Effects of cardio-pulmonary bypass on vancomycin plasma concentration decay.

Abstract:

:The objective of the study was to investigate possible changes in vancomycin serum levels induced by cardio-pulmonary bypass (CPB). Ten cardiac patients (seven males, three females, aged between 56 and 81), who underwent cardiac surgery requiring CPB, took part in the study. Vancomycin (15 mg kg-1) was intravenously infused over 60 min before anaesthesia and blood samples were taken at appropriate times after drug administration (0, 0.5, 1, 6, 8 h), after starting CPB (0, 5, 30 and 60 min) and after aortic unclamping (0, 5, 30, 60, 120 min). Drug serum concentrations were determined by means of a fluorescence polarization immunoassay. The area under the concentration-time curve (AUC) measured during CPB were compared with the AUC extrapolated in the same interval by fitting a two-compartment pharmacokinetic model to drug concentrations obtained before and after CPB. Five minutes after starting CPB vancomycin serum levels decreased, on average, by 40.9% and remained steadily lower than the expected values over the next 60 min. In the same interval, the measured AUC was 31.7% lower than the expected AUC. In no instance did serum levels fall below the MIC for most common pathogens (1-2 mg l-1). At aortic unclamping serum levels slightly rebounded but tended to remain lower than the expected concentrations over the next 120 min. In conclusion, during CPB vancomycin serum levels invariably decreased but, at the dose employed (15 mg kg-1), remained in a potentially effective range for antimicrobial prophylaxis.

journal_name

Pharmacol Res

journal_title

Pharmacological research

authors

Miglioli PA,Merlo F,Grabocka E,Padrini R

doi

10.1006/phrs.1998.0370

subject

Has Abstract

pub_date

1998-10-01 00:00:00

pages

275-8

issue

4

eissn

1043-6618

issn

1096-1186

pii

S1043-6618(98)90370-X

journal_volume

38

pub_type

临床试验,杂志文章
  • Cinnamtannin D1 attenuates autoimmune arthritis by regulating the balance of Th17 and treg cells through inhibition of aryl hydrocarbon receptor expression.

    abstract::The suppression of the abnormal systemic immune response constitutes a primary strategy for treatment of rheumatoid arthritis (RA); toward this end, the identification of natural compounds with immunosuppressive activity represents a promising strategy for RA drug discovery. Cinnamtannin D1 (CTD-1), a polyphenolic com...

    journal_title:Pharmacological research

    pub_type: 杂志文章

    doi:10.1016/j.phrs.2019.104513

    authors: Shi C,Zhang H,Wang X,Jin B,Jia Q,Li Y,Yang Y

    更新日期:2020-01-01 00:00:00

  • Loganin possesses neuroprotective properties, restores SMN protein and activates protein synthesis positive regulator Akt/mTOR in experimental models of spinal muscular atrophy.

    abstract::Spinal muscular atrophy (SMA) is an autosomal recessive neurodegenerative disease characterized by motor neurons degeneration and muscular atrophy. There is no effective SMA treatment. Loganin is a botanical candidate with anti-inflammatory, anti-oxidant, glucose-lowering and anti-diabetic nephropathy activities. The ...

    journal_title:Pharmacological research

    pub_type: 杂志文章

    doi:10.1016/j.phrs.2016.05.023

    authors: Tseng YT,Chen CS,Jong YJ,Chang FR,Lo YC

    更新日期:2016-09-01 00:00:00

  • Immunological regulatory effect of flavonoid baicalin on innate immune toll-like receptors.

    abstract::As an essential component of the innate immune system, Toll-like receptors (TLRs) are a family of well-recognized ligand-binding receptors found in various organisms and initiate host immune responses. Activation of TLRs signaling pathways lead to the induction of numerous genes that function in host defense. Baicalin...

    journal_title:Pharmacological research

    pub_type: 杂志文章,评审

    doi:10.1016/j.phrs.2020.104890

    authors: Jiang M,Li Z,Zhu G

    更新日期:2020-08-01 00:00:00

  • Fostering efficacy and toxicity evaluation of traditional Chinese medicine and natural products: Chick embryo as a high throughput model bridging in vitro and in vivo studies.

    abstract::Efficacy and safety assessments are essential thresholds for drug candidates from preclinical to clinical research. Conventional mammalian in vivo models cannot offer rapid pharmacological and toxicological screening, whereas cell-based or cell-free in vitro systems often lead to inaccurate results because of the lack...

