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1.
Br J Dermatol ; 171(1): 55-62, 2014 Jul.
Article in English | MEDLINE | ID: mdl-24471979

ABSTRACT

BACKGROUND: Animal studies report photodynamic therapy (PDT) to improve healing of excisional wounds; the mechanism is uncertain and equivalent human studies are lacking. OBJECTIVES: To explore the impact of methyl aminolaevulinate (MAL)-PDT on clinical and microscopic parameters of human cutaneous excisional wound healing, examining potential modulation through production of transforming growth factor (TGF)-ß isoforms. METHODS: In 27 healthy older men (60-77 years), a 4-mm punch biopsy wound was created in skin of the upper inner arm and treated with MAL-PDT three times over 5 days. An identical control wound to the contralateral arm was untreated and both wounds left to heal by secondary intention. Wounds were re-excised during the inflammatory phase (7 days, n = 10), matrix remodelling (3 weeks, n = 8) and cosmetic outcome/dermal structure (9 months, n = 9). Production of TGF-ß1, TGF-ß3 and matrix metalloproteinases (MMPs) was assessed by immunohistochemistry alongside microscopic measurement of wound size/area and clinical assessment of wound appearance. RESULTS: MAL-PDT delayed re-epithelialization at 7 days, associated with increased inflammation. However, 3 weeks postwounding, treated wounds were smaller with higher production of MMP-1 (P = 0·01), MMP-9 (P = 0·04) and TGF-ß3 (P = 0·03). TGF-ß1 was lower than control at 7 days and higher at 3 weeks (both P = 0·03). At 9 months, MAL-PDT-treated wounds showed greater, more ordered deposition of collagen I, collagen III and elastin (all P < 0·05). CONCLUSIONS: MAL-PDT increases MMP-1, MMP-9 and TGF-ß3 production during matrix remodelling, ultimately producing scars with improved dermal matrix architecture.


Subject(s)
Aminolevulinic Acid/analogs & derivatives , Matrix Metalloproteinase 1/biosynthesis , Matrix Metalloproteinase 9/biosynthesis , Photosensitizing Agents/administration & dosage , Skin/injuries , Transforming Growth Factor beta3/biosynthesis , Administration, Cutaneous , Aged , Aminolevulinic Acid/administration & dosage , Arm , Healthy Volunteers , Humans , Male , Photochemotherapy/methods , Re-Epithelialization/drug effects , Wound Healing/drug effects
3.
Br J Anaesth ; 104(6): 768-73, 2010 Jun.
Article in English | MEDLINE | ID: mdl-20418532

ABSTRACT

BACKGROUND: Lidocaine and bupivacaine are commonly infiltrated into surgical cutaneous wounds to provide local anaesthesia after surgical procedures. However, very little is known about their effects on cutaneous wound healing. If an inhibitory effect is demonstrated, then the balance between the benefits of postoperative local anaesthesia and the negatives of impaired cutaneous wound healing may affect the decision to use local anaesthesia or not. Furthermore, if a difference in the rate of healing of lidocaine- and bupivacaine-treated cutaneous wounds is revealed, or if an inhibitory effect is found to be dose-dependent, then this may well influence the choice of agent and its concentration for clinical use. METHODS: Immediately before incisional wounding, we administered lidocaine and bupivacaine intradermally to adult female mice, some of which had been ovariectomized to act as a model of post-menopausal women (like post-menopausal women, ovariectomized mice heal wounds poorly, with increased proteolysis and inflammation). Day 3 wound tissue was analysed histologically and tested for expression of inflammatory and proteolytic factors. RESULTS: On day 3 post-wounding, wound areas and extent of re-epithelialization were comparable between the control and local anaesthetic-treated animals, in both intact and ovariectomized groups. Both tested drugs significantly increased wound activity of the degradative enzyme matrix metalloproteinase-2 relative to controls, while lidocaine also increased wound neutrophil numbers. CONCLUSIONS: Although lidocaine and bupivacaine influenced local inflammatory and proteolytic factors, they did not impair the rate of healing in either of two well-established models (mimicking normal human wound healing and impaired age-related healing).


