Inhibition of mitochondrial respiration by cationic rhodamines as a possible teratogenicity mechanism.

Abstract:

:Exposure of mice to cationic rhodamines, Rh 123 and Rh 6G, has been found to be associated with developmental toxicity, while neutral rhodamines (e.g., Rh B) had no such effect. When mouse embryos from dams given ip injections of Rh 123, Rh 6G (15 mg/kg), or Rh B (30 mg/kg) on gestation Day (GD) 10 were examined, Rh 123, Rh 6G were present in embryonic tissue in fluorescent bodies within the average dimensions of mitochondria. Rh B was evenly distributed in the cytoplasm. With in vitro exposure of isolated mitochondria to rhodamines on GD 12, 3-4 times more Rh 123 was associated with mitochondria under energized conditions than under nonenergized conditions; the amount of Rh 6G associated with mitochondria was much less under either condition. Treatment of pregnant mice (ip) with Rh 123 (15 mg/kg/day) or Rh 6G (0.5 mg/kg/day) on GD 7-10 resulted in inhibition of state 3 respiration of embryonic mitochondria isolated on GD 12. When isolated embryonic mitochondria were exposed to the cationic rhodamines, inhibition of state 3 respiration was dose dependent. With 5 micrograms of Rh 123/mg mitochondrial protein, state 3 respiration decreased by 31%, while Rh 6G (1 microgram/mg) decreased state 3 respiration by 27%. In vivo exposure of maternal liver mitochondria to cationic rhodamines did not result in inhibition of respiration 2 days later, whereas in vitro results were similar to those for embryonic mitochondria. In vivo or in vitro exposure to Rh B had no effects on mitochondrial respiration. These results indicate that interference with embryonic energy metabolism is a possible mechanism by which cationic rhodamines exert adverse effects on embryogenesis.

journal_name

Toxicol Appl Pharmacol

authors

Ranganathan S,Churchill PF,Hood RD

doi

10.1016/0041-008x(89)90113-0

subject

Has Abstract

pub_date

1989-06-01 00:00:00

pages

81-9

issue

1

eissn

0041-008X

issn

1096-0333

journal_volume

99

pub_type

杂志文章
  • The common inhaled anesthetic isoflurane increases aggregation of huntingtin and alters calcium homeostasis in a cell model of Huntington's disease.

    abstract::Isoflurane is known to increase β-amyloid aggregation and neuronal damage. We hypothesized that isoflurane will have similar effects on the polyglutamine huntingtin protein and will cause alterations in intracellular calcium homeostasis. We tested this hypothesis in striatal cells from the expanded glutamine huntingti...

    journal_title:Toxicology and applied pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.taap.2010.10.032

    authors: Wang Q,Liang G,Yang H,Wang S,Eckenhoff MF,Wei H

    更新日期:2011-02-01 00:00:00

  • Hypoxia perturbs aryl hydrocarbon receptor signaling and CYP1A1 expression induced by PCB 126 in human skin and liver-derived cell lines.

    abstract::The aryl hydrocarbon receptor (AhR) is an important mediator of toxic responses after exposure to xenobiotics including 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) and dioxin-like polychlorinated biphenyls (PCBs). Activation of AhR responsive genes requires AhR dimerization with the aryl hydrocarbon receptor nuclear tr...

    journal_title:Toxicology and applied pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.taap.2013.12.002

    authors: Vorrink SU,Severson PL,Kulak MV,Futscher BW,Domann FE

    更新日期:2014-02-01 00:00:00

  • Alteration of programmed cell death and gene expression by 5-bromodeoxyuridine during limb development in mice.

    abstract::Some chemicals are known to induce limb malformations in mice. The occurrence of limb abnormality induced by chemical reagents is due to changes in the programmed cell death (PCD). 5-Bromodeoxyuridine (BrdU) is known as a potent teratogen and has been reported to induce polydactyly and other limb malformations in rode...

    journal_title:Toxicology and applied pharmacology

    pub_type: 杂志文章

    doi:10.1006/taap.2000.8989

    authors: Nakamura N,Fujioka M,Mori C

    更新日期:2000-09-01 00:00:00

  • Increased neutrophil adherence to endothelial cells exposed to asbestos.

    abstract::Inhalation of asbestos may activate the pulmonary endothelium to promote an inflammatory cell phenotype that participates in the development of pulmonary fibrosis. However, little is known about the effects of asbestos on endothelial cell function. Therefore, endothelial cells were exposed to chrysotile and crocidolit...

