Gastroprotective activity of alkaloid extract and 2-phenylquinoline obtained from the bark of Galipea longiflora Krause (Rutaceae).

Abstract:

:As part of our continuing search for bioactive natural products from plants, the present study was carried out in order to evaluate the gastroprotective properties of alkaloid extract and 2-phenylquinoline obtained from the bark of Galipea longiflora (Rutaceae). Anti-ulcer assays were performed using the following protocols in mice: nonsteroidal anti-inflammatory drug (NSAID)/bethanecol-induced ulcer, ethanol/HCl-induced ulcer, and stress-induced ulcer. The effects of the extract on gastric content volume, pH and total acidity were also evaluated, using the pylorus ligated model. Treatment using doses of 50, 125 and 250 mg/kg of G. longiflora alkaloid extract and positive controls (omeprazol or cimetidine) significantly diminished the lesion index, total lesion area, and percentage of lesion, in comparison with the negative control groups in all the models evaluated. Regarding the model of gastric secretion, a reduction in volume of gastric juice and total acidity was observed, as well as an increase in gastric pH. The main alkaloid of the plant, 2-phenylquinoline, was also evaluated in the ethanol-induced ulcer model. The results showed that at a dose of 50 mg/kg, it significantly inhibited ulcerative lesions. However, this effect was less than that of the alkaloid extract. All these results taken together show that G. longiflora displays gastroprotective activity, as evidenced by its significant inhibition of the formation of ulcers induced by different models. There are indications that mechanisms involved in anti-ulcer activity are related to a decrease in gastric secretion and an increase in gastric mucus content. Also, there is evidence of involvement of NO in the gastroprotector mechanisms. These effects may be attributed, at least in part, to the presence of some alkaloids, particularly 2-phenylquinoline.

journal_name

Chem Biol Interact

authors

Zanatta F,Gandolfi RB,Lemos M,Ticona JC,Gimenez A,Clasen BK,Cechinel Filho V,de Andrade SF

doi

10.1016/j.cbi.2009.04.001

subject

Has Abstract

pub_date

2009-07-15 00:00:00

pages

312-7

issue

2

eissn

0009-2797

issn

1872-7786

pii

S0009-2797(09)00160-4

journal_volume

180

pub_type

杂志文章
  • Conjugation of benzo[a]pyrene metabolites by freshwater green alga Selenastrum capricornutum.

    abstract::Benzo[a]pyrene (BaP) undergoes metabolic transformation in mammals via oxidative, hydrolytic, and conjugative processes; however, little is known concerning BaP conjugation in freshwater algae. It has been shown in this laboratory that BaP is metabolized by Selenastrum capricornutum via a dioxygenase pathway. This stu...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/0009-2797(90)90061-q

    authors: Warshawsky D,Keenan TH,Reilman R,Cody TE,Radike MJ

    更新日期:1990-01-01 00:00:00

  • Identification of plasma proteins containing sulfite-reactive disulfide bonds.

    abstract::Plasma protein S-sulfonate compounds (RS-SO-3) have previously been shown to form, presumably by sulfitolysis of disulfide bonds, as a result of exposure to sulfite. In the investigations reported here, we identify two proteins in rabbit plasma, namely albumin and plasma fibronectin, which contain reactive sites for S...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/0009-2797(84)90052-8

    authors: Gregory RE,Gunnison AF

    更新日期:1984-04-01 00:00:00

  • Increased metallothionein gene expression in 5-aza-2'-deoxycytidine-induced resistance to cadmium cytotoxicity.

    abstract::The pyrimidine analog, 5-azacytidine (AZA-CR), has been shown to increase the expression of the metallothionein (MT) gene and to induce tolerance to cadmium toxicity. Since incorporation into DNA of AZA-CR appears to be required for this effect, the deoxynucleoside of AZA-CR should also be effective. Therefore, this s...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/0009-2797(88)90071-3

    authors: Waalkes MP,Miller MS,Wilson MJ,Bare RM,McDowell AE

    更新日期:1988-01-01 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

  • Suppressive effects of pelargonidin on lipopolysaccharide-induced inflammatory responses.

