Mangiferin attenuates DSS colitis in mice: Molecular docking and in vivo approach.

Abstract:

:Inflammation, oxidative stress and altered mucosal barrier permeability are potential etiopathological or triggering factors for inflammatory bowel disease (IBD). In this study, the therapeutic potential of Mangiferin was investigated in vivo in mouse model of colitis and also attempts were made to understand mechanistic insights of Mangiferin in IBD. In present study, colitis was induced by administration of 5% DSS for 11 days, followed by 3 days of DSS free period. On day 14, animals were sacrificed and colon tissues were taken for biochemical and histological analysis. Therapeutic treatment with Mangiferin after colitis induction (i.e. day 5) ameliorated symptoms of colitis (presence of blood in stools, body weight loss and diarrhea) as evidenced by reduced DAI score, attenuated the levels of catalase (CAT), reduced glutathione (GSH), superoxide dismutase (SOD), malondialdehyde (MDA), myeloperoxidase (MPO). It also decreased the colonic pro-inflammatory mediators tumor necrosis factor (TNF-α), interleukin 1β (IL-1β) levels, matrix metalloproteinase-9 (MMP-9) activity and histopathological score. Molecular docking of Mangiferin against TNF-α and MMP-9 was evaluated using GLIDE software. Mangiferin demonstrated the glide score of -8.04 kcal/mol for TNF-α and -9.97 kcal/mol for MMP-9, which indicated its binding potential with TNF-α and MMP-9. In conclusion, Mangiferin reduces colonic damage in a murine model of colitis, alleviates the oxidative and inflammatory events partly through directly influencing the activity of TNF-α and MMP-9 and therefore might have therapeutic usefulness in the management of inflammatory bowel disease.

journal_name

Chem Biol Interact

authors

Somani S,Zambad S,Modi K

doi

10.1016/j.cbi.2016.04.033

subject

Has Abstract

pub_date

2016-06-25 00:00:00

pages

18-26

eissn

0009-2797

issn

1872-7786

pii

S0009-2797(16)30156-9

journal_volume

253

pub_type

杂志文章
  • A review of mechanisms underlying anticarcinogenicity by brassica vegetables.

    abstract::The mechanisms by which brassica vegetables might decrease the risk of cancer are reviewed in this paper. Brassicas, including all types of cabbages, broccoli, cauliflower and Brussels sprouts, may be protective against cancer due to their relatively high glucosinolate content. Glucosinolates are usually broken down t...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章,评审

    doi:10.1016/s0009-2797(96)03745-3

    authors: Verhoeven DT,Verhagen H,Goldbohm RA,van den Brandt PA,van Poppel G

    更新日期:1997-02-28 00:00:00

  • Lead exposure inhibits osteoblastic differentiation and inactivates the canonical Wnt signal and recovery by icaritin in MC3T3-E1 subclone 14 cells.

    abstract::Exposure to lead (Pb) poses a threat to human bone health, including changes in bone mineral composition and the inhibition of skeletal growth and bone maturation. However, little is known about how Pb directly affects osteoblasts. In this work, we found that sub-toxic Pb concentrations suppressed bone nodule formatio...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/j.cbi.2019.01.039

    authors: Sun K,Mei W,Mo S,Xin L,Lei X,Huang M,Chen Q,Han L,Zhu X

    更新日期:2019-04-25 00:00:00

  • The effects of indole-3-acetic acid on human and horse serum butyrylcholinesterase.

    abstract::Butyrylcholinesterase (BChE) constitutes the first line defense in the serum of higher organisms and is a marker for toxic exposure. Indole-3-acetic acid (IAA) is a major plant growth hormone of the auxin class, affecting cell enlargement, and differentiation. As a result of the industrial usage, this agrochemical is ...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/j.cbi.2005.10.061

    authors: Bodur E,Cokugras AN

    更新日期:2005-12-15 00:00:00

  • The in vitro metabolites of 2,4,6-trichlorophenol and their DNA strand breaking properties.