Subject(s)
Anesthetics, Local/pharmacology , Bupivacaine/pharmacology , Lidocaine/pharmacology , Skin/drug effects , Wound Healing/drug effects , Aging/physiology , Anesthetics, Local/administration & dosage , Animals , Bupivacaine/administration & dosage , Collagen/metabolism , Dermatologic Surgical Procedures , Disease Models, Animal , Dose-Response Relationship, Drug , Female , Lidocaine/administration & dosage , Mice , Mice, Inbred C57BL , Postmenopause/physiology , Skin/metabolism , Wound Healing/physiology
4.
J Pathol ; 217(1): 73-82, 2009 Jan.
Article in English | MEDLINE | ID: mdl-18855875

ABSTRACT

The ongoing search for explanations as to why elderly males heal acute skin wounds more slowly than do their female counterparts (and are more strongly disposed to conditions of chronic ulceration) has identified endogenous oestrogens and androgens as being respectively enhancers and inhibitors of repair. We previously demonstrated that blocking the conversion of testosterone to 5alpha-dihydrotestosterone (DHT) limits its ability to impair healing, suggesting that DHT is a more potent inhibitor of repair than is testosterone. The present study aimed to delineate the central mechanisms by which androgens delay repair. Whilst the contractile properties of neither rat wounds in vivo nor fibroblast-impregnated collagenous discs in vitro appeared to be influenced by androgen manipulations, the global blockade of DHT biosynthesis markedly accelerated re-epithelialization of incisional and excisional wounds and reduced local expression of beta-catenin, a key inhibitor of repair. Moreover, DHT retarded the in vitro migration of epidermal keratinocytes following scratch wounding. By contrast, it failed to influence the migratory and proliferative properties of dermal fibroblasts, suggesting that its primary inhibitory effect is upon re-epithelialization. These novel findings may be of particular significance in the context of chronic ulceration, for which being male is a key risk factor.


Subject(s)
Androgens/pharmacology , Dihydrotestosterone/pharmacology , Wound Healing/drug effects , 5-alpha Reductase Inhibitors , Animals , Cell Movement/drug effects , Cells, Cultured , Dihydrotestosterone/metabolism , Enzyme Inhibitors/pharmacology , Epidermis/drug effects , Epithelium/drug effects , Epithelium/metabolism , Finasteride/analogs & derivatives , Finasteride/pharmacology , Keratinocytes/drug effects , Keratinocytes/physiology , Male , Rats , Rats, Sprague-Dawley , Skin/drug effects , Skin/injuries , Skin/metabolism , Wound Healing/physiology , beta Catenin/metabolism
5.
Proc Natl Acad Sci U S A ; 98(23): 13031-6, 2001 Nov 06.
Article in English | MEDLINE | ID: mdl-11698679

ABSTRACT

Barrier activity of skin and internal barrier-forming epithelial linings are conferred by a lipid-corneocyte structure (stratum corneum in skin). The integrity of the corneocytes depends on the outer cornified envelope and is essential for maintenance of barrier function. During epidermal development and differentiation, proteins are sequentially incorporated into the envelope via action of epidermal transglutaminases in a well documented process. However, recent knockouts of major cornified envelope constituents have failed to disrupt barrier function significantly, suggesting that additional unidentified components are involved. We report a new gene cluster in the epidermal differentiation complex at human 1q21 encoding a family of 18 proteins that are substrates for epidermal transglutaminases. These proteins incorporate into the cornified envelope late in development and late in the process of envelope maturation during epidermal differentiation. The genes cluster within the epidermal differentiation complex according to expression pattern, i.e., epidermally expressed proteins cluster together while proteins from internal barrier-forming epithelia also cluster. We propose that these proteins modulate barrier activity over the surface of the animal, in a manner analogous to that proposed for the well characterized cornified envelope precursors, the small proline-rich proteins. To emphasize the incorporation of these proteins late in envelope assembly, we call the human proteins late envelope proteins.