    journal_title:Toxicology and applied pharmacology

    pub_type: 杂志文章

    doi:10.1006/taap.1996.0143

    authors: Treadwell MD,Mossman BT,Barchowsky A

    更新日期:1996-07-01 00:00:00

  • Role of mitogen activated protein kinases in skin tumorigenicity of patulin.

    abstract::WHO has highlighted the need to evaluate dermal toxicity of mycotoxins including Patulin (PAT), detected in several fruits. In this study the skin carcinogenic potential of topically applied PAT was investigated. Single topical application of PAT (400 nmol) showed enhanced cell proliferation (~2 fold), along with incr...

    journal_title:Toxicology and applied pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.taap.2011.09.012

    authors: Saxena N,Ansari KM,Kumar R,Chaudhari BP,Dwivedi PD,Das M

    更新日期:2011-12-01 00:00:00

  • Benzoquinone inhibits the voltage-dependent induction of the mitochondrial permeability transition caused by redox-cycling naphthoquinones.

    abstract::The mitochondrial permeability pore is subject to regulation by a thiol-dependent voltage sensor (Petronilli, V., Costantini, P., Scorrano, L., Colonna, R., Passamonti, S., and Bernardi, P., J. Biol. Chem. 269, 16638-16642, 1994); thiol oxidation increases the gating potential, which increases the probability of pore ...

    journal_title:Toxicology and applied pharmacology

    pub_type: 杂志文章

    doi:10.1006/taap.1996.8099

    authors: Palmeira CM,Wallace KB

    更新日期:1997-04-01 00:00:00

  • Protective effects of ursodeoxycholic acid against 2,3,7,8-tetrachlorodibenzo-p-dioxin-induced testicular damage in mice.

    abstract::The protective effect of ursodeoxycholic acid (UDCA), a biliary component found in bears, on 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD)-induced testicular damage in mice was investigated. Fifty C57BL/6J mice were equally divided into five groups. The mice in the control group received the vehicle and standard chow. Th...

    journal_title:Toxicology and applied pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.taap.2003.09.024

    authors: Kwon YI,Yeon JD,Oh SM,Chung KH

    更新日期:2004-02-01 00:00:00

  • Phenylbutyric acid protects against carbon tetrachloride-induced hepatic fibrogenesis in mice.

    abstract::A recent report showed that the unfolded protein response (UPR) signaling was activated in the pathogenesis of carbon tetrachloride (CCl(4))-induced hepatic fibrosis. Phenylbutyric acid (PBA) is a well-known chemical chaperone that inhibits endoplasmic reticulum (ER) stress and unfolded protein response (UPR) signalin...

    journal_title:Toxicology and applied pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.taap.2012.11.007

    authors: Wang JQ,Chen X,Zhang C,Tao L,Zhang ZH,Liu XQ,Xu YB,Wang H,Li J,Xu DX

    更新日期:2013-01-15 00:00:00

  • Dual effect of insulin resistance and cadmium on human granulosa cells - In vitro study.

    abstract::Combined exposure of cadmium (Cd) and insulin resistance (IR) might be responsible for subfertility. In the present study, we investigated the effects of Cd in vitro in IR human granulosa cells. Isolated human granulosa cells from control and polycystic ovary syndrome (PCOS) follicular fluid samples were confirmed for...

    journal_title:Toxicology and applied pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.taap.2016.10.019

    authors: Belani M,Shah P,Banker M,Gupta S

    更新日期:2016-12-15 00:00:00

  • Liposomal formulation of alpha-tocopheryl maleamide: in vitro and in vivo toxicological profile and anticancer effect against spontaneous breast carcinomas in mice.

    abstract::The vitamin E analogue alpha-tocopheryl succinate (alpha-TOS) is an efficient anti-cancer drug. Improved efficacy was achieved through the synthesis of alpha-tocopheryl maleamide (alpha-TAM), an esterase-resistant analogue of alpha-tocopheryl maleate. In vitro tests demonstrated significantly higher cytotoxicity of al...

    journal_title:Toxicology and applied pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.taap.2009.01.027

    authors: Turánek J,Wang XF,Knötigová P,Koudelka S,Dong LF,Vrublová E,Mahdavian E,Procházka L,Sangsura S,Vacek A,Salvatore BA,Neuzil J

    更新日期:2009-06-15 00:00:00

  • Herb-drug interaction prediction based on the high specific inhibition of andrographolide derivatives towards UDP-glucuronosyltransferase (UGT) 2B7.