    abstract::The carcinogenic compound 2,4,6-trichlorophenol (2,4,6-TCP) was incubated with rat liver S-9 fraction. Three metabolites were identified: 2,6-dichloro-1,4-hydroquinone (DHQ), and two isomers of hydroxypentachlorodiphenyl ether (OH-Cl5-DPE). The latter are probably products of microsomal .OH radical attack on the trich...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/0009-2797(89)90119-1

    authors: Juhl U,Blum K,Witte I

    更新日期:1989-01-01 00:00:00

  • Instability of C154Y variant of aldo-keto reductase 1C3.

    abstract::Aldo-keto reductase (AKR) 1C3 is a cytosolic enzyme that metabolizes steroids, prostaglandins, toxic aldehydes and drugs. Recently, some nonsynonymous single nucleotide polymorphisms of AKR1C3 have been suggested to impact steroid and drug metabolism. In this study, we examined the effects of C154Y and L159V variants ...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/j.cbi.2016.12.018

    authors: Endo S,Takada S,Honda RP,Müller K,Weishaupt JH,Andersen PM,Ludolph AC,Kamatari YO,Matsunaga T,Kuwata K,El-Kabbani O,Ikari A

    更新日期:2017-10-01 00:00:00

  • Peroxisome proliferation and associated effects caused by perfluorooctanoic acid in vitamin A-deficient mice.

    abstract::Vitamin A-deficient male mice were treated for 10 days with 0.02% perfluorooctanoic acid (PFOA) in their diet. The effects of this highly potent peroxisome proliferator on peroxisomal palmitoyl-CoA oxidation and lauroyl-CoA oxidase activities were reduced by 3.1-7.5 times in comparison to the values obtained with mice...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/0009-2797(95)03630-5

    authors: Sohlenius AK,Andersson K,Olsson J,DePierre JW

    更新日期:1995-10-20 00:00:00

  • Anticancer activity and radiosensitization effect of methyleneisoxazolidin-5-ones in hepatocellular carcinoma HepG2 cells.

    abstract::Parthenolide (PTL), a well-known sesquiterpene lactone of natural origin with α,β-unsaturated carbonyl structure, has proven to show promising anti-cancer properties. In this report, anti-proliferative potential of two synthetic methyleneisoxazolidin-5-ones, MZ-6 and MZ-14, with the same structural motif, has been inv...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/j.cbi.2016.01.011

    authors: Gach K,Grądzka I,Wasyk I,Męczyńska-Wielgosz S,Iwaneńko T,Szymański J,Koszuk J,Janecki T,Kruszewski M,Janecka A

    更新日期:2016-03-25 00:00:00

  • In vitro glutathione peroxidase mimicry of ebselen is linked to its oxidation of critical thiols on key cerebral suphydryl proteins - A novel component of its GPx-mimic antioxidant mechanism emerging from its thiol-modulated toxicology and pharmacology.

    abstract::The antioxidant mechanism of ebselen in rats brain is largely linked with its glutathione peroxidase (GPx) rather than its peroxiredoxin mimicry ability. However, the precise molecular dynamics between the GPx-mimicry of ebselen and thiol utilization is yet to be fully clarified and thus still open. Herein, we investi...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/j.cbi.2013.07.014

    authors: Kade IJ,Balogun BD,Rocha JB

    更新日期:2013-10-25 00:00:00

  • Metabolism of 1-nitropyrene in mice: transport across the placenta and mammary tissues.

    abstract::The distribution and metabolism of the environmental pollutant 1-nitropyrene was studied in C57B1/6N mice following oral or intraperitoneal dosing. When administered by gavage, 1-nitropyrene and its metabolites demonstrated biphasic elimination kinetics from the blood, with half-lives of 0.3 and 1.8 days and a distrib...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/0009-2797(94)03574-r

    authors: Howard PC,Consolo MC,Dooley KL,Beland FA

    更新日期:1995-04-14 00:00:00

  • The role of paraoxonase (PON1) in the detoxication of organophosphates and its human polymorphism.

