Efeito quimiopreventivo da Beta-ionona na hepatocarcinogênese associada à fibrose hepática / Chemopreventive effect of Beta-ionone in hepatocarcinogenesis associated with hepatic fibrosis

O carcinoma hepatocelular (HCC) é a neoplasia primária mais frequente que acomete o fígado, a quarta principal causa de morte relacionada ao câncer e apresenta mau prognóstico. A fibrose hepática está presente em grande parte dos casos de HCC e é um dos principais fatores de risco para esta afecção. Segundo estudos prévios do grupo, a ß-ionona (BI), presente em uvas e aromatizantes de vinho, apresenta potencial quimiopreventivo na hepatocarcinogênese principalmente por reduzir o número e tamanho de lesão pré neoplásica (LPN) e inibir a proliferação celular. No entanto, até o presente não foram identificados na literatura estudos que investigaram o efeito deste isoprenóide no processo fibrótico e na hepatocarcinogênese a ele associada. Desta forma, este estudo pretendeu investigar o potencial efeito quimiopreventivo da BI na hepatocarcinogênese associada à fibrose hepática. Para tanto, ratos machos Wistar foram tratados com óleo de milho (OM) [0,25 ml / 100 g de peso corporal (p.c.); Grupo de OM] ou BI (16mg / 100g p.c.; Grupo BI) durante 18 semanas. A partir da 2ª semana, todos os animais receberam uma dose intraperitoneal de dietilnitrosamina (DEN - 50 mg / Kg p.c.) uma vez por semana até a 16ª semana. Os animais foram eutanasiados em diferentes períodos do protocolo experimental: na 10a semana (grupos OMP1 e BIP1), na 14a semana (grupos OMP2 e BIP2) e na 18ª semana (grupos OMP3 e BIP3). O isoprenóide demonstrou, de maneira inédita na literatura, inibir o desenvolvimento da fibrose hepática em diferentes estágios da hepatocarcinogênese (pontos 1, 2 e 3) por reduzir (p < 0,05) a porcentagem de área marcada para picrosirius. Além disso, BI reduziu a porcentagem de área positiva para α- SMA (p < 0,05) e as concentrações de hidroxiprolina (p < 0,05) no ponto 2. Foi observada ação quimiopreventiva da BI nas fases iniciais da hepatocarcinogênese (pontos 1 e 2) mesmo em modelo associada a fibrose por reduzir (p < 0,05) o número e porcentagem de área do corte ocupada por LPN GSTP positivas. Este efeito não foi observado em fase mais avançada da hepatocarcinogênese (ponto 3). Corroborando este dado não foram observadas diferenças em relação ao número de tumores (p>=0,05) avaliados por imageamento e por análise histopatológica. No entanto, quando comparados ao seu controle (OMP3), os animais do grupo BIP3 apresentaram menor mortalidade e menor incidência (p < 0,05) de HCC high, considerado um tipo mais agressivo de HCC, sugerindo que este composto possa atuar na agressividade das células tumorais. O grupo BIP2 demonstrou ainda menor proliferação celular (p < 0,05) quando comparado ao grupo OMP2. Assim foram avaliadas as vias de proliferação celular PI3K/AKT e MAPK/ERK, bem como as proteínas p21 e p53, relacionadas a progressão do ciclo celular. Não foram observadas(p≥0,05) alterações nestas vias por parte do isoprenóide. O presente estudo demonstrou ação protetora da BI no desenvolvimento de fibrose, bem como na hepatocarcinogênese a ela associada. Contudo, são necessárias análises complementares para elucidar mecanismos pelos quais a BI atua na carcinigênese hepática associada à fibrose