    abstract::Herb-drug interaction strongly limits the clinical application of herbs and drugs, and the inhibition of herbal components towards important drug-metabolizing enzymes (DMEs) has been regarded as one of the most important reasons. The present study aims to investigate the inhibition potential of andrographolide derivat...

    journal_title:Toxicology and applied pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.taap.2014.02.021

    authors: Ma HY,Sun DX,Cao YF,Ai CZ,Qu YQ,Hu CM,Jiang C,Dong PP,Sun XY,Hong M,Tanaka N,Gonzalez FJ,Ma XC,Fang ZZ

    更新日期:2014-05-15 00:00:00

  • The use of proton nuclear magnetic resonance spectrometry (1H NMR) for monitoring the reaction of epoxides with butylamine and predictive capabilities of the relative alkylation index (RAI) for skin sensitization by epoxides.

    abstract::A group of alkyl epoxides was compared for their guinea pig sensitization capacity and reactivities towards a protein-surrogate substrate, n-butylamine. Instead of the previously reported use of a titration method for determination of alkylation rate, proton nuclear magnetic resonance spectrometry (1H NMR) was used. T...

    journal_title:Toxicology and applied pharmacology

    pub_type: 杂志文章

    doi:10.1016/0041-008x(91)90094-u

    authors: Betso JE,Carreon RE,Miner VM

    更新日期:1991-05-01 00:00:00

  • Mefenamic acid bi-directionally modulates the transient outward K+ current in rat cerebellar granule cells.

    abstract::The effect of non-steroidal anti-inflammatory drugs (NSAIDs) on ion channels has been widely studied in several cell models, but less is known about their modulatory mechanisms. In this report, the effect of mefenamic acid on voltage-activated transient outward K(+) current (I(A)) in cultured rat cerebellar granule ce...

    journal_title:Toxicology and applied pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.taap.2007.09.008

    authors: Zhang M,Shi WJ,Fei XW,Liu YR,Zeng XM,Mei YA

    更新日期:2008-02-01 00:00:00

  • Down-regulation of the detoxifying enzyme NAD(P)H:quinone oxidoreductase 1 by vanadium in Hepa 1c1c7 cells.

    abstract::Recent data suggest that vanadium (V5+) compounds exert protective effects against chemical-induced carcinogenesis, mainly through modifying various xenobiotic metabolizing enzymes. In fact, we have shown that V5+ down-regulates the expression of Cyp1a1 at the transcriptional level through an ATP-dependent mechanism. ...

    journal_title:Toxicology and applied pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.taap.2009.02.002

    authors: Anwar-Mohamed A,El-Kadi AO

    更新日期:2009-05-01 00:00:00

  • Inhibition of Na,K-ATPase by cadmium: different mechanisms in different species.

    abstract::The mechanism of action of Cd on Na,K-ATPase was investigated in two "classical" model systems, the shark rectal gland and rabbit kidney outer medulla. In lyophilized plasma membranes from dogfish rectal gland Cd inhibited Na,K-ATPase activity after 30 min of preincubation with an I50 of 1.3 x 10(-5) M. K-Dependent p-...

    journal_title:Toxicology and applied pharmacology

    pub_type: 杂志文章

    doi:10.1006/taap.1993.1124

    authors: Kinne-Saffran E,Hülseweh M,Pfaff C,Kinne RK

    更新日期:1993-07-01 00:00:00

  • Gypenoside XLIX, a naturally occurring gynosaponin, PPAR-alpha dependently inhibits LPS-induced tissue factor expression and activity in human THP-1 monocytic cells.

    abstract::Tissue factor (TF) is involved not only in the progression of atherosclerosis and other cardiovascular diseases, but is also associated with tumor growth, metastasis, and angiogenesis and hence may be an attractive target for directed cancer therapeutics. Gynostemma pentaphyllum (GP) is widely used in the treatment of...

    journal_title:Toxicology and applied pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.taap.2006.10.013

    authors: Huang TH,Tran VH,Roufogalis BD,Li Y

    更新日期:2007-01-01 00:00:00

  • Refinement and verification of the physiologically based dosimetry description for acrylonitrile in rats.

    abstract::The physiologically based dosimetry description for acrylonitrile (ACN) and its mutagenic epoxide metabolite 2-cyanoethylene oxide (CEO) in F-344 rats (M. L. Gargas, M. E. Anderson, S.K.O. Teo, R. Batra, T. R. Fennell, and G. L. Kedderis, 1995, Toxicol. Appl. Pharmacol. 134, 185-194) has been refined to include a phys...

