Literature DB >> 2242022

Spermine toxicity and glutathione depletion in BHK-21/C13 cells.

V G Brunton1, M H Grant, H M Wallace.   

Abstract

Spermine, a polycationic amine, produced a dose-dependent inhibition of BHK-21/C13 cell growth. This response was not due to the extracellular metabolism of spermine by an amine oxidase found in bovine serum, as the toxicity was observed when the cells were grown in medium supplemented with horse serum. Three indices were used to monitor cell growth, cell number, protein content and [3H]thymidine incorporation into DNA. Spermine (2mM) caused significant reductions in all three measurements after a 6-8 hr exposure. The amine was rapidly taken up into the cells reaching levels 15-16-fold greater than in control cells within 2 hr. There was a rapid loss of intracellular reduced glutathione following exposure to toxic concentrations of spermine, which occurred before any effect on cell growth. Three methods for the determination of intracellular glutathione content were compared in this system. The effect on both cell growth and glutathione was reversible following removal of spermine from the extracellular medium. The possible mechanisms involved in this toxic response are discussed with particular reference to the depletion in intracellular reduced glutathione.

Entities:  

Mesh:

Substances:

Year:  1990        PMID: 2242022     DOI: 10.1016/0006-2952(90)90371-q

Source DB:  PubMed          Journal:  Biochem Pharmacol        ISSN: 0006-2952            Impact factor:   5.858


  11 in total

Review 1.  A free-radical hypothesis for the instability and evolution of genotype and phenotype in vitro.

Authors:  R E Parchment; K Natarajan
Journal:  Cytotechnology       Date:  1992       Impact factor: 2.058

2.  Cardiac responses to β-adrenoceptor stimulation is partly dependent on mitochondrial calcium uniporter activity.

Authors:  E Fernández-Sada; C Silva-Platas; C A Villegas; S L Rivero; B C Willis; N García; J R Garza; Y Oropeza-Almazán; C A Valverde; G Mazzocchi; C Zazueta; G Torre-Amione; G García-Rivas
Journal:  Br J Pharmacol       Date:  2014-07-01       Impact factor: 8.739

Review 3.  Sequestered end products and enzyme regulation: the case of ornithine decarboxylase.

Authors:  R H Davis; D R Morris; P Coffino
Journal:  Microbiol Rev       Date:  1992-06

4.  Investigation into cell growth on collagen/chondroitin-6-sulphate gels: the effect of crosslinking agents and diamines.

Authors:  C S Osborne; W H Reid; M H Grant
Journal:  J Mater Sci Mater Med       Date:  1997-04       Impact factor: 3.896

5.  The influence of crosslinking agents and diamines on the pore size, morphology and the biological stability of collagen sponges and their effect on cell penetration through the sponge matrix.

Authors:  M McKegney; I Taggart; M H Grant
Journal:  J Mater Sci Mater Med       Date:  2001-09       Impact factor: 3.896

Review 6.  A perspective of polyamine metabolism.

Authors:  Heather M Wallace; Alison V Fraser; Alun Hughes
Journal:  Biochem J       Date:  2003-11-15       Impact factor: 3.857

7.  Mechanisms of spermine toxicity in baby-hamster kidney (BHK) cells. The role of amine oxidases and oxidative stress.

Authors:  V G Brunton; M H Grant; H M Wallace
Journal:  Biochem J       Date:  1991-11-15       Impact factor: 3.857

8.  Polyamines in biological samples: rapid and robust quantification by solid-phase extraction online-coupled to liquid chromatography-tandem mass spectrometry.

Authors:  Christoph Magnes; Alexander Fauland; Edgar Gander; Sophie Narath; Maria Ratzer; Tobias Eisenberg; Frank Madeo; Thomas Pieber; Frank Sinner
Journal:  J Chromatogr A       Date:  2014-01-14       Impact factor: 4.759

9.  Growth-inhibitory effects of the chemopreventive agent indole-3-carbinol are increased in combination with the polyamine putrescine in the SW480 colon tumour cell line.

Authors:  E Ann Hudson; Lynne M Howells; Barbara Gallacher-Horley; Louise H Fox; Andreas Gescher; Margaret M Manson
Journal:  BMC Cancer       Date:  2003-01-14       Impact factor: 4.430

10.  Cytotoxic Mechanism of Excess Polyamines Functions through Translational Repression of Specific Proteins Encoded by Polyamine Modulon.

Authors:  Akihiko Sakamoto; Junpei Sahara; Gota Kawai; Kaneyoshi Yamamoto; Akira Ishihama; Takeshi Uemura; Kazuei Igarashi; Keiko Kashiwagi; Yusuke Terui
Journal:  Int J Mol Sci       Date:  2020-03-31       Impact factor: 5.923

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.