Hepatocellular carcinoma (HCC) is the primary liver cancer, the fourth leading cause of death related to cancer and presents a poor prognosis. Hepatic fibrosis is present in most cases of HCC and represents one of the main risk factors for this condition. According to previous studies of the group, ß-ionone (BI), present in grapes and wine flavorings, has a potential chemopreventive in hepatocarcinogenesis mainly by reducing the number and size of preneoplastic lesions (LPN) and inhibiting cell proliferation. However, to date, no studies have been identified in the literature that investigated the effect of this isoprenoid on the fibrotic process and in its association with hepatocarcinogenesis. Thus, this study aimed to investigate the potential chemopreventive effect of BI in hepatocarcinogenesis associated with hepatic fibrosis. Male Wistar rats were treated with corn oil (OM) [0.25 ml / 100 g body weight (b.w.); OM] or BI group (16mg / 100g b.w; BI group) for 18 weeks. From week 2, all animals received an intraperitoneal dose of diethylnitrosamine (DEN - 50 mg / kg b.w.) once in a week until week 16. The animals were euthanized at different periods of the experimental protocol: at week 10 (groups OMP1 and BIP1), at week 14 (groups OMP2 and BIP2) and week 18 (groups OMP3 and BIP3). The isoprenoid, for the first time in the literature, shown to inhibit the development of liver fibrosis at different stages of hepatocarcinogenesis (points 1, 2 and 3) by reducing (p <0.05) the percentage of the area labeled for picrosirius. Also, BI reduced the percentage of α-SMA positive area (p <0.05) and hydroxyproline concentrations (p <0.05) at point 2. BI chemopreventive action was observed in the early stages of hepatocarcinogenesis (point 1 and 2) even in a model associated with fibrosis for reducing (p <0.05) the number and percentage of the liver section area occupied by GSTP positive LPN. This effect was not observed at a later stage of hepatocarcinogenesis (point 3). Corroborating this data, no differences were observed regarding the number of tumors (p>=0.05) evaluated by imaging and histopathological analysis. However, when compared to its control (OMP3), animals from the BIP3 group had lower mortality and lower incidence (p<0.05) of HCC high, considered a more aggressive type of HCC, suggesting that this compound may act in aggressiveness of tumor cells. The BIP2 group also showed lower cell proliferation (p <0.05) when compared to the OMP2 group. Thus, PI3K / AKT and MAPK / ERK cell proliferation pathways were evaluated, as well as p21 and p53 proteins, related to cell cycle progression. No changes were observed in these pathways by the isoprenoid (p≥0.05). The present study demonstrated the protective action of BI in the development of fibrosis, as well as its association with hepatocarcinogenesis. However, further analysis is needed to elucidate mechanisms by which BI acts on fibrosis-associated liver carcinogenesis

Chemical constituents from aerial parts of Hypoestes phyllostachya / 中草药

Objective To study the chemical constituents from the aerial parts of Hypoestes phyllostachya. Methods The compounds were isolated and purified by silica gel column chromatography, MCI, and HPLC. Their structures were elucidated by spectroscopic analysis. Results Eighteen compounds were isolated from 95% ethanol aqueous extract of H. phyllostachya and the structures were identified as (3R,6R,7E)-3-hydroxy-megastigma-4,7-dien-9-one (1), (3S)-3-hydroxy-β-ionone (2), (3S,5R,6S,7E)-5,6-epoxy-3- hydroxy-megastigma-7-en-9-one (3), grasshopper ketone (4), vomifoliol (5), (+)-dehydrovomifoliol (6), loliolide (7), 2,6-dimethyl- 2E,7-octadien-1,6-diol (8), bifurcanol (9), (12S)-hydroxygeranylgeraniol (10), nectandrin B (11), N-trans-feruloyltyramine (12), syringylethanone (13), paeonol (14), vanillin (15), dehydrozingerone (16), 2-hydroxybenzyl alcohol (17), and (2E)-4-hydroxy-2- hexenoic acid (18). Conclusion All compounds are isolated from this plant for the first time.

Efeito quimiopreventivo da ß-ionona nas fases de iniciação e seleção/promoção da hepatocarcinogênese associada ao desenvolvimento de esteatose hepática não alcoólica em ratos Wistar / Chemopreventive effect of ß-ionone in the phases of initiation and selection/promotion of hepatocarcinogenesis associated with the development of non-alcoholic steatosis in Wistar rats