    journal_title:Toxicology and applied pharmacology

    pub_type: 杂志文章

    doi:10.1006/taap.1996.0239

    authors: Kedderis GL,Teo SK,Batra R,Held SD,Gargas ML

    更新日期:1996-10-01 00:00:00

  • Selective inhibition of phospholipases by atiprimod, a macrophage targeting antiarthritic compound.

    abstract::Azaspiranes are cationic amphiphilic compounds that are active in a number of models of autoimmune disease and transplantation. Repeated administration of cationic amphiphiles induces phospholipid accumulation in a variety of species. The present study was conducted to explore the mechanism of phospholipid accumulatio...

    journal_title:Toxicology and applied pharmacology

    pub_type: 杂志文章

    doi:10.1006/taap.1999.8732

    authors: Handler JA,Badger A,Genell CA,Klinkner AM,Kassis S,Waites CR,Bugelski PJ

    更新日期:1999-08-15 00:00:00

  • Arsenic, mode of action at biologically plausible low doses: what are the implications for low dose cancer risk?

    abstract::Arsenic is an established human carcinogen. However, there has been much controversy about the shape of the arsenic response curve, particularly at low doses. This controversy has been exacerbated by the fact that the mechanism(s) of arsenic carcinogenesis are still unclear and because there are few satisfactory anima...

    journal_title:Toxicology and applied pharmacology

    pub_type: 杂志文章,评审

    doi:10.1016/j.taap.2005.01.048

    authors: Snow ET,Sykora P,Durham TR,Klein CB

    更新日期:2005-09-01 00:00:00

  • Autophagy blockade sensitizes the anticancer activity of CA-4 via JNK-Bcl-2 pathway.

    abstract::Combretastatin A-4 (CA-4) has already entered clinical trials of solid tumors over ten years. However, the limited anticancer activity and dose-dependent toxicity restrict its clinical application. Here, we offered convincing evidence that CA-4 induced autophagy in various cancer cells, which was demonstrated by acrid...

    journal_title:Toxicology and applied pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.taap.2013.11.018

    authors: Li Y,Luo P,Wang J,Dai J,Yang X,Wu H,Yang B,He Q

    更新日期:2014-01-15 00:00:00

  • Inhibition of proliferative activity of pulmonary fibroblasts by tetrandrine.

    abstract::Tetrandrine, an herbal drug, has been employed in China to treat pulmonary fibrosis. To date, the mechanisms governing the antifibrotic action of tetrandrine are unknown. The present study employs a fibroblast mitogenic assay to determine whether tetrandrine directly inhibits the ability of fibroblasts to respond to s...

    journal_title:Toxicology and applied pharmacology

    pub_type: 杂志文章

    doi:10.1006/taap.1993.1173

    authors: Reist RH,Dey RD,Durham JP,Rojanasakul Y,Castranova V

    更新日期:1993-09-01 00:00:00

  • The fate of inhaled octane and the nephrotoxicant, isooctane, in rats.

    abstract::To determine if inhaled nephrotoxic branched and nonnephrotoxic straight chain alkanes differ substantially in their biological fate, male F344 rats were exposed to 14C-labeled isooctane and octane vapors at approximately 1 and 350 ppm by the nose-only mode for 2 hr. Radioactivity in exhalant, urine, and feces was det...

    journal_title:Toxicology and applied pharmacology

    pub_type: 杂志文章

    doi:10.1016/0041-008x(89)90319-0

    authors: Dahl AR

    更新日期:1989-09-01 00:00:00

  • Dynamic and accurate assessment of acetaminophen-induced hepatotoxicity by integrated photoacoustic imaging and mechanistic biomarkers in vivo.

    abstract::The prediction and understanding of acetaminophen (APAP)-induced liver injury (APAP-ILI) and the response to therapeutic interventions is complex. This is due in part to sensitivity and specificity limitations of currently used assessment techniques. Here we sought to determine the utility of integrating translational...

    journal_title:Toxicology and applied pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.taap.2017.07.019

    authors: Brillant N,Elmasry M,Burton NC,Rodriguez JM,Sharkey JW,Fenwick S,Poptani H,Kitteringham NR,Goldring CE,Kipar A,Park BK,Antoine DJ

    更新日期:2017-10-01 00:00:00

  • Reversal of saxitoxin-induced cardiorespiratory failure by a burro-raised alpha-STX antibody and oxygen therapy.