    abstract::Pelargonidin (PEL) is a well-known red pigment found in plants, and has been reported as having important biological activities that are potentially beneficial for human health. Here, we tested the possible use of PEL in the treatment of lipopolysaccharide (LPS)-mediated vascular inflammatory responses. The anti-infla...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/j.cbi.2019.02.007

    authors: Lee BS,Lee C,Yang S,Park EK,Ku SK,Bae JS

    更新日期:2019-04-01 00:00:00

  • Combined effect of vanadium(V) and chromium(III) on lipid peroxidation in liver and kidney of rats.

    abstract::Since chromium(III) was demonstrated to have antioxidative action, we have decided to study the effect of this element on V-induced LPO in liver and kidney of rats. Outbred 2-month-old, albino male Wistar rats received daily, for a period of 12 weeks: group I (control), deionized water to drink; group II, sodium metav...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/j.cbi.2005.11.008

    authors: Scibior A,Zaporowska H,Ostrowski J,Banach A

    更新日期:2006-02-25 00:00:00

  • Molecular cloning of neuropathy target esterase (NTE).

    abstract::Covalent modification of NTE, a neuronal protein with serine esterase activity, by certain organophosphates (OP) initiates degeneration of long axons in the peripheral and central nervous system. Simple inhibition of NTE esterase activity does not initiate neuropathy; the latter requires aging of the OP bound to the c...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章,评审

    doi:10.1016/s0009-2797(99)00065-4

    authors: Glynn P,Read DJ,Lush MJ,Li Y,Atkins J

    更新日期:1999-05-14 00:00:00

  • Chromatographic resolution of amino acid adducts of aliphatic halides.

    abstract::Numerous xenobiotics are known to be bioactivated and to covalently and to proteins, but the resulting amino acid adducts (AAAs) are unknown. In this study the AAAs of twelve 14C-labeled aliphatic halides were examined after formation in an in vitro microsomal system. After exhaustive solvent extraction of the precipi...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/0009-2797(82)90038-2

    authors: Maiorino RM,Gandolfi AJ,Brendel K,Mac Donald JR,Sipes IG

    更新日期:1982-01-01 00:00:00

  • Effect of procaine hydrochloride on DNA repair in Escherichia coli.

    abstract::Liquid-holding recovery and rejoining of gamma-radiation-induced DNA single-strand scissions in Escherichia coli could be effectively inhibited by procaine hydrochloride at the concentration of 20 mM. At this concentration, the drug also reversibly altered cellular permeability barrier as evidenced from the uptake of ...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/0009-2797(75)90097-6

    authors: Nair CK,Pradhan DS

    更新日期:1975-09-01 00:00:00

  • Impact of exogenous lysolipids on sensitive and multidrug resistant K562 cells: 1H NMR studies.

    abstract::The ability of lysolipids to enter into a membrane bi-layer and disturb the membrane structure was used to study the behavior of K562 erythroleukemic cells, K562 wild type (K562wt) as well as the multidrug resistant cells K562adr. Both types of cells, when analyzed by proton NMR spectroscopy exhibit the high resolutio...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/j.cbi.2004.12.005

    authors: Traïkia M,Marbeuf-Gueye C,Hantz E,Le Moyec L

    更新日期:2005-01-15 00:00:00

  • Salidroside attenuates colistin-induced neurotoxicity in RSC96 Schwann cells through PI3K/Akt pathway.

    abstract::Neurotoxicity is a key dose-limiting factor for colistin therapy. This study aimed to investigate the protective effect of Salidroside on colistin-induced neurotoxicity in RSC96 Schwann cells and the underlying mechanisms. After Salidroside (12.5, 25, 50 μg/mL) treatment for 2 h, the cells were cultured with 250 μg/mL...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/j.cbi.2017.04.027

    authors: Lu Z,Jiang G,Chen Y,Wang J,Muhammad I,Zhang L,Wang R,Liu F,Li R,Qian F,Li J