O câncer é um dos principais problemas de saúde pública no mundo. Dentre as neoplasias primárias que acometem o fígado, o carcinoma hepatocelular (HCC) é a mais frequente. Diversos fatores de risco predispõem ao HCC, entre eles a doença hepática gordurosa não-alcoólica (NAFLD). Segundo estudos prévios do grupo, a ß-ionona (BI), presente em uvas e aromatizantes de vinho, apresenta potencial quimiopreventivo da hepatocarcinogênese. Além disso, a ßI parece atuar na redução da colesterolemia podendo, assim, influenciar a NAFLD. Desta forma pretendeu-se, neste projeto, avaliar o desenvolvimento da NAFLD e sua influência nas etapas de iniciação e seleção/promoção da hepatocarcinogênese em ratos Wistar submetidos ao modelo do hepatócito resistente (RH), além da atividade quimiopreventiva da ßI, nessas condições experimentais em ratos. Para isso, os animais foram alocados em 6 grupos experimentais: RH iniciação (n=11), NAFLD iniciação (n=15), BI iniciação (n=15), RH seleção/promoção (n=11), NAFLD seleção promoção (n=15) e BI seleção/promoção (n=15). Na fase de iniciação os animais do grupo NAFLD receberam, diariamente, emulsão hipercalórica até a sexta semana do experimento um dia antes da administração de DEN. Já na fase de seleção/promoção os animais do grupo NAFLD receberam a emulsão hipercalórica, a partir de um dia após a DEN. Os animais dos grupos RH da iniciação e da seleção/promoção servem como controles e receberam, diariamente, 1mL/100g peso corpóreo de água até a sexta semana do experimento e um dia após a DEN, respectivamente. Na fase de iniciação, após 13 semanas os animais do grupo NAFLD não demonstraram sinais de esteatose, apresentaram maiores níveis séricos de triacilglicerol, colesterol total e LDL comparados ao grupo RH (P<0,05). O grupo NAFLD apresentou maior porcentagem de nódulos macroscópicos, bem como maior número e porcentagem de área hepática de lesões pré neoplásicas persistentes (pLPN) comparado ao grupo RH (P<0,05). Já o grupo BI apresentou menor número de pLPN e maior número de lesões em remodelação e uma maior porcentagem de área hepática de rLPN (p<0,05). Em relação a proliferação celular, o grupo NAFLD apresentou maior número de células em sourrounding, pLPN e rLPN comparada ao grupo RH e o grupo BI menor número em pLPN comparada a NAFLD. Já na fase de seleção/promoção foi possível observar o grupo NAFLD tem maiores valores de focos de inflamação, hepatócitos balonizados e grau de esteatose hepática em relação ao grupo BI, assim como maiores níveis séricos de triacilgliceróis, colesterol total e LDL (p<0,05). O grupo NAFLD apresentou maior porcentagem de nódulos macroscópicos <1, maior número, menor tamanho médio de pLPN comparados ao grupo RH (p<0,05). O grupo BI apresentou menor número e menor porcentagem de área em pLPN e maior porcentagem de área em rLPN (p<0,05). Em relação a proliferação celular, o grupo NAFLD apresentou maior número de células em sourrounding, pLPN e rLPN comparada ao grupo RH (p<0,05). Na expressão gênica, o grupo BI apresentou maior expressão de HMGCR em relação grupo NAFLD (p<0,05), O grupo NAFLD apresentou maior expressão de INSIG1 em relação ao grupo RH (p<0,05) e tendência na expressão de INSIG 2