Subject(s)
Epidermis/metabolism , Proteins/genetics , Animals , Base Sequence , Cell Differentiation/genetics , Chromosomes, Human, Pair 1 , DNA Primers , Epidermal Cells , Humans , Immunohistochemistry , Mice , Mice, Inbred ICR , Mice, Knockout , Multigene Family , Proteins/metabolism
6.
J Mol Biol ; 304(4): 575-84, 2000 Dec 08.
Article in English | MEDLINE | ID: mdl-11099381

ABSTRACT

N-terminal or C-terminal arms that extend from folded protein domains can play a critical role in quaternary structure and other intermolecular associations and/or in controlling biological activity. We have tested the role of an extended N-terminal arm in the structure and function of a periplasmic enzyme glucose-fructose oxidoreductase (GFOR) from Zymomonas mobilis. We have determined the crystal structure of the NAD(+) complex of a truncated form of the enzyme, GFORDelta, in which the first 22 residues of the N-terminal arm of the mature protein have been deleted. The structure, refined at 2.7 A resolution (R(cryst)=24.1%, R(free)=28.4%), shows that the truncated form of the enzyme forms a dimer and implies that the N-terminal arm is essential for tetramer formation by wild-type GFOR. Truncation of the N-terminal arm also greatly increases the solvent exposure of the cofactor; since GFOR activity is dependent on retention of the cofactor during the catalytic cycle we conclude that the absence of GFOR activity in this mutant results from dissociation of the cofactor. The N-terminal arm thus determines the quaternary structure and the retention of the cofactor for GFOR activity and during translocation into the periplasm. The structure of GFORDelta also shows how an additional mutation, Ser64Asp, converts the strict NADP(+) specificity of wild-type GFOR to a dual NADP(+)/NAD(+) specificity.


Subject(s)
Oxidoreductases/chemistry , Oxidoreductases/metabolism , Sequence Deletion , Zymomonas/enzymology , Amino Acid Sequence , Binding Sites , Crystallization , Crystallography, X-Ray , Dimerization , Hydrogen Bonding , Models, Molecular , NAD/metabolism , NADP/metabolism , Oxidoreductases/genetics , Protein Structure, Quaternary , Protein Structure, Secondary , Sequence Deletion/genetics , Solvents , Substrate Specificity
7.
J Invest Dermatol ; 114(5): 967-75, 2000 May.
Article in English | MEDLINE | ID: mdl-10771479

ABSTRACT

Stratified, terminally differentiated epithelia, such as epidermis and oral epithelia, provide protective barriers against the environment. We recently developed wholemount assays that demonstrate epidermal barrier function during late gestation and showed that epidermal barrier forms at specific sites (epidermal initiation sites), and then spreads around the body as apparent moving fronts. We now ask if this is a fundamental and widespread mode of epithelial developmental change. If so, then the pattern should be apparent when assaying for developmental change other than barrier institution (e.g., gene induction) and similar types of patterned change should be apparent in other types of epithelia. In this study we demonstrate patterned barrier function in a range of additional stratified epithelia from the oral cavity and show that the gene induction pattern of a stratum corneum precursor small proline-rich region protein 1 (SPRR1) precedes barrier function and occurs in the barrier pattern, i.e., gene induction occurs first at initiation sites and propagates across epithelia as apparent moving fronts. These results demonstrate that late gestational developmental change in multiple terminally differentiating epithelia occurs via initiation sites and moving fronts. The pattern precedes barrier formation and results in a developmental gradient that influences gene induction.


