Escobajos de la vid como fuente de compuestos fenólicos con propiedades antioxidantes

Winemaking industry generates considerable amounts of bunch stems that are usually wasted despite their potential value as source of bioactive compounds. Phenolic profiles and antioxidant capacity (AC) of bunch stem extracts from eight grape varieties of Vitis vinifera L. were determined. Sixteen phenolic compounds (PC) were quantified by high performance-liquid chromatography-diode array detection (HPLC-DAD). The maximum concentrations corresponded to the flavanols (+)-catechin (6462 μg g-1 DW) and procyanidin B1 (1987 μg g-1 DW), followed by the hydroxycinnamic acid caftaric acid (2967 μg g-1 DW). Naringin, myricetin and OH-tyrosol were identified for the first time in grape bunch stems. Total phenolic content (TPC) of extracts, assessed as gallic acid equivalents (GAE), ranged between 47 and 125 mg GAE g-1 DW. The AC of extracts was appraised by ORAC, ABTS and DPPH assays, with a good correlation between TPC and AC when measured by ABTS and DPPH (r ≥ 0.92), while for ORAC the correlation was lower (r ≤ 0.41). Samples of cv. Malbec, the most representative variety of Argentina, presented the highest contents in PC, particularly flavanols. The results showed that grape bunch stems may be an inexpensive, sustainable and high value source of bioactive compounds as functional ingredients.La industria vitivinícola genera cantidades considerables de escobajo que generalmente se desperdician a pesar de su valor potencial como fuente de compuestos bioactivos. En este trabajo se determinaron los perfiles fenólicos y capacidad antioxidantes (CA) de extractos de escobajo de ocho variedades diferentes de Vitis vinífera L. Se cuantificaron 16 compuestos fenólicos (PC) utilizando cromatografía líquida de alta resolución acoplada a detector de arreglo de diodos (HPLC-DAD). Las concentraciones más elevadas obtenidas correspondieron a los flavanoles (+)-catequina (6462 μg g-1 peso seco) y procianidina B1 (1987 μg g-1 peso seco), seguido del ácido caftárico (2967 μg g-1 peso seco). La naringenina, miricetina y OH-tirosol fueron identificados por primera vez en escobajos. El contenido total de compuestos fenólicos (TPC) de los extractos determinado con equivalentes de ácido gálico (GAE) presentó valores entre 47 y 125 mg GAE g-1 peso seco. La CA de los extractos fue determinada mediante las técnicas ORAC, ABTS y DPPH, evidenciando una buena correlación entre TPC y la CA medida mediante ABTS y DPPH (r ≥ 0,92), mientras que para ORAC la correlación fue más baja (r ≤ 0,41). La muestra de variedad más representativa de Argentina, cv. Malbec, presentó los mayores niveles de PC, particularmente flavanoles. Los resultados evidencian que los escobajos pueden ser una fuente económica, sostenible y de alto valor de compuestos bioactivos para su utilización como ingredientes funcionales.Fil: Ferreyra, Susana Gisela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Biología Agrícola de Mendoza. Universidad Nacional de Cuyo. Facultad de Ciencias Agrarias. Instituto de Biología Agrícola de Mendoza; ArgentinaFil: Bottini, Ambrosio Rubén. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Biología Agrícola de Mendoza. Universidad Nacional de Cuyo. Facultad de Ciencias Agrarias. Instituto de Biología Agrícola de Mendoza; Argentina. Universidad "Juan Agustín Maza"; ArgentinaFil: Fontana, Ariel Ramón. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Biología Agrícola de Mendoza. Universidad Nacional de Cuyo. Facultad de Ciencias Agrarias. Instituto de Biología Agrícola de Mendoza; Argentin

New fungal sources for α-L-Rhamnosidase: an important enzyme used in the synthesis of drugs and drug precursors

