PubMed HealthSearch

PubMed · 6836571

Time course of the carbon tetrachloride-induced decrease in mitochondrial aldehyde dehydrogenase activity.

Abstract

Hepatic microsomal enzymes like cytochrome P-450 and glucose 6-phosphatase are inhibited after exposure to CCl4 in vivo. Since comparatively less is known about the effects of CCl4 on nonmicrosomal enzymes, we investigated the rapidity by which CCl4 inhibits the low Km mitochondrial aldehyde dehydrogenase (ALDH) isozyme, an enzyme known to be inhibited 24 hr after CCl4 treatment. The activity of this ALDH isozyme was significantly lowered 6 and 12 hr after a single 1 ml/kg intragastric dose of CCl4. The mitochondrial low Km ALDH specific activities exhibited a similar pattern of destruction/inhibition to the documented target enzyme microsomal cytochrome P-450 in that lowest values were observed 6 hr after CCl4. These values were 44 and 37% of control for cytochrome P-450 content and the low Km ALDH activity, respectively. Alcohol dehydrogenase activity, expressed as activity per gram liver, was depressed 12 hr after CCl4 dosing. Finally, the activity of the low Km cytosolic ALDH, the isozyme that metabolizes malondialdehyde at low concentrations, was not affected by CCl4 treatment. The CCl4-induced decline in the activity of the matrix ALDH isozyme occurs earlier than previously reported mitochondrial damage. The study of sensitive enzymes like the low Km ALDH may provide valuable information by which it may be possible to determine the relationship of the truly rapid biochemical effects of CCl4 such as microsomal lipid peroxidation with later effects on nonmicrosomal components.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

J J Hjelle, J H Grubbs, D G Beer, D R Petersen. 1983. Time course of the carbon tetrachloride-induced decrease in mitochondrial aldehyde dehydrogenase activity.. https://doi.org/10.1016/0041-008x(83)90220-x

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

Inhibition of gene expression by triple helix formation in hepatoma cells.

The aim of this study was to selectively inhibit human mitochondrial aldehyde dehydrogenase (ALDH2) gene expression by triple helix assembly. Eight 21-mer oligodeoxyribonucleotides were designed to bind to two purine-rich sequences in the 5'-flanking region of the human ALDH2 gene. Gel mobility shift assays showed that triplex formation is sequence-specific for the target duplex and the third strand oligonucleotide. In the presence of Mg2+, but absence of K+, triplex-forming oligonucleotides bind to their target sites with apparent dissociation constants (Kd) in the 10(-7) to 10(-9) M range. Potassium cation virtually suppressed the triplex formation of G-C-rich duplex DNA with natural oligonucleotides, but did not prevent triplex formation with phosphorothioate-modified oligonucleotides. Phosphorothioate-modified oligonucleotides were delivered into human hepatoma Hep G2 cells by cationic liposomes. The reduction in ALDH2 mRNA levels in the cells was determined by the competitive reverse transcription-polymerase chain reaction. One of the phosphorothioate-modified oligonucleotides designed to forma an antiparallel triplex with a target in the 5'-flanking region of human ALDH2 gene (-105 to -125 from the translation initiation codon ATG) reduced by 80-90% the ALDH2 mRNA levels without affecting albumin mRNA levels. Data suggest that triple-helix formation may provide a means to selectively inhibit hepatic ALDH2 gene expression for therapeutic use.

Aldehyde Dehydrogenase

Comparative assessment of metabolic enzyme levels in macrophage populations of the F344 rat.

The immune system is a direct target for toxic insult by a number of drugs and other chemicals, many of which require activation to toxic metabolites by drug-metabolizing enzymes. We compared the induction of drug-metabolizing enzymes, including cytochrome P450 1A1 (CYP1A1) and aldehyde dehydrogenase (ALDH), which are differentially expressed in various macrophage populations following treatment of F344 rats with the inducer 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD). Kupffer cells, alveolar macrophages and splenic macrophages from TCDD-treated animals expressed elevated levels of inducible CYP1A1 as compared to other macrophage subpopulations or cells from control rats. TCDD treatment also resulted in increased ethoxyresorufin-O-deethylase (EROD) activity and total cytochrome P450 content in tissue-derived macrophages. Immunoreactive protein and mRNA transcripts for CYP1A1 were not detectable in resident peritoneal macrophages or peripheral blood monocytes. Examination of aromatic hydrocarbon receptor (AhR) levels in macrophage populations suggests that the ability of TCDD to induce metabolic enzymes in specific cell types correlates well with AhR expression. In vivo activation of macrophages, using either Bacillus of Calmette and Guérin, Mycobacterium tuberculosis (BCG) or polyinosinic:polycytidylic acid (Poly I:C), caused no significant alteration in the levels of induction of CYP1A1. ALDH-3 induction was similar in all macrophage populations examined. These studies indicate that macrophages, particularly those from portals of entry, may be induced to produce increased levels of specific enzymes, and the induction is dependent upon their maturational stage rather than their activation state. The metabolism of xenobiotics to toxic intermediates by immune cells and its role in immunosuppression are discussed.

Aldehyde Dehydrogenase

Identification of protein-receptor components required for the import of prealdehyde dehydrogenase into rat liver mitochondria.

Mitochondrial aldehyde dehydrogenase is synthesized as a high-molecular-weight precursor in cytosol and transported into mitochondrial matrix space where it is processed to the mature enzyme. To identify components of the transport machinery on liver mitochondria, anti-idiotypic antibodies against the rabbit anti-prealdehyde dehydrogenase signal peptide antibodies were produced in chicken eggs and rabbit. Both anti-idiotypic antibodies inhibited the import of prealdehyde dehydrogenase (pALDH) into isolated rat liver mitochondria. The rabbit anti-idiotypic antibody could recognize by Western blotting five mitochondrial membrane proteins with apparent molecular weights of 66, 60, 42, 34, and 29 kDa. The anti-idiotypic antibodies were cross-linked to mitochondrial membrane proteins using sulfosuccinimidyl 2-(p-azidosalicylamido)ethyl-1,3'-dithiopropionate which is an iodinatable, heterofunctional, and photoreactive cross-linker. Mitochondrial proteins with apparent molecular weights of 66, 60, and 42 kDa were identified using the chicken antibody. The 66- and 34-kDa proteins were cross-linked to the rabbit antibody as the major components and the 42-kDa protein as a minor one. Antibodies against the 60- and 42-kDa proteins, as well as Fab fragments, inhibited the import of pALDH, suggesting that these proteins are receptor/translocator components for pALDH import.

Aldehyde Dehydrogenase