    abstract::In human populations, serum paraoxonase (PON1) exhibits a substrate dependent polymorphism. The Arg192 isoform hydrolyzes paraoxon rapidly but diazoxon, soman and especially sarin slowly. On the other hand, the Gln192 isoform hydrolyzes paraoxon slowly, but diazoxon, soman and sarin more rapidly than the Arg192 isofor...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章,评审

    doi:10.1016/s0009-2797(99)00055-1

    authors: Costa LG,Li WF,Richter RJ,Shih DM,Lusis A,Furlong CE

    更新日期:1999-05-14 00:00:00

  • Effect of DL-alpha-lipoic acid on mitochondrial enzymes in aged rats.

    abstract::Mitochondrial dysfunction appears to contribute to some of the loss of function accompanying ageing. Mitochondria from aged tissue use oxygen inefficiently impairing ATP synthesis and results in increased oxidant production. A high flux of oxidants not only damages mitochondria, but other important cell biomolecules a...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/s0009-2797(01)00268-x

    authors: Arivazhagan P,Ramanathan K,Panneerselvam C

    更新日期:2001-11-28 00:00:00

  • The effect of caffeine on the cytotoxicity of misonidazole and some other nitroheterocyclic compounds.

    abstract::Caffeine was found to potentiate the cytotoxic effect of misonidazole (1-(2-nitroimidazol-1-yl)-3-methoxy-2-propanol) towards mammalian cells in vitro. This enhancement of toxicity is shown to occur under both aerobic and hypoxic conditions. Split dose experiments indicate that the general shape of the hypoxic surviva...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/0009-2797(82)90089-8

    authors: Horsman MR,Stratford IJ

    更新日期:1982-08-01 00:00:00

  • Steroid hormone biotransformation and xenobiotic induction of hepatic steroid metabolizing enzymes.

    abstract::Normal reproductive development depends on the interplay of steroid hormones with their receptors at specific tissue sites. The concentrations of hormone ligands in the circulation and at target sites are maintained through coordinated regulation on steroid biosynthesis and degradation. Changed bioavailability of ster...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章,评审

    doi:10.1016/j.cbi.2004.01.006

    authors: You L

    更新日期:2004-04-15 00:00:00

  • Changes in autorhythmic heart frequency elicited by redox agents.

    abstract::In isolated frog heart it was established that methylene-blue (MB, an oxidizing agent) decreased, while ascorbate (ASC, a reducing agent) increased the frequency of autorhythmic heart contractions. After MB treatment, in parallel with this phenomenon, the extracellular K+ concentration [K+]o showed a slow increase, bu...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/0009-2797(87)90092-5

    authors: Wittmann I,Puppi A,Dely M

    更新日期:1987-01-01 00:00:00

  • The inhibition of lipid peroxidation by disulfiram prevents the killing of cultured hepatocytes by allyl alcohol, tert-butyl hydroperoxide, hydrogen peroxide and diethyl maleate.

    abstract::Disulfiram is a potent antioxidant that prevented the peroxidation of microsomal phospholipids induced by ADP/Fe3+ at concentrations as low as 1 microM. However, disulfiram had a biphasic action when used to assess the role of lipid peroxidation in the killing of cultured hepatocytes by an acute oxidative stress. At a...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/0009-2797(89)90003-3

    authors: Kyle ME,Serroni A,Farber JL

    更新日期:1989-01-01 00:00:00

  • Kinetic studies of the hydrolysis of platinum-DNA complexes by nuclease S1.

    abstract::The antitumor agent cis-diamminedichloroplatinum(II) (cis-DDP) reacts covalently with DNA and disrupts its secondary structure. Damaged DNA, but not native DNA, is readily digested by S1 nuclease, an endonuclease specific for single stranded polynucleotides. We have measured S1 nuclease digestion of platinated DNA by ...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/0009-2797(90)90003-6

    authors: Butour JL,Mazard AM,Vieussens C,Johnson NP

    更新日期:1990-01-01 00:00:00

  • Prevention of prostate cancer through custom tailoring of chemopreventive regimen.

    abstract::One practical way to control cancer is through chemoprevention, which refers to the administration of synthetic or naturally occurring agents to block, reverse or delay the process of carcinogenesis. For a variety of reasons, the most important of which is human acceptance, for chemopreventive intervention naturally o...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章,评审

    doi:10.1016/j.cbi.2007.03.001

    authors: Siddiqui IA,Afaq F,Adhami VM,Mukhtar H

    更新日期:2008-01-30 00:00:00

  • Acetaminophen hepatotoxicity and sterile inflammation: The mechanism of protection of Chlorogenic acid.