Two fungal strains were isolated and tentatively identified as Penicillium VY and Aspergillus VY. All the isolated species show the maximum production on third day in a liquid culture media. The pH optimum was found to be 10.0 for Penicillium VY and 11.0 for Aspergillus VY. The temperature optima were 50ºC in both the cases. The enzyme produced by Penicillium VY was found to be stable in the pH range 3.0-7.0 and 3.0–6.0 in case of Aspergillus VY. The enzyme does not loose activity up to 40º C in case of Penicillium VY and 40ºC in case of Aspergillus VY if exposed for 1 h.
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The Protective Effect of Naringin against Bleomycin-Induced Pulmonary Fibrosis in Wistar Rats

The aim of the current study was to investigate the protective effect of naringin on bleomycin-induced pulmonary fibrosis in rats. Twenty-four Wistar rats randomly divided into four groups (control, bleomycin alone, bleomycin + naringin 40, and bleomycin + naringin 80) were used. Rats were administered a single dose of bleomycin (5 mg/kg; via the tracheal cannula) alone or followed by either naringin 40 mg/kg (orally) or naringin 80 mg/kg (orally) or water (1 mL, orally) for 14 days. Rats and lung tissue were weighed to determine the lung index. TNF-α and IL-1β levels, hydroxyproline content, and malondialdehyde (MDA) levels were assayed. Glutathione peroxidase (GSH-Px) and superoxide dismutase (SOD) activities were determined. Tissue sections were stained with hematoxylin-eosin, Masson’s trichrome, and 0.1% toluidine blue. TNF-α, IL-1β, and MDA levels and hydroxyproline content significantly increased (p<0.01) and GPx and SOD activities significantly decreased in bleomycin group (p<0.01). Naringin at a dose of 80 mg/kg body weight significantly decreased TNF-α and IL-1β activity, hydroxyproline content, and MDA level (p<0.01) and increased GPx and SOD activities (p<0.05). Histological evidence supported the results. These results show that naringin has the potential of reducing the toxic effects of bleomycin and may provide supportive therapy for conventional treatment methods for idiopathic pulmonary fibrosis

Graminex pollen: phenolic pattern, colorimetric analysis and protective effects in immortalized prostate cells (PC3) and rat prostate challenged with LPS

Prostatitis, a general term describing prostate inflammation, is a common disease that could be sustained by bacterial or non-bacterial infectious agents. The efficacy of herbal extracts with antioxidant and anti-inflammatory effects for blunting the burden of inflammation and oxidative stress, with possible improvements in clinical symptoms, is under investigation. Pollen extracts have been previously reported as promising agents in managing clinical symptoms related to prostatitis. The aim of the present work was to evaluate the protective effects of Graminex pollen (GraminexTM, Deshler, OH, USA), a commercially available product based on standardized pollen extracts, in rat prostate specimens, ex vivo. In this context, we studied the putative mechanism of action of pollen on multiple inflammatory pathways, including the reduction of prostaglandin E2 (PGE2), nuclear factor kappa-light-chain-enhancer of activated B cells (NFB), and malondialdehyde (MDA), whose activities were significantly increased by inflammatory stimuli. We characterized by means of chromatographic and colorimetric studies the composition of Graminex pollen to better correlate the activity of pollen on immortalized prostate cells (PC3), and in rat prostate specimens challenged with Escherichia coli lipopolysaccharide (LPS). We found that Graminex pollen was able to reduce radical oxygen species (ROS) production by PC3 cells and MDA, NFB mRNA, and PGE2 levels, in rat prostate specimens. According to our experimental evidence, Graminex pollen appears to be a promising natural product for the management of the inflammatory components in the prostate

Therapeutic potentials of naringin on polymethylmethacrylate induced osteoclastogenesis and osteolysis, in vitro and in vivo assessments

