Polyfluorinated alkyl phosphate ester surfactants - current knowledge and knowledge gaps.

Abstract:

:Fluorochemicals are a diverse group of synthetically produced compounds with the unique ability to repel water as well as oil. This property makes them ideal for multiple purposes in a variety of consumer and industrial products. Fluorochemicals have been detected in the environment, as well as in human blood, urine and milk. Due to their long half-life in human beings, there is an increased risk that exposure to these compounds can cause adverse effects. However, except for perfluorooctanoic acid (PFOA) and perfluorooctanesulfonic acid (PFOS), there is a large data gap regarding toxicological information on fluorochemicals. Polyfluorinated alkyl phosphate ester surfactants (PAPs) belong to the group of polyfluorinated alkyl surfactants. They have been detected in indoor dust and are widely used in food-contact materials, from which they have the ability to migrate into food. Toxicological data on PAPs are very limited, but current studies indicate that some PAPs have the potential to interfere with sex hormone synthesis in vitro. Disturbance of the sex hormone balance in foetal life has been suggested to be an important mechanism involved in adverse effects on, for example, male reproductive health and development. The current lack of toxicological data on PAPs impairs the risk assessment of this group of compounds. However, until more toxicological data on PAPs are available, the limited data currently accessible give reason to believe that these compounds might have the ability to cause potentially adverse effects, as seen for other perfluorinated chemicals, including some metabolic products of PAPs.

authors

Taxvig C,Rosenmai AK,Vinggaard AM

doi

10.1111/bcpt.12208

subject

Has Abstract

pub_date

2014-07-01 00:00:00

pages

41-4

issue

1

eissn

1742-7835

issn

1742-7843

journal_volume

115

pub_type

杂志文章,评审
  • A novel COX-2 inhibitor pyrazole derivative proven effective as an anti-inflammatory and analgesic drug.

    abstract::The introduction of new COX-2 inhibitors with high efficacy and enhanced safety profile would be a great achievement in the development of anti-inflammatory drugs. This study was designed to screen and assess the anti-inflammatory and analgesic activities as well as some of the expected side effects of some pyrazole d...

    journal_title:Basic & clinical pharmacology & toxicology

    pub_type: 杂志文章

    doi:10.1111/j.1742-7843.2010.00648.x

    authors: Mohy El-Din MM,Senbel AM,Bistawroos AA,El-Mallah A,Nour El-Din NA,Bekhit AA,Abd El Razik HA

    更新日期:2011-04-01 00:00:00

  • Wuzhi capsule regulates chloroacetaldehyde pharmacokinetics behaviour and alleviates high-dose cyclophosphamide-induced nephrotoxicity and neurotoxicity in rats.

    abstract::High-dose cyclophosphamide (HD-CTX) treatment often leads to severe nephrotoxicity and neurotoxicity, which are mainly caused by one of its metabolites, chloroacetaldehyde (CAA). However, there are no effective antidotes to prevent these side effects. The objective of this study was to evaluate the effect of Wuzhi Cap...

    journal_title:Basic & clinical pharmacology & toxicology

    pub_type: 杂志文章

    doi:10.1111/bcpt.13211

    authors: Chen L,Xiong X,Hou X,Wei H,Zhai J,Xia T,Gong X,Gao S,Feng G,Tao X,Zhang F,Chen W

    更新日期:2019-08-01 00:00:00

  • Different patterns of spinal cyclooxygenase-1 and cyclooxygenase-2 mRNA expression in inflammatory and postoperative pain.

    abstract::Levels of cyclooxygenase-2 (COX-2) mRNA, but not those of COX-1, were reported to be raised significantly after peripheral inflammation in the rat spinal cord. The aim of the present study was to ascertain whether this pattern of COX-2 and COX-1 expression applies also to other pain conditions induced by surgical proc...

    journal_title:Basic & clinical pharmacology & toxicology

    pub_type: 杂志文章

    doi:10.1111/j.1742-7843.2006.pto_457.x

    authors: Prochazkova M,Dolezal T,Sliva J,Krsiak M

    更新日期:2006-08-01 00:00:00

  • Flaws in design, execution and interpretation limit CLARITY-BPA's value for risk assessments of bisphenol A.

    abstract::The Consortium Linking Academic and Regulatory Insights on BPA Toxicity (CLARITY-BPA) involved the Food and Drug Administration, the National Toxicology Program and 14 academic investigators funded by the National Institute of Environmental Health Sciences. Two key questions to be answered by CLARITY-BPA were as follo...