    abstract::Acetaminophen hepatotoxicity is characterized by extensive necrotic cell death and a sterile inflammatory response. A recent report suggested that a therapeutic intervention with chlorogenic acid, a dietary polyphenolic compound, protects against acetaminophen-induced liver injury by inhibiting the inflammatory injury...

    journal_title:Chemico-biological interactions

    pub_type: 信件

    doi:10.1016/j.cbi.2015.08.025

    authors: Jaeschke H

    更新日期:2016-01-05 00:00:00

  • The in vitro interaction with DNA of several hypoxic radiosensitizers.

    abstract::The five 5-nitroimidazole derivatives and the four glyoxylic compounds tested in this paper for their interaction with DNA with and without irradiation had previously been reported to act as radiosensitizers at a cellular level. Our aim was to find if the radiosensitizing activity of these products could be due to the...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/0009-2797(89)90038-0

    authors: Santos Peinado L,Cornago Ramirez P,Lopez Zumel C

    更新日期:1989-01-01 00:00:00

  • Toxicity of Trp-P-2 to cultured human and rat keratinocytes.

    abstract::Keratinocytes cultured from human and rat epidermis exhibited strongly divergent sensitivities to toxicity from the heterocyclic amine food mutagen Trp-P-2. To find a biochemical basis for this difference, the cultured cells were compared in their expression of phase 1 and 2 biotransformation activities, mutagenic act...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/s0009-2797(00)00182-4

    authors: Chun HS,Kuzmicky PA,Kado NY,Rice RH

    更新日期:2000-07-14 00:00:00

  • Identification and characterization of reactive metabolites in myristicin-mediated mechanism-based inhibition of CYP1A2.

    abstract::Myristicin belongs to the methylenedioxyphenyl or allyl-benzene family of compounds, which are found widely in plants of the Umbelliferae family, such as parsley and carrot. Myristicin is also the major active component in the essential oils of mace and nutmeg. However, this compound can cause adverse reactions, parti...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/j.cbi.2015.06.018

    authors: Yang AH,He X,Chen JX,He LN,Jin CH,Wang LL,Zhang FL,An LJ

    更新日期:2015-07-25 00:00:00

  • Conjugation of anti-dihydrodiol epoxides of benzo[a]pyrene, chrysene, benzo[c]phenanthrene and dibenz[a,h]anthracene with glutathione catalyzed by cytosol and by the Mu-class glutathione transferase HTP II from rat liver.

    abstract::The (+/-)-anti-dihydrodiol epoxides (DE) of benzo[a]pyrene (BP), chrysene (Chr), benzo[c]phenanthrene (BcPh) and dibenz[a,h]anthracene (DBA) were incubated in the presence of glutathione (GSH) with hepatic cytosol from untreated and Aroclor 1254 pretreated rats and with the Mu-class glutathione transferase (GST) HTP I...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/0009-2797(94)03357-9

    authors: Funk M,Gath I,Seidel A,Oesch F,Platt KL

    更新日期:1995-03-30 00:00:00

  • Novel ferrocenyl pyrazoles inhibit breast cancer cell viability via induction of apoptosis and inhibition of PI3K/Akt and ERK1/2 signaling.

    abstract::Despite the advances in early detection and targeted therapies, chemotherapy is still of vital importance in breast cancer treatment. However, development of drug resistance and serious side effects limits their usage. Thus, there is an urgent need for safer and more effective agents against breast cancer. We have pre...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/j.cbi.2016.12.010

    authors: Atmaca H,Özkan AN,Zora M

    更新日期:2017-02-01 00:00:00

  • Different metabolic pathways of 2,5-difluoronitrobenzene and 2,5-difluoroaminobenzene compared to molecular orbital substrate characteristics.