Subject(s)
Gene Expression Regulation , Mouth Mucosa/metabolism , Proteins/genetics , Animals , Cell Differentiation , Cornified Envelope Proline-Rich Proteins , Female , Membrane Proteins , Mice , Mice, Inbred ICR , Mouth Mucosa/cytology , Mouth Mucosa/embryology , Permeability , Pregnancy , Transcriptional Activation
8.
J Agric Food Chem ; 47(11): 4557-67, 1999 Nov.
Article in English | MEDLINE | ID: mdl-10552850

ABSTRACT

Dilute solutions of beta-lactoglobulin (beta-Lg) A, B, and C were heated in phosphate buffer at temperatures between 40 and 94 degrees C for 10 min, cooled, and analyzed using near-UV and far-UV circular dichroism (CD). The decrease in near-UV CD intensity at 293 nm (Deltaepsilon(293)) could be analyzed in terms of a two-state model, and the stability was beta-Lg C > beta-Lg A > beta-Lg B on the basis of the midpoint temperatures for samples heated at pH 6.7 and 7.4. However, the slopes of the curves at the midpoint temperature for variant A were generally less than those for beta-Lg B and beta-Lg C, indicating that the substitution of Val (beta-Lg A) for Ala (beta-Lg B or beta-Lg C) at position 118 had altered the entropic contribution to unfolding of the protein. The changes in CD at 270 nm (Deltaepsilon(270)), an index of significant alteration to disulfide bond dihedral angles, occurred at higher temperatures than those for the Deltaepsilon(293) results. The far-UV CD showed some small changes as a consequence of heat treatment, and the shifts at 205 nm ([theta](205)) fitted a two-state model. Plotting the changes in both Deltaepsilon(293) and [theta](205) against the loss of nativelike and sodium dodecyl sulfate-monomeric protein (assessed by polyacrylamide gel electrophoresis) showed a strong 1:1 relationship between Deltaepsilon(293) or [theta](205) and the loss of nativelike beta-Lg. These results indicated that the initial irreversible stage in the heat-induced aggregation of beta-Lg (nativelike monomer to unfolded monomer) altered the chirality of the environment of Trp(19) and modified the secondary structure of beta-Lg slightly. The differences in the behavior of variants A-C were explicable on the basis of generalized electrostatic and hydrophobicity effects as well as specific amino acid effects.


Subject(s)
Hot Temperature , Lactoglobulins/chemistry , Animals , Cattle , Circular Dichroism , Protein Conformation , Spectrophotometry, Ultraviolet
9.
J Invest Dermatol ; 113(6): 1106-13, 1999 Dec.
Article in English | MEDLINE | ID: mdl-10594759

ABSTRACT

We recently demonstrated patterned stratum corneum maturation and skin barrier formation during fetal development in rodents and rabbit. The presence of skin patterning in these mammals led us to predict patterned barrier formation during human infant development. Here we extend our mammalian study and demonstrate patterned stratum corneum development and skin barrier formation in the pre-term human infant. Surprisingly, we show initiation of human barrier regionally as early as 20-24 wk gestational age (22-26 wk menstrual age), bringing barrier formation close to the time of periderm disaggregation. We use the mouse model to show that patterns of periderm disaggregation mirrors barrier formation. Periderm disaggregation follows and recapitulates barrier pattern, suggesting a relationship between the processes. This work reveals regional patterning in skin maturation and barrier formation in the human infant and demonstrates that initiation of human skin barrier formation in utero coincides with the current lower limit of viability of the pre-term infant.


Subject(s)
Fetus/metabolism , Skin/embryology , Skin/metabolism , Animals , Female , Gestational Age , Humans , Mice , Mice, Inbred ICR , Permeability , Pregnancy , Rabbits , Rats , Rats, Sprague-Dawley
10.
J Agric Food Chem ; 47(9): 3617-27, 1999 Sep.
Article in English | MEDLINE | ID: mdl-10552694