    journal_title:Basic & clinical pharmacology & toxicology

    pub_type: 杂志文章,评审

    doi:10.1111/bcpt.13195

    authors: Vom Saal FS

    更新日期:2019-08-01 00:00:00

  • Influence of endotoxin-induced sepsis on the requirements of propofol-fentanyl infusion rate in pigs.

    abstract::Endotoxin-induced sepsis in pigs is a recognized experimental model for the study of human septic shock. Generally, pigs are brought into general anaesthesia before sepsis is induced. It is our experience that drug dosages of propofol and fentanyl need to be reduced during endotoxin-induced sepsis, in order to prevent...

    journal_title:Basic & clinical pharmacology & toxicology

    pub_type: 杂志文章

    doi:10.1111/j.1742-7843.2007.00099.x

    authors: Bollen PJ,Nielsen BJ,Toft P

    更新日期:2007-09-01 00:00:00

  • Toxic Epidermal Necrolysis After Exposure to Dithiocarbamate Fungicide Mancozeb.

    abstract::Toxic epidermal necrolysis (TEN) is a life-threatening mucocutaneous disease with high mortality. Dithiocarbamates (DTC) are organosulphur compounds widely used in agriculture, industry and households. We report a case of TEN after exposure to mancozeb in fungicide. A 48-year-old 75 kg b.w. man was admitted with fever...

    journal_title:Basic & clinical pharmacology & toxicology

    pub_type: 杂志文章

    doi:10.1111/bcpt.12430

    authors: Zakharov S,Csomor J,Urbanek P,Pelclova D

    更新日期:2016-01-01 00:00:00

  • Herbal or natural medicines as modulators of peroxisome proliferator-activated receptors and related nuclear receptors for therapy of metabolic syndrome.

    abstract::The use of herbal or natural medicines for the treatment of various disorders has a long and extensive history. Many of these herbal medicines are finding their way onto the world market as alternatives to prescribed drugs currently available to treat various disorders/ailments. In particular, hyperlipidaemia is a maj...

    journal_title:Basic & clinical pharmacology & toxicology

    pub_type: 杂志文章,评审

    doi:10.1111/j.1742-7843.2005.pto960102.x

    authors: Huang TH,Kota BP,Razmovski V,Roufogalis BD

    更新日期:2005-01-01 00:00:00

  • Genetic, clinical and behavioural determinants of vitamin K-antagonist dose--explored through multivariable modelling and visualization.

    abstract::Vitamin K antagonists (VKA) are highly effective anticoagulants but their use is hampered by multiple interactions with food and medicine and a narrow therapeutic range. The large variation in dose requirements has led to the development of several dosing algorithms based on pharmacogenetic and clinical variables. In ...

    journal_title:Basic & clinical pharmacology & toxicology

    pub_type: 杂志文章

    doi:10.1111/j.1742-7843.2011.00789.x

    authors: Skov J,Bladbjerg EM,Rasmussen MA,Sidelmann JJ,Leppin A,Jespersen J

    更新日期:2012-02-01 00:00:00

  • Addiction-related effects of DOV 216,303 and cocaine: A comparative study in the mouse.

    abstract::DOV 216,303, an inhibitor of serotonin, noradrenaline and dopamine reuptake, belongs to a new line of drugs called 'triple reuptake inhibitors' that have been proposed for treatment of depression. The addictive drug cocaine has similar mechanism of action and exerts rewarding effects by blocking reuptake of dopamine, ...

    journal_title:Basic & clinical pharmacology & toxicology

    pub_type: 杂志文章

    doi:10.1111/bcpt.12182

    authors: Sørensen G,Husum H,Brennum LT,Bundgaard C,Montezinho LC,Mørk A,Wörtwein G,Woldbye DP

    更新日期:2014-06-01 00:00:00

  • Cardioprotective and cardiotoxic effects of quercetin and two of its in vivo metabolites on differentiated h9c2 cardiomyocytes.

    abstract::Whilst mitotic rat embryonic cardiomyoblast-derived H9c2 cells have been widely used as a model system to study the protective mechanisms associated with flavonoids, they are not fully differentiated cardiac cells. Hence, the aim of this study was to investigate the cardioprotective and cardiotoxic actions of querceti...

    journal_title:Basic & clinical pharmacology & toxicology

    pub_type: 杂志文章

    doi:10.1111/bcpt.12319

    authors: Daubney J,Bonner PL,Hargreaves AJ,Dickenson JM

    更新日期:2015-02-01 00:00:00

  • A Novel Model of P-Glycoprotein Inhibitor Screening Using Human Small Intestinal Organoids.