A grant from the One-University Open Access Fund at the University of Kansas was used to defray the author’s publication fees in this Open Access journal. The Open Access Fund, administered by librarians from the KU, KU Law, and KUMC libraries, is made possible by contributions from the offices of KU Provost, KU Vice Chancellor for Research & Graduate Studies, and KUMC Vice Chancellor for Research. For more information about the Open Access Fund, please see http://library.kumc.edu/authors-fund.xml.Wear debris associated periprosthetic osteolysis represents a major pathological process associated with the aseptic loosening of joint prostheses. Naringin is a major flavonoid identified in grapefruit. Studies have shown that naringin possesses many pharmacological properties including effects on bone metabolism. The current study evaluated the influence of naringin on wear debris induced osteoclastic bone resorption both in vitro and in vivo. The osteoclast precursor cell line RAW 264.7 was cultured and stimulated with polymethylmethacrylate (PMMA) particles followed by treatment with naringin at several doses. Tartrate resistant acid phosphatase (TRAP), calcium release, and gene expression profiles of TRAP, cathepsin K, and receptor activator of nuclear factor-kappa B were sequentially evaluated. PMMA challenged murine air pouch and the load bearing tibia titanium pin-implantation mouse models were used to evaluate the effects of naringin in controlling PMMA induced bone resorption. Histological analyses and biomechanical pullout tests were performed following the animal experimentation. The in vitro data clearly demonstrated the inhibitory effects of naringin in PMMA induced osteoclastogenesis. The naringin dose of 10 µg/mL exhibited the most significant influence on the suppression of TRAP activities. Naringin treatment also markedly decreased calcium release in the stimulated cell culture medium. The short-term air pouch mouse study revealed that local injection of naringin ameliorated the PMMA induced inflammatory tissue response and subsequent bone resorption. The long-term tibia pin-implantation mouse model study suggested that daily oral gavage of naringin at 300 mg/kg dosage for 30 days significantly alleviated the periprosthetic bone resorption. A significant increase of periprosthetic bone volume and regaining of the pin stability were found in naringin treated mice. Overall, this study suggests that naringin may serve as a potential therapeutic agent to treat wear debris associated osteolysis

NARINGIN AND RUTIN PREVENT D-GALACTOSAMINE-INDUCED HEPATIC INJURY IN RATS VIA ATTENUATION OF THE INFLAMMATORY CASCADE AND OXIDATIVE STRESS

The dried stems and leaves of Citrus jambhiri Lush. (Rutaceae) were extracted with aqueous methanol and the extracts were fractionated using light petroleum, chloroform and ethyl acetate. Column chromatography of the ethyl acetate fractions resulted in the isolation of naringin, rutin, hesperidin, and neohesperidin. Their structures were identified by MS and different NMR techniques. Liquid chromatography-electrospray ionization-mass spectrometry (LC-ESI-MS) of these fractions allowed the identification 7 flavonoid glycosides. Hepatoprotective properties of naringin and rutin were evaluated in d-galactosamine (d-GalN)-induced hepatic injury in rats. d-GalN increased serum aminotransferase activity, total bilirubin, liver tumor necrosis factor-α level (TNF-α), hepatic lipid peroxidation, nuclear factor κB and decreased hepatic glutathione content, IL-10 levels and the IL-10/TNF-α ratio. These changes were attenuated in rats pretreated with rutin and naringin (40 mg/kg body weight). They increased liver IL-10 levels and the IL-10/TNF-α ratio. Rutin but not naringin down-regulated NF-κB gene expression and decreased gamma-glutamyltransferase (GGT) activity

Združeni učinci valproata i naringina na antioksidacijske i serumske pokazatelje bubrežne funkcije u miševa soja C57BL6