    更新日期:2017-06-01 00:00:00

  • Inhibition of CYP1A1 enzyme activity in mouse hepatoma cell culture by soybean isoflavones.

    abstract::The mechanisms by which soybean- and soybean isoflavone-enriched diets inhibit carcinogenesis are not known. We found that the isoflavones genistin and daidzin, and their respective aglucone forms daidzein and genistein, block 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD; dioxin)-induced CYP1A1 enzyme activity. This inhi...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/s0009-2797(99)00121-0

    authors: Shertzer HG,Puga A,Chang C,Smith P,Nebert DW,Setchell KD,Dalton TP

    更新日期:1999-11-15 00:00:00

  • 6-Shogaol enhances renal carcinoma Caki cells to TRAIL-induced apoptosis through reactive oxygen species-mediated cytochrome c release and down-regulation of c-FLIP(L) expression.

    abstract::6-Shogaol, a potent bioactive compound in ginger (Zingiber officinale Roscoe), has been reported for anti-inflammatory and anti-cancer activity. In this study, we investigated the effect of 6-shogaol to enhance tumor necrosis factor-related apoptosis-inducing ligand (TRAIL)-mediated apoptosis. The combined treatment w...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/j.cbi.2015.01.020

    authors: Han MA,Woo SM,Min KJ,Kim S,Park JW,Kim DE,Kim SH,Choi YH,Kwon TK

    更新日期:2015-02-25 00:00:00

  • Mechanism of bioactivation and covalent binding of 2,4,6-trinitrotoluene.

    abstract::Studies were undertaken to investigate the mechanism of bioactivation and covalent binding of TNT. Incubation of [14C]TNT with rat liver microsomes in the presence of an NADPH generating system resulted in metabolism and covalent binding to microsomal proteins. Time-dependence studies showed that TNT was rapidly reduc...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/0009-2797(94)03606-9

    authors: Leung KH,Yao M,Stearns R,Chiu SH

    更新日期:1995-06-30 00:00:00

  • Comparison of pharmacokinetic and pharmacodynamic profiles of aspirin following oral gavage and diet dosing in rats.

    abstract::Aspirin is one of the oldest drugs and has been purported to have multiple beneficial effects, including prevention of cardiovascular disease and cancer, in addition to its original indication for treatment of inflammation, fever and pain. In cancer chemoprevention studies using animal models, two methods of aspirin a...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/j.cbi.2008.10.008

    authors: Kapetanovic IM,Bauer KS,Tessier DM,Lindeblad MO,Zakharov AD,Lubet R,Lyubimov A

    更新日期:2009-05-15 00:00:00

  • Tissue oxidative damage mediates impairment on phosphotransfer network during thymol intake: Effects on hepatic and renal bioenergetics.

    abstract::Recent evidences demonstrated that ingestion of several monoterpenes cause hepatic and renal damage due to impairment on mitochondrial energy production, eliciting a collapse on adenosine triphosphate (ATP) synthesis and consequently impairment on bioenergetic homeostasis. Thus, the aim of this study was to evaluate w...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/j.cbi.2018.09.009

    authors: Baldissera MD,Souza CF,De Matos AFIM,Baldisserotto B,da Silva AS,Monteiro SG

    更新日期:2018-12-25 00:00:00

  • Differential inhibition of hepatic microsomal alkoxyresorufin O-dealkylation activities by tetrachlorobiphenyls.

    abstract::Polychlorinated biphenyls (PCBs) elicit a spectrum of biochemical and toxic effects in exposed animals. In the present study, we assessed the effect of PCB structure, using four symmetrically-substituted PCBs, on cytochrome P450 (CYP)-mediated methoxy-, ethoxy- and benzyloxyresorufin O-dealkylase (MROD, EROD and BROD,...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/j.cbi.2007.05.004

    authors: Edwards PR,Hrycay EG,Bandiera SM

    更新日期:2007-08-15 00:00:00

  • N-methyl-4-phenylpyridinium (MPP+) potentiates the killing of cultured hepatocytes by catecholamines.