ABSTRACT

Dilute solutions of beta-lactoglobulin (beta-Lg) A, B, and C were heated at temperatures between about 40 and 94 degrees C for 10 min, cooled, and analyzed using Trp fluorescence and extrinsic fluorescence spectra of the probe 1,8-anilinonaphthalene sulfonate (ANS). Thiol availabilities using 5,5'-dithiobis(2-nitrobenzoic acid) (DTNB) were determined using a separate set of samples. The normalized ANS fluorescence emission intensity and the thiol availability results showed a 1:1 relationship with the loss of nativelike but not SDS-monomeric protein, as determined by PAGE analysis. The normalized Trp emission intensity results did not show a comparable 1:1 relationship with the loss of nativelike protein, indicating that the Trp intensity arose from consequential disulfide bond reorganization and not the initial unfolding reaction. The results were also analyzed in terms of two-state models, and the midpoint temperatures (T(mid)) for the proteins were generally beta-Lg C > beta-Lg A > beta-Lg B, and the slopes at the midpoint temperatures for the A variant were generally less than those for the B and C variants indicating that beta-Lg A may denature by a different mechanism from that of beta-Lg B or beta-Lg C. The T(mid) parameters derived from the ANS fluorescence intensity results were similar to those for thiol availability and both were lower than the T(mid) values for Trp emission intensity showing that creation of an ANS binding site on a beta-Lg molecule was linked to the irreversible exposure of a thiol group and the loss of native beta-Lg but preceded the decrease in Trp(61) fluorescence quenching. These results for the differences between the behavior of the A and B or the C variants involved the creation of a destabilizing cavity by the Val(118)Ala (A --> B) substitution and the changed charge distribution within the CD loop caused by the Asp(64)Gly (A --> B) substitution.


Subject(s)
Lactoglobulins/chemistry , Animals , Cattle , Dithionitrobenzoic Acid , Hot Temperature , Protein Isoforms/chemistry , Spectrometry, Fluorescence/methods , Sulfhydryl Compounds/analysis , Thermodynamics
11.
Development ; 125(8): 1541-52, 1998 Apr.
Article in English | MEDLINE | ID: mdl-9502735

ABSTRACT

Skin barrier function is conferred by the outer layer of epidermis, the stratum corneum, and is essential for terrestrial life. Quantitative trans-epidermal water loss assays show that barrier forms late in embryogenesis, permitting the foetus to survive a terrestrial environment at birth. Using qualitative in situ assays for skin permeability, we show that barrier forms in a patterned manner late in mouse gestation. Barrier forms at specific epidermal sites, then spreads around the embryo as a moving front. The moving front of permeability change is accompanied by multiple changes in the outer, stratum corneum-precursor cells. We use the permeability assays to show that final stages of cornified envelope assembly are coordinated with initial stages of barrier formation. Hence the whole-mount permeability assays record developmental acquisition of a known, essential component of the adult barrier. We demonstrate the authenticity of the whole-mount assays after maternal glucocorticoid therapy (known to accelerate barrier formation) and in additional species including the rat where barrier formation is well characterized by TEWL assay (Aszterbaum, M., Menon, G. K., Feingold, K. R. and Williams, M. L. Pediatr. Res. 31, 308-317). The demonstration of patterned barrier formation in other species suggests patterned change as the universal mode of embryonic barrier acquisition. These results highlight the importance of patterning as a mode of epidermal maturation during development.


Subject(s)
Betamethasone/pharmacokinetics , Body Patterning/physiology , Embryonic and Fetal Development , Epidermis/embryology , Skin Physiological Phenomena , Skin/embryology , Animals , Epidermal Cells , Epidermis/growth & development , Female , Filaggrin Proteins , Gestational Age , Intermediate Filament Proteins/biosynthesis , Maternal-Fetal Exchange , Mice , Mice, Inbred ICR , Permeability , Pregnancy , Rats , Skin/cytology , Skin/growth & development , Species Specificity
12.
Appl Environ Microbiol ; 61(1): 310-6, 1995 Jan.
Article in English | MEDLINE | ID: mdl-16534912