    abstract::P-glycoprotein (P-gp), an important efflux transporter in intestine, regulates the bioavailability of orally taken drugs. To develop an in vitro model that preferably mimics the physiological microenvironment of human intestine, we employed the three-dimensionally (3D) cultured organoids from human normal small intest...

    journal_title:Basic & clinical pharmacology & toxicology

    pub_type: 杂志文章

    doi:10.1111/bcpt.12680

    authors: Zhao J,Zeng Z,Sun J,Zhang Y,Li D,Zhang X,Liu M,Wang X

    更新日期:2017-03-01 00:00:00

  • Fisetin, a dietary flavonoid, induces cell cycle arrest and apoptosis through activation of p53 and inhibition of NF-kappa B pathways in bladder cancer cells.

    abstract::There is an obvious urgent need to find effective and safe therapies to prevent both recurrence and progression of bladder cancer. In the present study, we report that fisetin-induced apoptosis in human bladder cancer is mediated via modulation of two related pathways: up-regulation of p53 and down-regulation of NF-ka...

    journal_title:Basic & clinical pharmacology & toxicology

    pub_type: 杂志文章

    doi:10.1111/j.1742-7843.2010.00613.x

    authors: Li J,Cheng Y,Qu W,Sun Y,Wang Z,Wang H,Tian B

    更新日期:2011-02-01 00:00:00

  • Short-course vs long-course antibiotic treatment for community-acquired pneumonia: A literature review.

    abstract:BACKGROUND:It is well known that antibiotic use is the main driver for the increasing problems with resistant bacteria. Consequently, some countries have recommended shortening the duration of antibiotic treatment of community-acquired pneumonia (CAP). The aim of this study was to investigate whether the effectiveness ...

    journal_title:Basic & clinical pharmacology & toxicology

    pub_type: 杂志文章,评审

    doi:10.1111/bcpt.13205

    authors: Møller Gundersen K,Nygaard Jensen J,Bjerrum L,Hansen MP

    更新日期:2019-05-01 00:00:00

  • Paracelsus Revisited: The Dose Concept in a Complex World.

    abstract::At the time that Paracelsus coined his famous dictum, 'What is there that is not poison? All things are poison and nothing is without poison. Solely the dose determines that a thing is not a poison', embryonic toxicology was a fairly focused discipline that mainly dealt with occupational poisonings and side effects of...

    journal_title:Basic & clinical pharmacology & toxicology

    pub_type: 历史文章,杂志文章,评审

    doi:10.1111/bcpt.12622

    authors: Grandjean P

    更新日期:2016-08-01 00:00:00

  • Effects of antihypertensive and triglyceride-lowering agents on hepatic copper concentrations in rats with fatty liver disease.

    abstract::Copper deficiency had been suggested to link between fructose-enriched diet (FED) and the development of non-alcoholic fatty liver disease (NAFLD). In this study, we characterized changes in hepatic copper concentrations and hepatic oxidative milieu, in rats with the metabolic syndrome and NAFLD as a result of FED wit...

    journal_title:Basic & clinical pharmacology & toxicology

    pub_type: 杂志文章

    doi:10.1111/bcpt.12283

    authors: Ackerman Z,Skarzinski G,Grozovski M,Oron-Herman M,Sela BA

    更新日期:2014-12-01 00:00:00

  • Effect of caffeine-containing versus decaffeinated coffee on serum clozapine concentrations in hospitalised patients.

    abstract::Clozapine and caffeine are metabolised mainly by the cytochrome P4501A2 (CYP1A2) enzyme. Studies suggest that caffeine in coffee inhibits clozapine metabolism and increases serum clozapine concentrations. Our objective was to study whether coffee in the amounts usually consumed has an effect on steady-state serum cloz...

    journal_title:Basic & clinical pharmacology & toxicology

    pub_type: 临床试验,杂志文章,随机对照试验

    doi:

    authors: Raaska K,Raitasuo V,Laitila J,Neuvonen PJ

    更新日期:2004-01-01 00:00:00

  • Effects of the CYP2C9*1/*13 genotype on the pharmacokinetics of lornoxicam.

    abstract::Lornoxicam is extensively metabolized by CYP2C9, and a CYP2C9*13 is one of the principal variant alleles in East Asian populations. The aim of this study was to evaluate the effects of CYP2C9*1/*13 on the pharmacokinetic parameters of lornoxicam in healthy individuals. A single oral dose of 8 mg lornoxicam was given t...

    journal_title:Basic & clinical pharmacology & toxicology

    pub_type: 临床试验,杂志文章

    doi:10.1111/j.1742-7843.2011.00751.x

    authors: Choi CI,Kim MJ,Jang CG,Park YS,Bae JW,Lee SY

    更新日期:2011-12-01 00:00:00

  • Anticonvulsant and behavioural effects of the denatured venom of the social wasp Polybia occidentalis (Polistinae, Vespidae).

