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1.
Molecules ; 22(12)2017 Dec 07.
Artigo em Inglês | MEDLINE | ID: mdl-29215592

RESUMO

Angelica gigas Nakai (AGN) is a crucial oriental medicinal herb that grows especially in Korea and the Far-East countries. It contains chemically active compounds like pyranocoumarins, polyacetylenes and essential oils, which might be useful for treatment of several chronic diseases. It has been used for centuries as a traditional medicine in Southeast Asia, but in Western countries is used as a functional food and a major ingredient of several herbal products. The genus Angelica is also known as 'female ginseng' due to its critical therapeutic role in female afflictions, such as gynecological problems. However, it is well-documented that the AGN pyranocoumarins may play vital beneficial roles against cancer, neurodisorders, inflammation, osteoporosis, amnesia, allergies, depression, fungi, diabetes, ischemia, dermatitis, reactive oxygen species (ROS) and androgen. Though numerous studies revealed the role of AGN pyranocoumarins as therapeutic agents, none of the reviews have published their molecular mechanism of action. To the best of our knowledge, this would be the first review that aims to appraise the biosynthesis of AGN's major active pyranocoumarins, discuss effective extraction and formulation methods, and detail the molecular action mechanism of decursin (D), decursinol angelate (DA) and decursinol (DOH) in chronic diseases, which would further help extension of research in this area.


Assuntos
Angelica/química , Antineoplásicos Fitogênicos/farmacologia , Medicamentos de Ervas Chinesas/farmacologia , Neoplasias/tratamento farmacológico , Fitoterapia/métodos , Piranocumarinas/farmacologia , Angelica sinensis , Animais , Antineoplásicos Fitogênicos/biossíntese , Antineoplásicos Fitogênicos/isolamento & purificação , Antineoplásicos Fitogênicos/farmacocinética , Benzopiranos/isolamento & purificação , Benzopiranos/metabolismo , Benzopiranos/farmacocinética , Benzopiranos/farmacologia , Butiratos/isolamento & purificação , Butiratos/metabolismo , Butiratos/farmacocinética , Butiratos/farmacologia , Modelos Animais de Doenças , Medicamentos de Ervas Chinesas/química , Medicamentos de Ervas Chinesas/farmacocinética , Humanos , Extração Líquido-Líquido/métodos , Medicina Tradicional Coreana , Neoplasias/genética , Neoplasias/metabolismo , Neoplasias/patologia , Extratos Vegetais/química , Raízes de Plantas/química , Plantas Medicinais , Piranocumarinas/isolamento & purificação , Piranocumarinas/metabolismo , Piranocumarinas/farmacocinética , Roedores
2.
Int J Mol Sci ; 18(11)2017 Nov 15.
Artigo em Inglês | MEDLINE | ID: mdl-29140303

RESUMO

Oxidosqualene cyclases (OSCs) are enzymes that play a key role in control of the biosynthesis of phytosterols and triterpene saponins. In order to uncover OSC genes from Polygala tenuifolia seedlings induced by methyl jasmonate (MeJA), RNA-sequencing analysis was performed using the Illumina sequencing platform. A total of 148,488,632 high-quality reads from two samples (control and the MeJA treated) were generated. We screened genes related to phytosterol and triterpene saponin biosynthesis and analyzed the transcriptional changes of differentially expressed unigene (DEUG) values calculated by fragments per kilobase million (FPKM). In our datasets, two full-length cDNAs of putative OSC genes, PtCAS1, and PtCAS2, were found, in addition to the PtBS (ß-amyrin synthase) gene reported in our previous studies and the two cycloartenol synthase genes of P. tenuifolia. All genes were isolated and characterized in yeast cells. The functional expression of the two PtCAS genes in yeast cells showed that the genes all produce a cycloartenol as the sole product. When qRT-PCR analysis from different tissues was performed, the expressions of PtCAS1 and PtCAS2 were highest in flowers and roots, respectively. After MeJA treatment, the transcripts of PtCAS1 and PtCAS2 genes increased by 1.5- and 2-fold, respectively. Given these results, we discuss the potential roles of the two PtCAS genes in relation to triterpenoid biosynthesis.