    abstract::The role of catecholamines in the toxicity of MPTP (N-methyl-4-phenyl- 1,2,3,6-tetrahydropyridine) was explored. The killing of cultured hepatocytes by dopamine and 6-hydroxydopamine was enhanced following inhibition of glutathione reductase by 1,3-bis(2-chloroethyl)-1-nitrosourea (BCNU), a manipulation known to sensi...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/0009-2797(93)90092-d

    authors: Snyder JW,Alexander GM,Ferraro TN,Grothusen JR,Farber JL

    更新日期:1993-09-01 00:00:00

  • Pulmonary delivery of an aerosolized recombinant human butyrylcholinesterase pretreatment protects against aerosolized paraoxon in macaques.

    abstract::Butyrylcholinesterase (BChE) is the leading pretreatment candidate against exposure to organophosphates (OPs), which pose an ever increasing public and military health. Since respiratory failure is the primary cause of death following acute OP poisoning, an inhaled BChE therapeutic could prove highly efficacious in pr...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/j.cbi.2012.11.004

    authors: Rosenberg YJ,Laube B,Mao L,Jiang X,Hernandez-Abanto S,Lee KD,Adams R

    更新日期:2013-03-25 00:00:00

  • Mitochondrial involvement in genetically determined transition metal toxicity II. Copper toxicity.

    abstract::Copper, like iron, is an essential transition metal ion in which its redox reactivity, whilst essential for the activity of mitochondrial enzymes, can also be a source of harmful reactive oxygen species if not chelated to biomolecules. Therefore, both metals are sequestered by protein chaperones and moved across membr...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章,评审

    doi:10.1016/j.cbi.2006.05.011

    authors: Mehta R,Templeton DM,O'brien PJ

    更新日期:2006-10-27 00:00:00

  • Template properties of DNA alkylated with N-methyl-N-nitrosourea and N-ethyl-N-nitrosourea.

    abstract::Alkylation of DNA with N-methyl-N-nitrosourea (MeNU) and N-ethyl-N-nitrosourea (EtNU) reduces its ability to support RNA synthesis catalyzed by exogenously added RNA polymerase. It is likely that 7-alkylguanine and alkyl phosphotriester in DNA are mainly responsible for the inhibition of RNA synthesis. The inhibitory ...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/0009-2797(83)90027-3

    authors: Marushige K,Marushige Y

    更新日期:1983-09-01 00:00:00

  • The lysosomal-mitochondrial axis theory of postmitotic aging and cell death.

    abstract::Aging (senescence) is characterized by a progressive accumulation of macromolecular damage, supposedly due to a continuous minor oxidative stress associated with mitochondrial respiration. Aging mainly affects long-lived postmitotic cells, such as neurons and cardiac myocytes, which neither divide and dilute damaged s...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章,评审

    doi:10.1016/j.cbi.2006.04.013

    authors: Terman A,Gustafsson B,Brunk UT

    更新日期:2006-10-27 00:00:00

  • Inhibition of human prostatic tumour acid phosphatase by N,N-p-di-2-chloroethylaminophenol, N,N-p-di-2-chloroethylaminophenyl phosphate and other difunctional nitrogen mustards.

    abstract::Potent inhibition of human prostatic carcinoma tissue acid phosphatase by N,N-d-di-2-chloroethylaminophenol (AMOH) and N,N-p-di-2-chloroethylaminophenyl phosphate (AMPh) is described. Certain other difunctional nitrogen mustards were also inhibitory but N,N-p-di-2hydroxyethylaminophenol, the non-alkylating fully hydro...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/0009-2797(78)90085-6

    authors: Workman P

    更新日期:1978-01-01 00:00:00

  • Short-chain dehydrogenases/reductases (SDR): the 2002 update.