Valproate is known to disturb the kidney function, and high doses or prolonged intake may cause serum ion imbalance, kidney tubular acidosis, proteinuria, hyperuricosuria, polyuria, polydipsia, and dehydration. The aim of this in vivo study was to see whether naringin would counter the adverse effects of high-dose valproate in C57Bl/6 mice and to which extent. As expected, valproate (150 mg/kg bw a day for 10 days) caused serum hyperkalaemia, more in male than female mice. Naringin reversed (25 mg/kg bw a day for 10 days) the hyperkalaemia and activated antioxidative defence mechanisms (mainly catalase and glutathione), again more efficiently in females. In males naringin combined with valproate was not as effective and even showed some prooxidative effects.Valproat je jedan od najčešće primjenjivanih antiepileptika, a poznato je da prouzročuje poremećenu funkciju proksimalnih bubrežnih tubula. Fiziološki poremećaji i nefrotoksični učinci u nekih bolesnika nakon visokih doza ili produljenog uzimanja valproata uključuju disbalans iona u serumu, bubrežnu tubularnu acidozu, proteinuriju, hiperurikozuriju, poliuriju, polidipsiju, dehidraciju i druge poremećaje. U okviru ovog eksperimentalnog rada primijenili smo visoke doze valproata i združeni tretman valproata i naringina u C57Bl/6 miševa. Naringin je poznati antioksidans i protuupalna flavonoidna molekula iz citrusnog voća. Cilj rada bio je utvrditi mogu li biološka svojstva naringina umanjiti štetne učinke na bubrege nakon tretmana valproatom. Valproat je in vivo prouzročio serumsku hiperkalijemiju, izraženiju u mužjaka nego u ženki miševa. Hiperkalijemija prouzročena valproatom bila je ublažena naringinom, a antioksidacijski obrambeni mehanizmi (uglavnom katalaza i smanjena glutationacija) bili su aktivirani, više u ženki. U mužjaka, zajednički tretman valproatom I naringinom nije bio tako učinkovit, a rezultati upućuju na moguće prooksidacijsko djelovanje u bubrežnom tkivu kada se obje tvari primjenjuju zajedno

Hematological alterations in diabetic rats

Dysfunction in adipocytes is associated with insulin resistance and type 2 diabetes. Diabetes-associated anemia has been reported due to the increased non-enzymatic glycosylation of RBC membrane proteins, which correlates with hyperglycemia. The present study was hypothesized to assess the effect of citrus flavonoids on hematological parameters and adipose tissue interleukin-6 and adiponectin in type 2 diabetic rats. Diabetes was induced by feeding rats with a high fat diet for 2 weeks followed by an intraperitoneal injection of streptozotocin. An oral dose of 50 mg/kg hesperidin or naringin was daily given for 4 weeks after diabetes induction. By the end of the experiment, blood samples were collected and were immediately used for determination of haematological parameters. Expression levels of adiponectin and interleukin-6 were assayed in adipose tissue samples. Both hesperidin and naringin significantly improved the levels of erythrocytes, leukocytes and their functional indices. Similarly, supplementation with either compound significantly ameliorated the declined adipose tissue adiponectin expression in conjunction with down-regulated interleukin-6. The findings of the present study indicated that hesperidin and naringin exert protection to diabetes-associated anemia in type 2 diabetic rats. This could be due to attenuation of proinflammatory cytokine production and stimulation of adiponectin expression

A novel ultradeformable liposomes of Naringin for anti-inflammatory therapy

Ultradeformable liposomes were formulated using naringin (NA), a flavanone glycoside, at different concentrations (3,6 and 9 mg/mL). Nanovesicles were small size (∼100 nm), regardless of the NA concentration used, and monodisperse (PI < 0.30). All formulations showed a high entrapment efficiency (∼88%) and a highly negative zeta potential (around −30 mV). The selected formulations were highly biocompatible as confirmed by in vitro studies using 3T3 fibroblasts. In vitro assay showed that the amounts (%) of NA accumulated in the epidermis (∼10%) could explain the anti-inflammatory properties of ultradeformable liposomes. In vivo studies confirmed the higher effectiveness of ultradeformable liposomes respect to betamethasone cream and NA dispersion in reducing skin inflammation in mice. Overall, it can conclude that NA ultradeformable liposomes can be considered as a promising formulation for the treatment of skin inflammatory diseases