Assuntos
Transferases Intramoleculares/metabolismo , Fitosteróis/biossíntese , Polygala/enzimologia , Acetatos/farmacologia , Sequência de Aminoácidos , Ciclopentanos/farmacologia , Perfilação da Expressão Gênica , Regulação da Expressão Gênica de Plantas/efeitos dos fármacos , Genes de Plantas , Transferases Intramoleculares/química , Transferases Intramoleculares/genética , Repetições de Microssatélites/genética , Anotação de Sequência Molecular , Oxilipinas/farmacologia , Filogenia , Fitosteróis/química , Polygala/efeitos dos fármacos , Polygala/genética , Saccharomyces cerevisiae/metabolismo , Plântula/efeitos dos fármacos , Plântula/genética , Transcriptoma/genética
3.
Molecules ; 22(9)2017 Aug 31.
Artigo em Inglês | MEDLINE | ID: mdl-28858245

RESUMO

Ixeris dentata var. albiflora is considered as a potential therapeutic agent against mithridatism, calculous, indigestion, pneumonia, hepatitis, and tumors as well as good seasoned vegetable in Far East countries. Phytoene synthase (PSY), phytoene desaturase (PDS) ξ-carotene desaturase (ZDS), lycopene ß-cyclase (LCYB), lycopene ε-cyclase (LCYE), ε-ring carotene hydroxylase (CHXB), and zeaxanthin epoxidase (ZDS) are vital enzymes in the carotenoid biosynthesis pathway. We have examined these seven genes from I. dentata that are participated in carotenoid biosynthesis utilizing an Illumina/Solexa HiSeq 2000 platform. In silico analysis of the seven deduced amino acid sequences were revealed its closest homology with other Asteracea plants. Further, we explored transcript levels and carotenoid accumulation in various organs of I. dentata using quantitative real time PCR and high-performance liquid chromatography, respectively. The highest transcript levels were noticed in the leaf for all the genes while minimal levels were noticed in the root. The maximal carotenoid accumulation was also detected in the leaf. We proposed that these genes expressions are associated with the accumulation of carotenoids. Our findings may suggest the fundamental clues to unravel the molecular insights of carotenoid biosynthesis in various organs of I. dentata.


Assuntos
Asteraceae/genética , Carotenoides/biossíntese , Proteínas de Plantas/genética , Asteraceae/metabolismo , Vias Biossintéticas , Clonagem Molecular , Expressão Gênica , Proteínas de Plantas/biossíntese , Raízes de Plantas/genética , Raízes de Plantas/metabolismo
4.
Chem Biol Interact ; 254: 146-55, 2016 Jul 25.
Artigo em Inglês | MEDLINE | ID: mdl-27154496

RESUMO

This study was conducted to investigate the protective effect of red paprika extract (RPE) and its main carotenoids, namely, capsanthin (CST) and ß-carotene (BCT), on the H2O2-induced inhibition of gap-junction intercellular communication (GJIC) in WB-F344 rat liver epithelial cells (WB cells). We found that pre-treatment with RPE, CST and BCT protected WB cells from H2O2-induced inhibition of GJIC. RPE, CST and BCT not only recovered connexin 43 (Cx43) mRNA expression but also prevented phosphorylation of Cx43 protein by H2O2 treatment. RPE attenuated the phosphorylation of ERK, p38 and JNK, whereas pre-treatment with CST and BCT only attenuated the phosphorylation of ERK and p38 and did not affect JNK in H2O2-treated WB cells. RPE, CST and BCT significantly suppressed the formation of reactive oxygen species (ROS) in H2O2-treated cells compared to untreated WB cells. These results suggest that dietary intake of red paprika might be helpful for lowering the risk of diseases caused by oxidative stress.


Assuntos
Capsicum/química , Comunicação Celular/efeitos dos fármacos , beta Caroteno/farmacologia , Animais , Capsicum/metabolismo , Linhagem Celular , Sobrevivência Celular/efeitos dos fármacos , Conexina 43/genética , Conexina 43/metabolismo , Células Epiteliais/citologia , Células Epiteliais/efeitos dos fármacos , Células Epiteliais/metabolismo , Junções Comunicantes/efeitos dos fármacos , Junções Comunicantes/metabolismo , Peróxido de Hidrogênio/toxicidade , Proteínas Quinases JNK Ativadas por Mitógeno/metabolismo , Proteína Quinase 1 Ativada por Mitógeno/metabolismo , Proteína Quinase 3 Ativada por Mitógeno/metabolismo , Estresse Oxidativo/efeitos dos fármacos , Fosforilação/efeitos dos fármacos , Extratos Vegetais/química , Extratos Vegetais/farmacologia , Ratos , Ratos Endogâmicos F344 , Espécies Reativas de Oxigênio/metabolismo , Xantofilas/farmacologia , Proteínas Quinases p38 Ativadas por Mitógeno/metabolismo
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