    journal_title:Pharmacological research

    pub_type: 杂志文章,评审

    doi:10.1016/j.phrs.2018.04.011

    authors: Wu T,Yu GY,Xiao J,Yan C,Kurihara H,Li YF,So KF,He RR

    更新日期:2018-07-01 00:00:00

  • ATB-346, a novel hydrogen sulfide-releasing anti-inflammatory drug, induces apoptosis of human melanoma cells and inhibits melanoma development in vivo.

    abstract::Inflammation plays a key role in tumor promotion and development. Indeed, cyclooxygenase-2 (COX-2) expression is strongly associated with different types of cancer. An emerging class of compounds with significant anti-inflammatory properties is the hydrogen sulfide-releasing non-steroidal anti-inflammatory drugs (H2S-...

    journal_title:Pharmacological research

    pub_type: 杂志文章

    doi:10.1016/j.phrs.2016.10.019

    authors: De Cicco P,Panza E,Ercolano G,Armogida C,Sessa G,Pirozzi G,Cirino G,Wallace JL,Ianaro A

    更新日期:2016-12-01 00:00:00

  • Mfsd2a-based pharmacological strategies for drug delivery across the blood-brain barrier.

    abstract::The blood-brain barrier (BBB) keeps the central nervous system (CNS) safe from various brain diseases, while the BBB makes it difficult for effective drugs to enter the CNS. Mfsd2a is specifically expressed on the cell membrane of brain-microvascular endothelial cell (BMEC) and is implicated in the delivery of some su...

    journal_title:Pharmacological research

    pub_type: 杂志文章

    doi:10.1016/j.phrs.2015.12.024

    authors: Wang JZ,Xiao N,Zhang YZ,Zhao CX,Guo XH,Lu LM

    更新日期:2016-02-01 00:00:00

  • Gene silencing of receptor-interacting protein 2 protects against cigarette smoke-induced acute lung injury.

    abstract:BACKGROUND AND PURPOSE:Chronic obstructive pulmonary disease (COPD) is characterized by progressive alveolar damage and generally irreversible airflow limitation. Nuclear factor-κB (NF-κB) plays a critical role in COPD pathogenesis. Receptor-interacting protein 2 (Rip2), a 60 kDa adaptor protein, is a positive regulato...

    journal_title:Pharmacological research

    pub_type: 杂志文章

    doi:10.1016/j.phrs.2018.10.016

    authors: Dong J,Liao W,Tan LH,Yong A,Peh WY,Wong WSF

    更新日期:2019-01-01 00:00:00

  • Gas chromatographic assay for estazolam in human plasma and results of a bioequivalence study.

    abstract::This paper describes a new sensitive gas chromatographic method with electron capture detector to assay estazolam in human plasma, which has been developed and validated for pharmacokinetic purposes. The drug and the internal standard (triazolam) were extracted from plasma buffered at pH 9.0 into toluene and analysed ...

    journal_title:Pharmacological research

    pub_type: 临床试验,杂志文章,随机对照试验

    doi:10.1006/phrs.1997.0144

    authors: Dal Bo L,Verga F,Marzo A,La Commare P,De Vito ML

    更新日期:1997-04-01 00:00:00

  • Effects of acetylbergenin against D -galactosamine-induced hepatotoxicity in rats.

    abstract::The hepatoprotective effects of acetylbergenin were examined against D -galactosamine (GalN)-induced liver damage in rats, compared with that of bergenin reported previously. Acetylbergenin was synthesized from acetylation of bergenin, isolated from Mallotus japonicus, to increase lipophilic and physiological activiti...

    journal_title:Pharmacological research

    pub_type: 杂志文章

    doi:10.1006/phrs.2000.0730

    authors: Lim HK,Kim HS,Choi HS,Oh S,Jang CG,Choi J,Kim SH,Chang MJ

    更新日期:2000-11-01 00:00:00

  • Statins in chronic kidney disease and kidney transplantation.

    abstract::HMG-CoA reductase inhibitors (statins) have been shown to improve cardiovascular (CV) outcomes in the general population as well as in patients with cardiovascular disease (CVD). Statins' beneficial effects have been attributed to both cholesterol-lowering and cholesterol-independent "pleiotropic" properties. By their...

    journal_title:Pharmacological research

    pub_type: 杂志文章,评审

    doi:10.1016/j.phrs.2014.06.011

    authors: Kassimatis TI,Goldsmith DJ

    更新日期:2014-10-01 00:00:00

  • Antiplatelet and antithrombotic activities of essential oil from wild Ocotea quixos (Lam.) Kosterm. (Lauraceae) calices from Amazonian Ecuador.

