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Alcohol Dehydrogenase Activities (alcohol + dehydrogenase_activity)

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Chemistry25%

Selected Abstracts

Chronic Ethanol Consumption Results in Atypical Liver Injury in Copper/Zinc Superoxide Dismutase Deficient Mice

ALCOHOLISM, Issue 2 2010
Tiana V. Curry-McCoy
Background:, Ethanol metabolism increases production of reactive oxygen species, including superoxide () in the liver, resulting in significant oxidative stress, which causes cellular damage. Superoxide dismutase (SOD) is an antioxidant enzyme that converts superoxide to less toxic intermediates, preventing accumulation. Because the absence of SOD would confer less resistance to oxidative stress, we determined whether damage to hepatic proteolytic systems was greater in SOD,/, than in SOD+/+ mice after chronic ethanol feeding. Methods:, Female wild-type (SOD+/+) and Cu/Zn-SOD knockout (SOD,/,) mice were pair-fed ethanol and control liquid diets for 24 days, after which liver injury was assessed. Results:, Ethanol-fed SOD,/, mice had 4-fold higher blood ethanol, 2.8-fold higher alanine aminotransferase levels, 20% higher liver weight, a 1.4-fold rise in hepatic protein levels, and 35 to 70% higher levels of lipid peroxides than corresponding wild-type mice. While wild-type mice exhibited fatty liver after ethanol administration, SOD,/, mice showed no evidence of ethanol-induced steatosis, although triglyceride levels were elevated in both groups of knockout mice. Ethanol administration caused no significant change in proteasome activity, but caused lysosomal leakage in livers of SOD,/, mice but not in wild-type mice. Alcohol dehydrogenase activity was reduced by 50 to 60% in ethanol-fed SOD,/, mice compared with all other groups. Additionally, while ethanol administration induced cytochrome P450 2E1 (CYP2E1) activity in wild-type mice, it caused no such induction in SOD,/, mice. Unexpectedly, ethanol feeding significantly elevated total and mitochondrial levels of glutathione in SOD knockout mice compared with wild-type mice. Conclusion:, Ethanol-fed SOD,/, mice exhibited lower alcohol dehydrogenase activity and lack of CYP2E1 inducibility, thereby causing decreased ethanol metabolism compared with wild-type mice. These and other atypical responses to ethanol, including the absence of ethanol-induced steatosis and enhanced glutathione levels, appear to be linked to enhanced oxidative stress due to lack of antioxidant enzyme capacity. [source]

,Defence lignin' and hydroxycinnamyl alcohol dehydrogenase activities in wounded Eucalyptus gunnii