ABSTRACT

l-Arginine, an amino acid found in significant quantities in grape juice and wine, is known to be catabolized by some wine lactic acid bacteria. The correlation between the occurrence of arginine deiminase pathway enzymes and the ability to catabolize arginine was examined in this study. The activities of the three arginine deiminase pathway enzymes, arginine deiminase, ornithine transcarbamylase, and carbamate kinase, were measured in cell extracts of 35 strains of wine lactic acid bacteria. These enzymes were present in all heterofermentative lactobacilli and most leuconostocs but were absent in all the homofermentative lactobacilli and pediococci examined. There was a good correlation among arginine degradation, formation of ammonia and citrulline, and the occurrence of arginine deiminase pathway enzymes. Urea was not detected during arginine degradation, suggesting that the catabolism of arginine did not proceed via the arginase-catalyzed reaction, as has been suggested in some earlier studies. Detection of ammonia with Nessler's reagent was shown to be a simple, rapid test to assess the ability of wine lactic acid bacteria to degrade arginine, although in media containing relatively high concentrations (>0.5%) of fructose, ammonia formation is inhibited.

15.
J Mol Biol ; 241(2): 263-4, 1994 Aug 12.
Article in English | MEDLINE | ID: mdl-8057364

ABSTRACT

The cytosolic (Class 1) aldehyde dehydrogenase (AlDH) from sheep liver has been crystallized in a form suitable for X-ray diffraction studies. The crystals, grown by vapour diffusion using 6.5 to 7.5% methoxypolyethylene glycol 5000 as precipitant, at pH 6.5, are orthorhombic with cell dimensions a = 80.7, b = 92.5, c = 151.6 A, space-group P2(1)2(1)2(1), and one dimer in the asymmetric unit. The crystals diffract to at least 2.8 A resolution. Although unmodified AlDH crystallized readily, a key factor in obtaining diffraction-quality crystals was the covalent attachment of an active site reporter group, provided by 3,4-dihydro-3-methyl-6-nitro-2H-1,3-benzoxazin-2-one.


Subject(s)
Aldehyde Dehydrogenase/chemistry , Liver/enzymology , Animals , Crystallization , Crystallography, X-Ray , Cytosol/enzymology , Isoenzymes/chemistry , Sheep
16.
Eur J Biochem ; 205(2): 715-20, 1992 Apr 15.
Article in English | MEDLINE | ID: mdl-1572370

ABSTRACT

The reduction of gluconolactone by glucose-fructose oxidoreductase containing tightly bound NADPH (enzyme-NADPH) is biphasic in nucleotide fluorescence. The initial rapid decrease, which represents quenching of the fluorescence by bound lactone, is followed by a slower decrease which corresponds to the change in absorbance. At low glucose concentrations, the oxidation of glucose by enzyme-NADP+ involves a single first-order process with similar rate constants in fluorescence and absorbance. At higher glucose concentrations, the apparent first-order rate constants for the fluorescence change are less than those for the absorbance change. This is consistent with a mechanism in which the fluorescence change occurs during the lactone dissociation step, which is slower than the hydrogen transfer step during which the absorbance change occurs. The rate constant for gluconolactone dissociation is 360 +/- 10 s-1 and this step is therefore rate-determining for the overall reaction. Reduction of fructose by enzyme-NADPH is first order with a limiting rate constant of at least 2000 s-1.


Subject(s)
Carbohydrate Dehydrogenases/metabolism , Gram-Negative Facultatively Anaerobic Rods/enzymology , NADP/metabolism , Gluconates/metabolism , Kinetics , Lactones , Mathematics , Oxidation-Reduction , Protein Binding , Spectrometry, Fluorescence , Time Factors
17.
Anal Biochem ; 200(1): 171-5, 1992 Jan.
Article in English | MEDLINE | ID: mdl-1595891

ABSTRACT

Isolated rat hepatocytes are used in many metabolic studies, but the viability of these cell preparations is often not adequately established. The present study shows that ATP content is a more reliable index of metabolic viability than trypan blue exclusion. At some of the low trypan blue exclusion levels quoted in the literature, a high percentage of cell preparations is likely to be nonviable by the criterion of ATP content. We suggest that ATP content measured on initial cell preparations and at the end of all incubation procedures is essential for establishing cell viability for metabolic studies on isolated hepatocytes.