Cancer is a major public health problems in the world. Among the primary neoplasm affecting the liver, hepatocellular carcinoma (HCC) is the most frequent. Several risk factors predispose to HCC, including the non-alcoholic fatty liver disease (NAFLD). According to previous studies of the group, ß-ionone (BI), present in grapes and flavors of wine, it presents potential chemopreventive of hepatocarcinogenesis. Furthermore, ßI appears to act in reducing blood cholesterol and may thus influence NAFLD. In this way it was intended in this project, evaluate the development of NAFLD and its influence on the steps of initiation and selection/promotion of hepatocarcinogenesis in Wistar rats resistant hepatocyte model (HR), and the chemopreventive activity of ßI, these experimental conditions in rats. For this, the animals were divided into 6 groups: RH initiation (n = 11), NAFLD initiation (n = 15), BI initiation (n = 15), HR selection / promotion (n = 11), NAFLD selection promotion ( n = 15) and BI selection / promotion (n = 15). In the inception phase of the NAFLD group animals received daily calorie emulsion until the sixth week of the experiment one day prior to DEN administration. In the selection / promotion stage NAFLD group of animals received hypercaloric emulsion, from one day after the DEN. The animals of groups HR and selection of initiation / promotion serve as controls and received daily 1mL / 100g body weight of water until the sixth week of the experiment, and one day after DEN respectively. In the initiation phase, after 13 weeks the animals of group NAFLD showed no signs steatosis, had higher serum levels of triglyceride, total cholesterol and LDL compared to the HR group (P <0.05). The NAFLD showed higher prevalence of macroscopic nodules as well as higher number and percentage of liver area of persistent pre-neoplastic lesions (pLPN) compared to the HR group (P <0.05). But the BI group had fewer pLPN and higher number of lesions in remodeling and a higher percentage of liver area rLPN (p <0.05). In relation to cell proliferation, the NAFLD group had a higher number of cells in sourrounding, pLPN and rLPN compared to the RH group and the lowest number in pLPN BI group compared to NAFLD. In the selection / promotion layer was observed NAFLD group has the highest values of inflammation foci, balonizados hepatocytes and hepatic steatosis grade in relation to BI group as well as higher serum levels of triglyceride, total cholesterol and LDL (p <0 , 05). The NAFLD showed higher prevalence of macroscopic nodules <1, more, smaller average size pLPN compared to the HR group (p <0.05). The BI group had fewer and smaller percentage area in pLPN and higher percentage of area rLPN (p <0.05). In relation to cell proliferation, the NAFLD group had a higher number of cells in sourrounding, pLPN and rLPN compared to the HR group (p <0.05). In gene expression, the BI group showed higher expression of HMGCR regarding NAFLD group (p <0.05), the NAFLD group had higher expression of INSIG1 against the RH group (p <0.05) and a tendency in the expression of INSIG 2

Chemical constituents from asplenium unilaterale / 中国药学杂志

OBJECTIVE: To study the chemical constituents from the whole plants of Asplenium unilaterale. METHODS: The methanol extract was isolated and purified by silica gel, Sephadex LH-20, and semi-preparative HPLC column chromatography. All compounds were identified on the basis of spectral analysis. RESULTS: Fifteen compounds were isolated and identified as (Z)-4-(2, 6, 6-trimethylcyclohex-2-enylidene) butan-2-ol (1), icariside B2 (2), citroside A(3), (6R, 9R)-3-oxo-α-ionol-9-O-β-D-glucopyranoside(4), (6S, 9R)-roseoside(5), 6-methyl-2H-chromen-2-one (6), 6, 7-dihydroxy-2H-1-benzopyran-2-one (7), gibepyrone D(8), lupan-3-one(9), violanthin(10), 22, 23-dimethylcholest-5-en-3-ol(11), 1-dotriacontanol (12), 5-hexylfuran-2(5H)-one(13), tocopherylquinone( 14) and 2, 4 (1H, 3H)-pyrimidinedione(15), respectively. CONCLUSION: Compounds 1-15 are isolated from the genus for the first time.

Chemical constituents from leaves of loropetalum Chinense / 中国药学杂志

OBJECTIVE: To study the chemical constituents of Loropetalum chinense leaves. METHODS: The acetone extract was isolated and purified by macroporous resin, ODS column, silica gel column and Sephadex LH-20 chromatography. All compounds were identified on the basis of spectral analysis. RESULTS: Eleven compounds were isolated from Loropetalum chinense leaves and i-dentified as β-D-glucopranosyl(Z)-3-hexenol(1), ampelopsisionoside(2), salidroside(3), 2-hydroxy-5-[3-hydroxybutyl] phenyl-β-D-glucopyranoside (4), myricetin 3-O-α-L-rhamnoside(5), 6″-O-galloylsalidroside (6), methyl chlorogenate (7), chlorogenic acid (8), myricetin-3-O-β-D-glucoside(9), alangionoside-A(10), and benzyl-α-L-rhamonopyranosyl-(1→6)-β-D-glucopyranoside(11). CONCLUSION: Compounds 1-4, 6, 10 and 11 are isolated from this genus for the first time.