    abstract::Ocotea quixos essential oil was shown to possess significant inhibitory activity of platelet aggregation and clot retraction in rodent plasma. This study is aimed at fully characterizing the antiplatelet activity of the whole essential oil and its main components trans-cinnamaldehyde and methyl cinnamate also in human...

    journal_title:Pharmacological research

    pub_type: 杂志文章

    doi:10.1016/j.phrs.2006.09.009

    authors: Ballabeni V,Tognolini M,Bertoni S,Bruni R,Guerrini A,Rueda GM,Barocelli E

    更新日期:2007-01-01 00:00:00

  • Thymidylate synthase expression and genotype have no major impact on the clinical outcome of colorectal cancer patients treated with 5-fluorouracil.

    abstract:BACKGROUND AND OBJECTIVES:Thymidylate synthase (TS) expression levels appear to be related to response to 5-fluorouracil-(5-FU)-based chemotherapy in colorectal cancer (CRC) patients. Three polymorphisms have been proposed as modulators of TS expression: a tandemly repeated sequence (2R/3R) in the 5' UTR, a SNP (G>C) w...

    journal_title:Pharmacological research

    pub_type: 杂志文章

    doi:10.1016/j.phrs.2011.04.006

    authors: Vignoli M,Nobili S,Napoli C,Putignano AL,Morganti M,Papi L,Valanzano R,Cianchi F,Tonelli F,Mazzei T,Mini E,Genuardi M

    更新日期:2011-09-01 00:00:00

  • The rise and fall of compartmental analysis.

    abstract::The concept of compartment evolved in the contexts of radioactivity, physiology, pharmacology and tracer kinetics. Recently compartmental models have been compared with 'physiological models', even though in most cases the same, or stricter hypotheses, are necessary for the validity of these latter models. This paper ...

    journal_title:Pharmacological research

    pub_type: 杂志文章

    doi:10.1006/phrs.2001.0873

    authors: Rescigno A

    更新日期:2001-10-01 00:00:00

  • Poly(ADP-ribosyl)ation and stroke.

    abstract::Over the past decade, poly(ADP-ribosyl)ation has emerged as a crucial event in the pathogenesis of ischemic stroke. A large body of evidence unambiguously demonstrates that activity of poly(ADP-ribose) polymerase-1 (PARP-1) significantly increases during brain ischemia, and that inhibition of this enzymatic activity a...

    journal_title:Pharmacological research

    pub_type: 杂志文章,评审

    doi:10.1016/j.phrs.2005.02.018

    authors: Chiarugi A

    更新日期:2005-07-01 00:00:00

  • Antisense oligonucleotides as therapeutic agents.

    abstract::The potential for modulating gene expression by the use of antisense oligonucleotides has become increasingly interesting in recent years. Antisense oligonucleotides are complementary nucleic acid fragments that hybridize to target sequences within RNA to form a DNA-RNA duplex, resulting in the block of translation of...

    journal_title:Pharmacological research

    pub_type: 杂志文章,评审

    doi:10.1006/phrs.1997.0227

    authors: Alama A,Barbieri F,Cagnoli M,Schettini G

    更新日期:1997-09-01 00:00:00

  • Pharmacological chaperone approaches for rescuing GPCR mutants: Current state, challenges, and screening strategies.

    abstract::A substantial number of G-protein coupled receptors (GPCRs) genetic disorders are due to mutations that cause misfolding or dysfunction of the receptor product. Pharmacological chaperoning approaches can rescue such mutant receptors by stabilizing protein conformations that behave similar to the wild type protein. For...

    journal_title:Pharmacological research

    pub_type: 杂志文章,评审

    doi:10.1016/j.phrs.2016.12.036

    authors: Beerepoot P,Nazari R,Salahpour A

    更新日期:2017-03-01 00:00:00

  • Viral G protein-coupled receptors as modulators of cancer hallmarks.

    abstract::Herpesviruses encode transmembrane G protein-coupled receptors (GPCRs), which share structural homology to human chemokine receptors. These viral GPCRs include KSHV-encoded ORF74, EBV-encoded BILF1, and HCMV-encoded US28, UL33, UL78 and US27. Viral GPCRs hijack various signaling pathways and cellular networks, includi...

    journal_title:Pharmacological research

    pub_type: 杂志文章,评审

    doi:10.1016/j.phrs.2020.104804

    authors: van Senten JR,Fan TS,Siderius M,Smit MJ

    更新日期:2020-06-01 00:00:00

  • Raloxifene inhibits matrix metalloproteinases expression and activity in macrophages and smooth muscle cells.