Subject(s)
Liver/metabolism , Adenosine Triphosphate/metabolism , Animals , Cells, Cultured , Liver/cytology , Male , Oxygen/metabolism , Rats , Rats, Inbred Strains , Trypan Blue/metabolism
18.
Arch Biochem Biophys ; 290(1): 191-6, 1991 Oct.
Article in English | MEDLINE | ID: mdl-1898089

ABSTRACT

Malate dehydrogenase was purified from the mitochondrial fraction of rat liver by ion-exchange chromatography with affinity elution. The kinetic parameters for the enzyme were determined at pH 7.4 and 37 degrees C, yielding the following values (microM): Ka, 72; Kia, 11; Kb, 110; Kp, 1600; Kip, 7100; Kq, 170; Kiq, 1100, where a = NADH, b = oxalacetate, p = malate, and q = NAD+. Kib was estimated to be about 100 microM. The maximum velocities for mitochondrial malate dehydrogenase in rat liver homogenates, at pH 7.4 and 37 degrees C, were 380 +/- 40 mumol/min per gram of liver, wet weight, for oxalacetate reduction and 39 +/- 3 mumol/min per gram of liver, wet weight, for malate oxidation. Rates of the reaction catalyzed by mitochondrial malate dehydrogenase under conditions similar to those in vivo were calculated using these kinetic parameters and were much lower than the maximum velocity of the enzyme. Since mitochondrial malate dehydrogenase is not saturated with malate at physiological concentrations, its kinetic parameters are probably important in the regulation of mitochondrial malate concentration during ethanol metabolism. For the mitochondrial enzyme to operate at a rate comparable to the flux through cytosolic malate dehydrogenase during ethanol metabolism (about 4 mumol min-1 per gram liver), the mitochondrial [malate] would need to be about 2 mM and the mitochondrial [oxalacetate] would need to be less than 1 microM.


Subject(s)
Ethanol/metabolism , Malate Dehydrogenase/metabolism , Mitochondria, Liver/metabolism , Animals , In Vitro Techniques , Isoelectric Point , Kinetics , Malate Dehydrogenase/isolation & purification , Male , NAD/metabolism , Rats , Rats, Inbred Strains
19.
Biochem J ; 278 ( Pt 3): 659-65, 1991 Sep 15.
Article in English | MEDLINE | ID: mdl-1898355

ABSTRACT

We used titration with the inhibitors tetramethylene sulphoxide and isobutyramide to assess quantitatively the importance of alcohol dehydrogenase in regulation of ethanol oxidation in rat hepatocytes. In hepatocytes isolated from starved rats the apparent Flux Control Coefficient (calculated assuming a single-substrate irreversible reaction with non-competitive inhibition) of alcohol dehydrogenase is 0.3-0.5. Adjustment of this coefficient to allow for alcohol dehydrogenase being a two-substrate reversible enzyme increases the value by 1.3-1.4-fold. The final value of the Flux Control Coefficient of 0.5-0.7 indicates that alcohol dehydrogenase is a major rate-determining enzyme, but that other factors also have a regulatory role. In hepatocytes from fed rats the Flux Control Coefficient for alcohol dehydrogenase decreases with increasing acetaldehyde concentration. This suggests that, as acetaldehyde concentrations rise, control of the pathway shifts from alcohol dehydrogenase to other enzymes, particularly aldehyde dehydrogenase. There is not a single rate-determining step for the ethanol metabolism pathway and control is shared among several steps.


Subject(s)
Alcohol Dehydrogenase/metabolism , Ethanol/metabolism , Liver/enzymology , Acetaldehyde/metabolism , Alcohol Dehydrogenase/antagonists & inhibitors , Amides/pharmacology , Animals , Food , Kinetics , Male , Mathematics , Oxidation-Reduction , Rats , Rats, Inbred Strains , Starvation/enzymology , Sulfoxides , Thiophenes/pharmacology
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