 28278686
[Au] Autor:Li C; Li N; Yue J; Song Q; Fan Q
[Ad] Address:a Key Laboratory of Tropical Plant Resources and Sustainable Use, Xishuangbanna Tropical Botanical Garden , Chinese Academy of Sciences , Kunming , P.R. China.
[Ti] Title:Two new lignans from Saururus chinensis.
[So] Source:Nat Prod Res;31(14):1598-1603, 2017 Jul.
[Is] ISSN:1478-6427
[Cp] Country of publication:England
[La] Language:eng
[Ab] Abstract:Two new lignans, (Z)-14-bis(3',4'-dimethoxyphenyl)-2,3-dimethylbut-2-ene-1,4-dione (1), threo-2-methyl-3-oxo-1-(3',4',5'-trimethoxyphenyl)butyl-3″,4″-dimethoxybenzoate (2), together with 15 known derivatives (3-17) were isolated from Saururus chinensis. Their structures were determined on the basis of spectral data, including 1D and 2D NMR experiments and HREIMS spectra. The antitumour activity was screened by MTT assay, compounds 1, 2, 3, 5, 9-11 and 13-15 showed no cytotoxic activity against HL-60, SMMC-7721, A549, MCF-7 and SW480 cell lines.
[Mh] MeSH terms primary: Lignans/isolation & purification
Saururaceae/chemistry
[Mh] MeSH terms secundary: Cell Line, Tumor
Humans
Lignans/chemistry
Molecular Structure
Plant Extracts/chemistry
Plant Roots/chemistry
Spectrum Analysis
[Pt] Publication type:JOURNAL ARTICLE
[Nm] Name of substance:0 (Lignans); 0 (Plant Extracts)
[Em] Entry month:1709
[Cu] Class update date: 170922
[Lr] Last revision date:170922
[Js] Journal subset:IM
[Da] Date of entry for processing:170311
[St] Status:MEDLINE
[do] DOI:10.1080/14786419.2017.1286483

  7 / 174 MEDLINE  
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[PMID]: 27908800
[Au] Autor:Gao X; He J; Wu XD; Peng LY; Shao LD; Li Y; Cheng X; Zhao QS
[Ad] Address:College of Biological Resources and Food Engineering, Qujing Normal University, Qujing 655011, People's Republic of China.
[Ti] Title:Sauruchinenols A and B, unprecedented monocyclic diterpenes with new carbon skeleton from the aerial parts of Saururus chinensis.
[So] Source:Fitoterapia;116:116-120, 2017 Jan.
[Is] ISSN:1873-6971
[Cp] Country of publication:Netherlands
[La] Language:eng
[Ab] Abstract:Sauruchinenols A (1) and B (2), two novel monocyclic diterpenes with unique carbon skeleton, as well as two new structurally related diterpenes, sauruchinenols C (3) and D (4), were isolated from the aerial part of Saururus chinensis. Their structures were elucidated based on the analysis of spectroscopic data. A hypothetical biogenetic pathway for sauruchinenols A and B was proposed.
[Mh] MeSH terms primary: Diterpenes/chemistry
Plant Components, Aerial/chemistry
Saururaceae/chemistry
[Mh] MeSH terms secundary: Animals
Diterpenes/isolation & purification
Mice
Molecular Structure
Nitric Oxide/metabolism
RAW 264.7 Cells
[Pt] Publication type:JOURNAL ARTICLE
[Nm] Name of substance:0 (Diterpenes); 0 (sauruchinenol A); 0 (sauruchinenol B); 31C4KY9ESH (Nitric Oxide)
[Em] Entry month:1701
[Cu] Class update date: 170118
[Lr] Last revision date:170118
[Js] Journal subset:IM
[Da] Date of entry for processing:161203
[St] Status:MEDLINE