    abstract::Several investigations demonstrate that neurotoxins isolated from venoms of spiders and wasps may exert specific and selective activity on structures of the mammalian CNS. In the present work we examine the neurological effects of the low molecular weight compounds of the denatured venom of the neotropical social wasp...

    journal_title:Basic & clinical pharmacology & toxicology

    pub_type: 杂志文章

    doi:10.1111/j.1742-7843.2005.pto_137.x

    authors: Mortari MR,Cunha AO,de Oliveira L,Vieira EB,Gelfuso EA,Coutinho-Netto J,Ferreira dos Santos W

    更新日期:2005-11-01 00:00:00

  • Involvement of regulations of nucleophosmin and nucleoporins in gambogic acid-induced apoptosis in Jurkat cells.

    abstract::Gambogic acid, the main active compound of gamboge resin of Garcinia hanburryi, has recently exhibited marked antitumour potency on solid tumours of various derivations. We demonstrate here that gambogic acid also present powerful antileukaemic potency through both growth arrest and apoptosis induction in Jurkat cells...

    journal_title:Basic & clinical pharmacology & toxicology

    pub_type: 杂志文章

    doi:10.1111/j.1742-7843.2008.00292.x

    authors: Shu W,Chen Y,Li R,Wu Q,Cui G,Ke W,Chen Z

    更新日期:2008-12-01 00:00:00

  • Prenatal undernutrition changes renovascular responses of nimesulide in rat kidneys.

    abstract::Several studies in the Northeastern region of Brazil have demonstrated an association between hypertension in adult populations and prenatal and postnatal undernutrition. The central hypothesis we proposed was that hypertension could be favoured by programmed alterations in branches of the renal arachidonic pathway an...

    journal_title:Basic & clinical pharmacology & toxicology

    pub_type: 杂志文章

    doi:10.1111/j.1742-7843.2010.00625.x

    authors: Silva LA,Veira-Filho LD,Barreto IS,Cabral EV,Vieyra A,Paixão AD

    更新日期:2011-02-01 00:00:00

  • Predicting the outcome of phase III trials using phase II data: a case study of clinical trial simulation in late stage drug development.

    abstract::Maximizing the likelihood of success in Phase III is the ultimate goal of the use of modelling and simulation in the drug development process. The success in Phase III depends primarily on two questions: 1) Is the drug regimen actually efficacious and safe in the targeted patient population?, and 2) Will the planned P...

    journal_title:Basic & clinical pharmacology & toxicology

    pub_type: 杂志文章

    doi:10.1111/j.1742-7843.2005.pto960314.x

    authors: De Ridder F

    更新日期:2005-03-01 00:00:00

  • The effect of aggressive rosuvastatin treatment on steroid hormone production in men with coronary artery disease.

    abstract::Most steroid hormones are produced from cholesterol contained in low-density lipoproteins, which is uptaken by the gonads and adrenal cortex, and used as a substrate for steroidogenesis. Theoretically, in states associated with very low-density lipoprotein (LDL) cholesterol levels, cholesterol conversion to steroid ho...

    journal_title:Basic & clinical pharmacology & toxicology

    pub_type: 杂志文章

    doi:10.1111/bcpt.12169

    authors: Krysiak R,Okopien B

    更新日期:2014-04-01 00:00:00

  • Acidification alters antiarrhythmic drug blockade of the ether-a-go-go-related Gene (HERG) Channels.

    abstract::Acidosis is one of the important deleterious factors during myocardial ischaemia and reperfusion. The ether-a-go-go-related gene, HERG, is a primary target for blockade by many drugs including dofetilide, quinidine and azimilide. While most drugs lose their efficacy against arrhythmias associated with myocardial ischa...

    journal_title:Basic & clinical pharmacology & toxicology

    pub_type: 杂志文章

    doi:10.1111/j.1742-7843.2004.pto940503.x

    authors: Dong DL,Li Z,Wang HZ,Du ZM,Song WH,Yang BF

    更新日期:2004-05-01 00:00:00

  • Contribution of vasoactive eicosanoids and nitric oxide production to the effect of selective cyclooxygenase-2 inhibitor, NS-398, on endotoxin-induced hypotension in rats.

    abstract::Our previous studies with the use of non-selective cyclooxygenase (COX) inhibitor, indomethacin, demonstrated that prostanoids produced during endotoxaemia increase inducible nitric oxide synthase (iNOS) protein expression and nitric oxide synthesis, and decrease cyctochrome P450 (CYP) 4A1 protein expression and CYP 4...