    abstract::Short-chain dehydrogenases/reductases (SDR) form a large, functionally heterogeneous protein family presently with about 3000 primary and about 30 3D structures deposited in databases. Despite low sequence identities between different forms (about 15-30%), the 3D structures display highly similar alpha/beta folding pa...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章,评审

    doi:10.1016/s0009-2797(02)00164-3

    authors: Oppermann U,Filling C,Hult M,Shafqat N,Wu X,Lindh M,Shafqat J,Nordling E,Kallberg Y,Persson B,Jörnvall H

    更新日期:2003-02-01 00:00:00

  • Avermectin induces P-glycoprotein expression in S2 cells via the calcium/calmodulin/NF-κB pathway.

    abstract::Avermectin (AVM) is a macrocyclic lactone agent widely used as a nematicide, acaricide and insecticide in veterinary medicine and plant protection. P-glycoprotein (P-gp) is an ATP-dependent drug efflux pump for xenobiotic compounds, and is involved in multidrug resistance. To understand the development of AVM resistan...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/j.cbi.2013.03.009

    authors: Luo L,Sun YJ,Yang L,Huang S,Wu YJ

    更新日期:2013-04-25 00:00:00

  • Potential for selective modulation of glutathione in cancer chemotherapy.

    abstract::Notwithstanding ongoing progress in anticancer therapeutics development, the persistent problem remains to selectively target tumors while sparing normal tissues. This is confounding largely because the differences between normal and tumor cells are often subtle and part of a gradient, where a gene product may be more...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章,评审

    doi:10.1016/s0009-2797(97)00166-x

    authors: Chen X,Carystinos GD,Batist G

    更新日期:1998-04-24 00:00:00

  • Effects of benzo(a)pyrene adducts of DNA synthesis in vitro.

    abstract::Two diol epoxides of benzo(a)pyrene (BP), and benzo(a)pyrene 4,5-oxide, have been used to make adducts in the homopolymers polyribocytidylic acid, (rC); polyriboadenylic acid (rA), polydeoxycytidylic acid (dC) and polydeoxyadenylic acid (dA). With appropriate oligomers as primers these modified and unmodified polynucl...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/0009-2797(78)90100-x

    authors: Yamaura I,Marquardt H,Cavalieri LF

    更新日期:1978-12-01 00:00:00

  • Paraoxonases, mitochondrial dysfunction and non-communicable diseases.

    abstract::The most common non-communicable diseases (NCD) are obesity, cardiovascular disease, diabetes, cancer, chronic respiratory diseases, and neurological diseases. Together, they constitute the commonest cause of death and disability worldwide. Mitochondrial alterations, oxidative stress and inflammation underpin NCD and ...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章,评审

    doi:10.1016/j.cbi.2016.04.005

    authors: Camps J,García-Heredia A,Hernández-Aguilera A,Joven J

    更新日期:2016-11-25 00:00:00

  • Putting bioactivation reactions to work: Targeting antioxidants to mitochondria.

    abstract::The goal of this research was to test the hypothesis that bioactivation reactions could be exploited to deliver and activate mitochondria-targeted antioxidant prodrugs. The concept that bioactivation reactions could be used for prodrug delivery and activation has received little attention. Most bioactivation reactions...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章,评审

    doi:10.1016/j.cbi.2010.10.004

    authors: Anders MW

    更新日期:2011-06-30 00:00:00

  • Accumulation and elimination of macromolecular lesions in susceptible and non-susceptible rat tissues after repeated administration of trans-4-acetylaminostilbene.

    abstract::Trans-4-acetylaminostilbene (trans-AAS) is a potent carcinogen and quite specifically produces sebaceous gland tumors, predominantly in the Zymbal's gland of rats. It is also acutely toxic to the rat glandular stomach. Recent results have shown that these target tissues are not notably exposed to reactive metabolites ...

    journal_title:Chemico-biological interactions

    pub_type: 杂志文章

    doi:10.1016/s0009-2797(85)80154-x

    authors: Hilpert D,Neumann HG

    更新日期:1985-06-01 00:00:00