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[PMID]: 27618865
[Au] Autor:Lee JH; Lee JJ; Cho WK; Yim NH; Kim HK; Yun B; Ma JY
[Ad] Address:Korean Medicine (KM) Application Center, Korea Institute of Oriental Medicine, Daegu, 700-300, Republic of Korea.
[Ti] Title:KBH-1, an herbal composition, improves hepatic steatosis and leptin resistance in high-fat diet-induced obese rats.
[So] Source:BMC Complement Altern Med;16:355, 2016 Sep 13.
[Is] ISSN:1472-6882
[Cp] Country of publication:England
[La] Language:eng
[Ab] Abstract:BACKGROUND: KBH-1 is an herbal mixture of Saururus chinensis, Curcuma longa and Polygala tenuifolia. Each herb has been reported to have various pharmaceutical activities; however, the synergistic effect of this herbal composition on obesity has not yet been determined. We investigated the alleviation effect of KBH-1 and its possible molecular mechanism in obesity-induced hepatic steatosis and leptin resistance in the hypothalamus. METHODS: We used HepG2 cells, primary neuronal cells and a high-fat diet (HFD)-induced obesity rat model to determine the effect of KBH-1 in vitro and in vivo on hepatic steatosis and leptin resistance accompanied by obesity. To identify the alleviation effect on lipid accumulation, HepG2 cells stimulated by FFA were stained with Oil Red O; in addition, immunoblotting and qPCR were performed to determine the effect of KBH-1 on the activation of proteins and nuclear enzymes in HepG2 cells and the steatotic liver of HFD-induced obesity rats. To examine the effect of KBH-1 on the leptin resistance of the hypothalamus and its possible molecular mechanism, we examined the effect of KBH-1 on the activation of the leptin resistance-related protein in primary cultured cortical neuron cells and the hypothalamus of an HFD-induced obesity rat model. In addition, we used HPLC analysis to identify the standard compound of KBH-1. RESULTS: KBH-1 not only suppressed the lipid deposition in HepG2 cells exposed to free fatty acids (FFA) but also significantly down-regulated major factors in lipogenesis and up-regulated major factors in lipolysis. Similarly, in a HFD-induced obesity model, KBH-1 improved hepatic steatosis by alleviating the effects on lipogenic genes and kinases. In addition, KBH-1 significantly improved the leptin-mediated signals impaired by obesity or FFA in the obesity model and primary cultured cortical neuron cells. In addition, KBH-1 was analyzed to include six standard compounds using HPLC analysis, among these compounds, onji-saponin B and curcumin were potently suppressed the level of triglycerides. CONCLUSIONS: KBH-1 exhibits alleviating effects by improving hepatic steatosis and leptin resistance by up-regulating the activation of AMPK and suppressing the expression of PPARγ. These findings show the potential of KBH-1 as a functional food supplement or preventive agent in the treatment of obesity.
[Mh] MeSH terms primary: Drugs, Chinese Herbal/pharmacology
Drugs, Chinese Herbal/therapeutic use
Fatty Liver/drug therapy
Fatty Liver/metabolism
Insulin Resistance
Leptin/metabolism
[Mh] MeSH terms secundary: Animals
Curcuma/chemistry
Diet, High-Fat
Hep G2 Cells
Humans
Male
Polygala/chemistry
Rats
Rats, Sprague-Dawley
Saururaceae/chemistry
[Pt] Publication type:JOURNAL ARTICLE
[Nm] Name of substance:0 (Drugs, Chinese Herbal); 0 (Leptin)
[Em] Entry month:1702
[Cu] Class update date: 170222
[Lr] Last revision date:170222
[Js] Journal subset:IM
[Da] Date of entry for processing:160914
[St] Status:MEDLINE
[do] DOI:10.1186/s12906-016-1265-z