Chemical constituents from marine alga Sargassum thunbergii / 中国药学杂志

OBJECTIVE: To study the chemical constituents of Sargassum thunbergii. METHODS: The compounds were isolated and purified upon extensive column chromatography using silica gel, ODS, Sephadex LH-20, and prepative HPLC, while their structures were identified on the basis of physicochemical properties and spectroscopic data analysis. RESULTS: Fifteen compounds were isolated from the EtOH extract. The structures were identified as(+)-isololiolide(1), (-)-loliolide(2), loliolide acetate(3) grasshopper ketone(4), apo-9β-fucoxanthinone(5), 3α-hydroxy-5, 6-epoxy-7-megastigmen-9-one(6), deacetylate-apo-13'-fucoxanthinone(7), apo-13'-fucoxanthinone(8),(R)-(-)-3-hydroxy-β-ionone(9) and 6 other compounds sargassum ketone(10), 2-heptenoicacid, 4,4-dihydroxy-2,3-dimethyl-7-lactone(11), (R)-2-hydroxy-3-phenylpropanamide(12), thymidine(13), fucosterol(14) and hexade-canoic acid-2β, 3β-dihydroxypropyl ester(15). CONCLUSION: Deacetylate-apo-13'-fucoxanthinone is a new compound, and compounds 3,5,6,8,9,15 are obtained from the genus Sargassum for the first time.

Efficacy of geraniol but not of β-ionone or their combination for the chemoprevention of rat colon carcinogenesis

β-ionone (βI), a cyclic isoprenoid, and geraniol (GO), an acyclic monoterpene, represent a promising class of dietary chemopreventive agents against cancer, whose combination could result in synergistic anticarcinogenic effects. The chemopreventive activities of βI and GO were evaluated individually or in combination during colon carcinogenesis induced by dimethylhydrazine in 48 3-week-old male Wistar rats (12 per group) weighing 40-50 g. Animals were treated for 9 consecutive weeks with βI (16 mg/100 g body weight), GO (25 mg/100 g body weight), βI combined with GO or corn oil (control). Number of total aberrant crypt foci (ACF) and of ACF ≥4 crypts in the distal colon was significantly lower in the GO group (66 ± 13 and 9 ± 2, respectively) compared to control (102 ± 9 and 17 ± 3) and without differences in the βI (91 ± 11 and 14 ± 3) and βI+GO groups (96 ± 5 and 19 ± 2). Apoptosis level, identified by classical apoptosis morphological criteria, in the distal colon was significantly higher in the GO group (1.64 ± 0.06 apoptotic cells/mm²) compared to control (0.91 ± 0.07 apoptotic cells/mm²). The GO group presented a 0.7-fold reduction in Bcl-2 protein expression (Western blot) compared to control. Colonic mucosa concentrations of βI and GO (gas chromatography/mass spectrometry) were higher in the βI and GO groups, respectively, compared to the control and βI+GO groups. Therefore, GO, but not βI, represents a potential chemopreventive agent in colon carcrvpdate=20110329inogenesis. Surprisingly, the combination of isoprenoids does not represent an efficient chemopreventive strategy.

The Influence of Lonone and Ergosterol on the Growth and the Yield of CoQ_(10) in Yeast / 微生物学通报

The influence of ?-ionone and ergosterol on the growth and the yield of CoQ_ 10 in yeast was investigated. The results indicated that ?-ionone had the stimulative effect on the biosynthesis of CoQ_ 10 in yeast, and 28.3% increase of the CoQ_ 10 content in the cell was observed when the concentration of ?-ionone in the medium was 0.208?10~ -3 mol/L. Little ergosterol also had the same effect with ?-ionone, while 31.3% increase of the CoQ_ 10 content in the cell was observed when the concentration of ergosterol in the medium was 0.15?10~ -4 mol/L. However, the biosynthesis of CoQ_ 10 was inhibited when the concentration of ergosterol was 0.60?10~ -4 mol/L. Addition of ?-ionone and ergosterol to the medium resulted in 36.1% increase over the control. The results showed that the cell could effectively accumulate more CoQ_ 10 with the addition of ?-ionone and ergosterol to the medium.