    abstract::Secretion of matrix metalloproteinases (MMPs) by macrophages and smooth muscle cells (SMC) may impair atherosclerotic cap integrity leading to atherosclerosis complications. Selective estrogen receptor modulators (SERMs) have favourable impact on plasma lipid levels, but their role in the prevention of atherosclerosis...

    journal_title:Pharmacological research

    pub_type: 杂志文章

    doi:10.1016/j.phrs.2007.05.004

    authors: Bellosta S,Baetta R,Canavesi M,Comparato C,Granata A,Monetti M,Cairoli F,Eberini I,Puglisi L,Corsini A

    更新日期:2007-08-01 00:00:00

  • Dopaminergic projection to the septum mediates facilitatory effect of angiotensins on recognition memory in rats.

    abstract::We have previously reported that the dopaminergic projection from A10 ventral tegmental neurons to the central amygdala is, in part, responsible for the facilitatory effect of angiotensin II (AII) and its 3-7 fragment [AII(3-7)] on the retrieval of information in memory motivated affectively and also on recognition me...

    journal_title:Pharmacological research

    pub_type: 杂志文章

    doi:10.1006/phrs.1997.0257

    authors: Winnicka MM,Braszko JJ,Wiśniewski K

    更新日期:1997-11-01 00:00:00

  • The non-NMDA receptor antagonist NBQX does not affect rats performance in the object recognition task.

    abstract::Though the AMPA receptor has been implicated in several neurodegenerative processes (epilepsy, ischemia, spasticity), its role in cognition is yet to be clarified. The aim of this study was to assess in the rat the effects of the AMPA receptor antagonist NBQX (3.5, 7, 10, 20 and 30 mgkg(-1), i.p.) on learning and memo...

    journal_title:Pharmacological research

    pub_type: 杂志文章

    doi:10.1006/phrs.2001.0898

    authors: Pitsikas N,Rigamonti AE,Cella SG,Muller EE

    更新日期:2002-01-01 00:00:00

  • Effect of captopril on doxorubicin-induced nephrotoxicity in normal rats.

    abstract::Biochemical evaluations of the effects of the sulfhydryl-containing angiotensin-converting enzyme inhibitor (captopril) on the nephrotoxicity induced by doxorubicin in normal rats were carried out. A single dose of doxorubicin (15 mg kg-1) which caused nephrotoxicity was manifested biochemically by the elevation of se...

    journal_title:Pharmacological research

    pub_type: 杂志文章

    doi:10.1006/phrs.1998.0432

    authors: Mansour MA,El-Kashef HA,Al-Shabanah OA

    更新日期:1999-03-01 00:00:00

  • Modification of reserpine-induced emetic response in pigeons by alpha 2-adrenoceptors.

    abstract::In the present study, an attempt has been made to elucidate the role of alpha 2-adrenoceptors in reserpine-induced emesis in pigeons. Reserpine was found to induce dose-dependent emesis and a 500 micrograms kg-1 dose was found to be the 100% emetic dose. alpha 2-adrenoceptor agonists clonidine and alpha-methylnoradren...

    journal_title:Pharmacological research

    pub_type: 杂志文章

    doi:10.1016/1043-6618(94)80060-x

    authors: Khandker SK,Mukerjee D,Gurtu S,Pant KK,Dhawan KN,Sinha JN

    更新日期:1994-05-01 00:00:00

  • Lupeol and its derivatives as anticancer and anti-inflammatory agents: Molecular mechanisms and therapeutic efficacy.

    abstract::Lupeol is a natural triterpenoid that widely exists in edible fruits and vegetables, and medicinal plants. In the last decade, a plethora of studies on the pharmacological activities of lupeol have been conducted and have demonstrated that lupeol possesses an extensive range of pharmacological activities such as antic...

    journal_title:Pharmacological research

    pub_type: 杂志文章,评审

    doi:10.1016/j.phrs.2020.105373

    authors: Liu K,Zhang X,Xie L,Deng M,Chen H,Song J,Long J,Li X,Luo J

    更新日期:2020-12-11 00:00:00

  • Involvement of the GABAA receptor α subunit in the mode of action of etifoxine.

    abstract::Etifoxine (EFX) is a non-benzodiazepine psychoactive drug which exhibits anxiolytic effects through a dual mechanism, by directly binding to GABAA receptors (GABAARs) and to the mitochondrial 18-kDa translocator protein, resulting in the potentiation of the GABAergic function. The β subunit subtype plays a key role in...

    journal_title:Pharmacological research

    pub_type: 杂志文章

    doi:10.1016/j.phrs.2019.04.034

    authors: Mattei C,Taly A,Soualah Z,Saulais O,Henrion D,Guérineau NC,Verleye M,Legros C