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[PMID]: 27413739
[Au] Autor:Sekita Y; Murakami K; Yumoto H; Amoh T; Fujiwara N; Ogata S; Matsuo T; Miyake Y; Kashiwada Y
[Ad] Address:Department of Pharmacognosy, Institute of Biomedical Sciences, Tokushima University Graduate School, 1-78-1 Shou-machi, Tokushima 770-8505, Japan.
[Ti] Title:Preventive Effects of Houttuynia cordata Extract for Oral Infectious Diseases.
[So] Source:Biomed Res Int;2016:2581876, 2016.
[Is] ISSN:2314-6141
[Cp] Country of publication:United States
[La] Language:eng
[Ab] Abstract:Houttuynia cordata (HC) (Saururaceae) has been used internally and externally as a traditional medicine and as an herbal tea for healthcare in Japan. Our recent survey showed that HC poultice (HCP) prepared from smothering fresh leaves of HC had been frequently used for the treatment of purulent skin diseases with high effectiveness. Our experimental study also demonstrated that ethanol extract of HCP (eHCP) has antibacterial, antibiofilm, and anti-inflammatory effects against S. aureus which caused purulent skin diseases. In this study, we focused on novel effects of HCP against oral infectious diseases, such as periodontal disease and dental caries. We determined the antimicrobial and antibiofilm effects of water solution of HCP ethanol extract (wHCP) against important oral pathogens and investigated its cytotoxicity and anti-inflammatory effects on human oral epithelial cells. wHCP had moderate antimicrobial effects against some oral microorganisms and profound antibiofilm effects against Fusobacterium nucleatum, Streptococcus mutans, and Candida albicans. In addition, wHCP had no cytotoxic effects and could inhibit interleukin-8 and CCL20 productions by Porphyromonas gingivalis lipopolysaccharide-stimulated human oral keratinocytes. Our findings suggested that wHCP may be clinically useful for preventing oral infectious diseases as a mouthwash for oral care.
[Mh] MeSH terms primary: Anti-Bacterial Agents/pharmacology
Biofilms/drug effects
Dental Caries/microbiology
Houttuynia/chemistry
Periodontal Diseases/microbiology
Plant Extracts/pharmacology
[Mh] MeSH terms secundary: Anti-Bacterial Agents/chemistry
Anti-Bacterial Agents/toxicity
Bacteria/drug effects
Cell Line
Cell Survival/drug effects
Humans
Plant Extracts/chemistry
Plant Extracts/toxicity
[Pt] Publication type:JOURNAL ARTICLE
[Nm] Name of substance:0 (Anti-Bacterial Agents); 0 (Plant Extracts)
[Em] Entry month:1702
[Cu] Class update date: 170223
[Lr] Last revision date:170223
[Js] Journal subset:IM
[Da] Date of entry for processing:160715
[St] Status:MEDLINE
[do] DOI:10.1155/2016/2581876

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[PMID]: 26949983
[Au] Autor:Xiao SJ; Guo DL; Zhang MS; Chen F; Ding LS; Zhou Y
[Ad] Address:a School of Pharmacy , Zunyi Medical Universty , Zunyi 563000 , China.
[Ti] Title:Three new oxazoline alkaloids from Gymnotheca chinensis.
[So] Source:J Asian Nat Prod Res;18(8):719-23, 2016 Aug.
[Is] ISSN:1477-2213
[Cp] Country of publication:England
[La] Language:eng
[Ab] Abstract:Three novel oxazoline alkaloids, 1-oxa-3-azaspiro [4.5] dec-2-ene-8-one (1), 1-oxa-3-azaspiro [4.5] dec-2, 6-diene-8-one (2), and 1-oxa-3-azaspiro [4.5] dec-10-methoxy-2, 6-diene-8-one (3) were isolated from the methanol extract of the whole plant of Gymnotheca chinensis. The chemical structures were established by means of spectroscopic analysis including one- and two-dimensional NMR spectroscopy.
[Mh] MeSH terms primary: Alkaloids/isolation & purification
Oxazoles/isolation & purification
Saururaceae/chemistry
Spiro Compounds/isolation & purification
[Mh] MeSH terms secundary: Alkaloids/chemistry
Magnetic Resonance Spectroscopy
Molecular Structure
Oxazoles/chemistry
Spiro Compounds/chemistry
Stereoisomerism
[Pt] Publication type:JOURNAL ARTICLE
[Nm] Name of substance:0 (1-oxa-3-azaspiro(4.5)dec-10-methoxy-2,6-diene-8-one); 0 (1-oxa-3-azaspiro(4.5)dec-2,6-diene-8-one); 0 (1-oxa-3-azaspiro(4.5)dec-2-ene-8-one); 0 (Alkaloids); 0 (Oxazoles); 0 (Spiro Compounds)
[Em] Entry month:1701
[Cu] Class update date: 170104
[Lr] Last revision date:170104
[Js] Journal subset:IM
[Da] Date of entry for processing:160308
[St] Status:MEDLINE
[do] DOI:10.1080/10286020.2016.1146255


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