    journal_title:Basic & clinical pharmacology & toxicology

    pub_type: 杂志文章

    doi:10.1111/j.1742-7843.2010.00589.x

    authors: Tunctan B,Korkmaz B,Cuez T,Kemal Buharalioglu C,Sahan-Firat S,Falck J,Malik KU

    更新日期:2010-11-01 00:00:00

  • Pre-clinical pharmacological profile of QF-036, a potent HIV-1 maturation inhibitor.

    abstract::QF-036 is an HIV-1 maturation inhibitor in pre-clinical development, and its antiviral activity against a laboratory HIV-1 strain and two drug-resistant strains was determined in the C8166 line. QF-036 was also subjected to absorption, distribution and metabolism (ADM) assessment in vitro, and pharmacokinetic profiles...

    journal_title:Basic & clinical pharmacology & toxicology

    pub_type: 杂志文章

    doi:10.1111/bcpt.13504

    authors: Zhao L,He HH,Ou-Yang T,Liu DF,Jiang CH,Yang HP,Wang P,Xie N,Yan SS

    更新日期:2021-02-01 00:00:00

  • Altered frequency distribution in the electroencephalogram is correlated to the analgesic effect of remifentanil.

    abstract::Opioids alter resting state brain oscillations by multiple and complex factors, which are still to be elucidated. To increase our knowledge, multi-channel electroencephalography (EEG) was subjected to multivariate pattern analysis (MVPA), to identify the most descriptive frequency bands and scalp locations altered by ...

    journal_title:Basic & clinical pharmacology & toxicology

    pub_type: 杂志文章,随机对照试验

    doi:10.1111/bcpt.12330

    authors: Graversen C,Malver LP,Kurita GP,Staahl C,Christrup LL,Sjøgren P,Drewes AM

    更新日期:2015-05-01 00:00:00

  • Which in vitro screens guide the prediction of oral absorption and volume of distribution?

    abstract::The development of medium to high-throughput in vitro screening of ADME (Absorption, Distribution, Metabolism, Excretion) properties has been the reply to higher demands on drug metabolism scientists to cope with progress in chemistry and biology. Two areas will be discussed here, namely screens for oral absorption an...

    journal_title:Basic & clinical pharmacology & toxicology

    pub_type: 杂志文章,评审

    doi:10.1111/j.1742-7843.2005.pto960304.x

    authors: van de Waterbeemd H

    更新日期:2005-03-01 00:00:00

  • In vivo pharmacological disease models for psoriasis and atopic dermatitis in drug discovery.

    abstract::In order to perform relevant in vivo pharmacological investigations in drug discovery within dermatology it is fundamental to master or have access to relevant skin disease models that makes it possible to identify and validate targets and to screen and discover drugs in vivo. There is a strong need for highly predict...

    journal_title:Basic & clinical pharmacology & toxicology

    pub_type: 杂志文章,评审

    doi:10.1111/j.1742-7843.2006.pto_298.x

    authors: Petersen TK

    更新日期:2006-08-01 00:00:00

  • The effects of inhibition of haem biosynthesis by griseofulvin on intestinal iron absorption.

    abstract::The relationship between haem biosynthesis and intestinal iron absorption in mice was investigated by ascertaining the effect of the haem synthesis inhibitor, griseofulvin, on duodenal iron absorption using both in vivo and in vitro measurements. Urinary 5-aminolaevulinic acid levels were increased within 24 hr of fee...

    journal_title:Basic & clinical pharmacology & toxicology

    pub_type: 杂志文章

    doi:10.1111/j.1742-7843.2004.pto940402.x

    authors: Laftah AH,Raja KB,Beaumont N,Simpson RJ,Deacon A,Solanky N,Srai SK,Peters TJ

    更新日期:2004-04-01 00:00:00

  • Safety of administration of human butyrylcholinesterase and its conjugates with soman or VX in rats.

    abstract::We evaluated the effects of conjugated enzyme-nerve agent product resulting from the inhibition of bioscavenger human serum butyrylcholinesterase (Hu BChE) by nerve agents soman or VX. Rats were trained on a multiple Fixed-Ratio 32, Extinction 30 sec. (FR32, Ext30) schedule of food reinforcement and then injected (i.m...

    journal_title:Basic & clinical pharmacology & toxicology

    pub_type: 杂志文章

    doi:10.1111/j.1742-7843.2009.00508.x

    authors: Genovese RF,Sun W,Johnson CC,Ditargiani RC,Doctor BP,Saxena A

    更新日期:2010-05-01 00:00:00