    abstract::The in vivo metabolite patterns of 2,5-difluoroaminobenzene and of its nitrobenzene analogue, 2,5-difluoronitrobenzene, were determined using 19F NMR analysis of urine samples. Results obtained demonstrate significant differences between the biotransformation patterns of these two analogues. For the aminobenzene, cyto...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/0009-2797(94)03317-2

    authors: Rietjens IM,Cnubben NH,van Haandel M,Tyrakowska B,Soffers AE,Vervoort J

    更新日期:1995-01-01 00:00:00

  • The Golgi complex. III. The effects of puromycin on ultrastructure and glycoprotein synthesis.

    abstract::The effect of puromycin has been investigated on protein and glycoprotein synthesis and on ultrastructure of the Golgi complex from rat liver. Incorporation of [14C]leucine into protein in Golgi fractions and into serum proteins was depressed rapidly after puromycin treatment. In the serum proteins, incorporation retu...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/0009-2797(75)90100-3

    authors: Sturgess JM,Mitranic MM,Moscarello MA

    更新日期:1975-09-01 00:00:00

  • Drug bioactivation and protein adduct formation in the pathogenesis of drug-induced toxicity.

    abstract::Adverse drug reactions (ADRs) remain a major complication of drug therapy and can be classified as 'on-target' or 'off-target' (idiosyncratic) reactions. On-target reactions can be predicted from the known primary or secondary pharmacology of the drug and often represent an exaggeration of the pharmacological effect o...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/j.cbi.2010.09.011

    authors: Park BK,Laverty H,Srivastava A,Antoine DJ,Naisbitt D,Williams DP

    更新日期:2011-06-30 00:00:00

  • An evolutionary perspective on the first disulfide bond in members of the cholinesterase-carboxylesterase (COesterase) family: Possible outcomes for cholinesterase expression in prokaryotes.

    abstract::Within the alpha/beta hydrolase fold superfamily of proteins, the COesterase group (carboxylesterase type B, block C, cholinesterases …) diverged from the other groups through simultaneous integration of an N-terminal, first disulfide bond and a significant increase in the protein mean size. This first disulfide bond ...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/j.cbi.2019.05.016

    authors: Chatonnet A,Brazzolotto X,Hotelier T,Lenfant N,Marchot P,Bourne Y

    更新日期:2019-08-01 00:00:00

  • In vivo metabolism of nasally instilled dihydrosafrole [1-(3,4-methylenedioxyphenyl)propane] in dogs and monkeys.

    abstract::Nasal metabolism of inhaled material may influence its biological fate and toxicity. The purpose of this study was to investigate, in a noninvasive and qualitative manner, the in vivo nasal metabolic activity towards 1-(3,4-methylenedioxyphenyl)propane (dihydrosafrole). Dihydrosafrole was the compound of choice as a r...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/0009-2797(87)90056-1

    authors: Petridou-Fischer J,Whaley SL,Dahl AR

    更新日期:1987-01-01 00:00:00

  • The ability to alter the gap junction protein expression outside GST-P positive foci in liver of rats was associated to the tumour promotion potency of different polychlorinated biphenyls.

    abstract::The results demonstrate different modes of action by a dioxin-like polychlorinated biphenyl (PCB 126) and a non dioxin-like PCB (PCB 153) in the alteration of connexin (cx) 26 and cx 32 expression outside GST-P positive foci in liver of female Sprague-Dawley rats, treated according to an initiation-promotion protocol....

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/s0009-2797(97)03759-9

    authors: Bager Y,Kato Y,Kenne K,Wärngård L

    更新日期:1997-03-14 00:00:00

  • Acute dieldrin toxicity: effect on the uptake of glucose and leucine and on brush border enzymes in monkey intestine.

    abstract::Administration of a single oral dose of dieldrin (20 mg/kg body wt.) to rhesus monkeys considerably elevated the uptake of glucose and the activities of brush border sucrase, lactase, maltase and alkaline phosphatase in intestine compared to control animals. Leucine uptake and leucine amino peptidase activity was sign...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/0009-2797(81)90173-3

    authors: Mahmood A,Agarwal N,Sanyal S,Dudeja PK,Subrahmanyam D

    更新日期:1981-10-01 00:00:00