    abstract::Reversal of saxitoxin (STX; 10 micrograms/kg, ip) induced cardiorespiratory effects by oxygen ventilation and burro-raised alpha-STX antitoxin (60 mg/kg, i.v.) was studied in urethane-anesthetized guinea pigs acutely instrumented for concurrent monitoring of medullary respiratory-related single units, diaphragm EMG, L...

    journal_title:Toxicology and applied pharmacology

    pub_type: 杂志文章

    doi:10.1006/taap.1994.1006

    authors: Benton BJ,Rivera VR,Hewetson JF,Chang FC

    更新日期:1994-01-01 00:00:00

  • Effect of metallothionein core promoter region polymorphism on cadmium, zinc and copper levels in autopsy kidney tissues from a Turkish population.

    abstract::Metallothioneins (MTs) are metal-binding, low molecular weight proteins and are involved in pathophysiological processes like metabolism of essential metals, metal ion homeostasis and detoxification of heavy metals. Metallothionein expression is induced by various heavy metals especially cadmium, mercury and zinc; MTs...

    journal_title:Toxicology and applied pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.taap.2010.03.007

    authors: Kayaalti Z,Mergen G,Söylemezoğlu T

    更新日期:2010-06-01 00:00:00

  • Gallic acid-capped gold nanoparticles inhibit EGF-induced MMP-9 expression through suppression of p300 stabilization and NFκB/c-Jun activation in breast cancer MDA-MB-231 cells.

    abstract::Triple-negative breast cancers (TNBCs) are highly invasive and have a higher rate of distant metastasis. Matrix metalloproteinase-9 (MMP-9) plays a crucial role in EGF/EGFR-mediated malignant progression and metastasis of TNBCs. Various studies have revealed that treatment with gallic acid down-regulates MMP-9 express...

    journal_title:Toxicology and applied pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.taap.2016.09.007

    authors: Chen YJ,Lee YC,Huang CH,Chang LS

    更新日期:2016-11-01 00:00:00

  • Measurement of elongate mineral particles: What we should measure and how do we do it?

    abstract::The length distributions of single fibrils of Coalinga, UICC-B and wet dispersed chrysotile were measured by transmission electron microscopy (TEM). It was found that the distributions significantly diverged above approximately 10 μm (μm) in length, corresponding to differences in published results of animal experimen...

    journal_title:Toxicology and applied pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.taap.2018.08.010

    authors: Chatfield EJ

    更新日期:2018-12-15 00:00:00

  • Metabolomic and proteomic biomarkers for III-V semiconductors: chemical-specific porphyrinurias and proteinurias.

    abstract::A pressing need exists to develop and validate molecular biomarkers to assess the early effects of chemical agents, both individually and in mixtures. This is particularly true for new and chemically intensive industries such as the semiconductor industry. Previous studies from this laboratory and others have demonstr...

    journal_title:Toxicology and applied pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.taap.2005.01.020

    authors: Fowler BA,Conner EA,Yamauchi H

    更新日期:2005-08-07 00:00:00

  • Effect of JP-8 jet fuel on molecular and histological parameters related to acute skin irritation.

    abstract::Organic chemicals such as jet fuels and solvents can cause skin irritation after dermal exposure. The molecular responses to these chemicals resulting in acute irritation are not understood well enough to establish safe exposure limits. Male F-344 rats were dermally exposed to JP-8 jet fuel for 1 h using Hill Top Cham...

    journal_title:Toxicology and applied pharmacology

    pub_type: 杂志文章

    doi:10.1006/taap.2001.9248

    authors: Kabbur MB,Rogers JV,Gunasekar PG,Garrett CM,Geiss KT,Brinkley WW,McDougal JN

    更新日期:2001-08-15 00:00:00

  • Coenzyme Q10 and alpha-tocopherol protect against amitriptyline toxicity.

    abstract::Since amitriptyline is a very frequently prescribed antidepressant drug, it is not surprising that amitriptyline toxicity is relatively common. Amitriptyline toxic systemic effects include cardiovascular, autonomous nervous, and central nervous systems. To understand the mechanisms of amitriptyline toxicity we studied...

    journal_title:Toxicology and applied pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.taap.2008.12.026

    authors: Cordero MD,Moreno-Fernández AM,Gomez-Skarmeta JL,de Miguel M,Garrido-Maraver J,Oropesa-Avila M,Rodríguez-Hernández A,Navas P,Sánchez-Alcázar JA

    更新日期:2009-03-15 00:00:00