    更新日期:2019-07-01 00:00:00

  • Relationship between constitutive nitric oxide synthase activity and mucus level in the gastric mucosa of rats with stress.

    abstract::A decrease in constitutive nitric oxide synthase (cNOS) activity occurred with decreases in hexosamine (an index of mucus synthesis) and adherent mucus (an index of mucus secretion) concentrations in the gastric mucosa of rats with water immersion restraint (WIR) stress. The decreases in gastric mucosal hexosamine and...

    journal_title:Pharmacological research

    pub_type: 杂志文章

    doi:10.1006/phrs.1998.0379

    authors: Nishida K,Ohta Y,Ishiguro I

    更新日期:1998-11-01 00:00:00

  • TRPM8 channel activation triggers relaxation of pudendal artery with increased sensitivity in the hypertensive rats.

    abstract:INTRODUCTION:Erectile dysfunction (ED) is frequently encountered in patients with arterial hypertension and there is a recent functional correlation between the expression of thermoreceptor channels TRPM8 (melastatin 8) and alterations in blood pressure in hypertension. The aim of this study was to investigate the func...

    journal_title:Pharmacological research

    pub_type: 杂志文章

    doi:10.1016/j.phrs.2019.104329

    authors: Silva DF,Wenceslau CF,Mccarthy CG,Szasz T,Ogbi S,Webb RC

    更新日期:2019-09-01 00:00:00

  • Etrolizumab versus infliximab in the treatment of induction phase of ulcerative colitis: A systematic review and indirect comparison.

    abstract:OBJECTIVES:There is still a need to develop new effective medications for the treatment of ulcerative colitis, particularly for patients who are intolerant or resistant to first line therapies. This article compared the efficacy and safety of etrolizumab and infliximab in moderate to severe ulcerative colitis. METHODS...

    journal_title:Pharmacological research

    pub_type: 杂志文章,meta分析

    doi:10.1016/j.phrs.2018.11.003

    authors: Motaghi E,Ghasemi-Pirbaluti M,Zabihi M

    更新日期:2019-01-01 00:00:00

  • From stroke to neurodegenerative diseases: The multi-target neuroprotective effects of 3-n-butylphthalide and its derivatives.

    abstract::Discovering effective agents to slow or stop neurodegeneration is a challenging task. Over decades, only a few drugs were approved by Food and Drug Administration (FDA) and most ended in failure. The lessons learned have switched the strategy of drug discovery from designing highly selective ligands to a network pharm...

    journal_title:Pharmacological research

    pub_type: 杂志文章,评审

    doi:10.1016/j.phrs.2018.08.007

    authors: Huang L,Wang S,Ma F,Zhang Y,Peng Y,Xing C,Feng Y,Wang X,Peng Y

    更新日期:2018-09-01 00:00:00

  • Anti-platelet activity of KR-32560, a novel sodium/hydrogen exchanger-1 inhibitor.

    abstract::We investigated the anti-platelet effect of a newly synthesized guanidine derivative KR-32560, a sodium/hydrogen exchanger-1 (NHE-1) inhibitor, together with the elucidation of the possible mode of action. KR-32560 concentration dependently inhibited the aggregation of washed rabbit platelets induced by collagen (10 m...

    journal_title:Pharmacological research

    pub_type: 杂志文章

    doi:10.1016/j.phrs.2005.12.003

    authors: Lee KS,Jin YR,Lee JJ,Lim Y,Son DJ,Lee CK,Yi KY,Yoo SE,Shin HS,Yun YP

    更新日期:2006-03-01 00:00:00

  • Electrophysiological and metabolic effects of CHF5074 in the hippocampus: protection against in vitro ischemia.

    abstract::CHF5074 is a non-steroidal anti-inflammatory derivative holding disease-modifying potential for the treatment of Alzheimer's disease. The aim of the present study was to characterize the electrophysiological and metabolic profile of CHF5074 in the hippocampus. Electrophysiological recordings show that CHF5074 inhibits...

    journal_title:Pharmacological research

    pub_type: 杂志文章

    doi:10.1016/j.phrs.2014.02.010

    authors: Mango D,Barbato G,Piccirilli S,Panico MB,Feligioni M,Schepisi C,Graziani M,Porrini V,Benarese M,Lanzillotta A,Pizzi M,Pieraccini S,Sironi M,Blandini F,Nicoletti F,Mercuri NB,Imbimbo BP,Nisticò R

    更新日期:2014-03-01 00:00:00