FOREST PATHOLOGY, Issue 2 2003
S. Hawkins
Summary To learn more about lignin formation in response to wounding in trees, we adopted two complementary approaches: (1) microscopic and histochemical studies of the wound response in 3.5-month-old Eucalyptus gunnii plantlets and (2) biochemical investigations of hydroxycinnamyl alcohol dehydrogenase activities in wounded 6-year-old, field-grown E. gunnii trees. The first approach revealed that a barrier zone was formed in response to wounding in both ground tissues (cortex barrier and pith reaction zone) and vascular tissues. The barrier zone was barely detectable after 24 h but well-developed 7 days after wounding. Microscopic analyses indicated that the barrier zone was formed by the reinforcement of cell walls with ,lignin-like material' in both ground tissues and vascular tissue, and that, in addition, the lumen of certain xylem cells (vessels and fibres) were blocked by the deposition of polymeric phenolic material. Histochemical characterization revealed that the lignin-like material (,defence lignin') deposited in ground tissue cell walls and xylem cell blockages was poor in syringyl (S-type) lignin units and therefore differed from the usual mixed guaiacyl,syringyl (G,S) lignin unit composition of E. gunnii developmental lignin. In contrast, S-type lignin appeared to be deposited in the cell walls of immature developing secondary xylem cells at a stage when the cell walls of comparable cells from unwounded control stems contained lignin poor in syringyl units. The second approach indicated that two different types of cinnamyl alcohol dehydrogenase activity are induced, and apparently regulated differentially, in response to wounding in E. gunnii trees. Coniferyl alcohol dehydrogenase activity was induced immediately and continued to increase throughout the first 15 days of the 17-day experimental period, while sinapyl alcohol dehydrogenase activity was first detected at 8 days after wounding and continued to increase throughout the experimental period. The biological roles of the two alcohol dehydrogenase activities are discussed in relation to the formation of defence lignin versus developmental lignin in trees. Résumé Afin d'approfondir nos connaissances concernant la formation de lignine en réponse aux blessures chez les arbres, nous avons utilisé deux approches complémentaires: (1) des études microscopiques et histochimiques de la réponse à la blessure chez les plantules d'Eucalyptus gunniiâgées de 3 mois et demi, et (2) des analyses biochimiques des activités alcools hydroxycinnamyliques déshydrogénases chez les arbres âgés de 6 ans blessés au champ. L'utilization de la première approche a révélé qu'une barrière physique se forme en réponse à la blessure aux niveaux des tissus vasculaires, de la moelle, et des tissus externes au phloème. A 24 h après la blessure, cette barrière est peu développée mais elle est bien formée après 7 jours. Les analyses microscopiques et histochimiques ont indiqué que les parois cellulaires au niveau de la barrière sont renforcées par un composé semblable à la lignine (,lignin-like material'). De plus, les lumens de plusieurs cellules xylémiennes (vaisseaux et fibres) sont bouchées par le dépôt d'un composé polymérique de nature phénolique. Les caractérizations histochimiques ont indiqué que le ,lignin-like material' (lignine de défense) déposé dans les parois cellulaires de la moelle et des tissus externes au phloème, et dans les lumens des cellules xylemiennes, contient peu d'unités syringyles (type-S). En conséquence, cette ,lignine de défense' se distingue de la ,lignine de développement' typique d'E. gunnii, qui est composée d'unités guaiacyles (type-G) et d'unités syringyles (type-S). En revanche chez les plantules blessées, des unités syringyles sont déposées dans les parois des cellules immatures du xylème à un stade où les cellules comparables des plantules témoins ne contiennent que très peu d'unités syringyles. La deuxième approche a indiqué que deux activités alcools cinnamyliques déshydrogénases différentes sont induites, et régulées d'une façon différencielle, en réponse à la blessure chez les arbres d'E. gunnii. L'activité alcool coniférylique déshydrogénase est induite rapidement et continue d'augmenter pendant les 15 premiers jours de la période expérimentale de 17 jours, tandis que l'activité alcool sinapylique déshydrogénase est seulement détectée à 8 jours après la blessure et continue d'augmenter le long de la période expérimentale. Les rôles biologiques potentiels de ces deux activités alcools déshydrogénases sont discutés en relation avec la formation de la lignine de défense et avec la lignine de développement chez les arbres. Zusammenfassung Zur Untersuchung der Ligninbildung nach Verletzungen bei Bäumen wurden zwei sich ergänzende Forschungsansätze gewählt: 1. Mikroskopische und histochemische Untersuchungen der Wundreaktion an Jungpflanzen (3,5 Monate alt) von Eucalyptus gunnii und 2. Biochemische Untersuchungen der Hydroxycinnamylalkohol-Dehydrogenase-Aktivität bei verletzten, sechs Jahre alten E. gunnii -Bäumen im Freiland. Der erste Ansatz zeigte, dass eine Barrierezone als Antwort auf die Verletzung sowohl in beiden Grundgeweben (Cortex-Barriere und Reaktionszone im Mark) als auch in den Leitgeweben gebildet wird. Die Barrierezone war 24 Stunden nach der Verletzung gerade erkennbar, nach sieben Tagen war sie gut entwickelt. Die mikroskopische Untersuchung zeigte, dass die Barrierezone durch Verstärkung der Zellwände mit ,,ligninartigem Material,, im Grund- und Leitgewebe gebildet wurde, und dass zusätzlich das Lumen gewisser Xylemzellen (Gefässe und Fasern) durch Ablagerung von polymerem phenolischem Material verschlossen wurde. Die histochemische Analyse ergab, dass das ligninartige Material (,,Abwehrlignin,,), das in den Zellwänden des Grundgewebes und in den Lumina der Xylemzellen abgelagert wurde, geringe Mengen an Syringyl-(S-Typ)-Lignineinheiten enthielt und sich somit von der normalen Guaiacyl-Syringyl(G-S)-Komposition des Lignins von E. gunnii unterschied. Das S-Typ-Lignin wurde offenbar in den Zellwänden sich entwickelnder sekundärer Xylemzellen abgelagert. Diese Einlagerung erfolgte in einem Stadium, in dem die Zellwände der vergleichbaren Zellen in unverletzten Kontrollstämmen Lignin mit geringem Syringylgehalt enthielten. Der zweite Versuchsansatz zeigte, dass als Reaktion auf die Verletzung zwei verschiedene Arten von Cinnamylalkohol-Dehydrogenase-Aktivitäten induziert und offensichtlich unterschiedlich reguliert werden. Die Aktivität der Coniferyl-Alkohol-Dehydrogenase wurde sofort induziert und sie nahm während 15 Tagen der 17tägigen Versuchsperiode stetig zu, während die Aktivität der Sinapyl-Dehydrogenase erstmals 8 Tage nach der Verletzung nachweisbar war und dann während der gesamten Versuchsperiode anstieg. Die biologische Bedeutung der beiden Alkoholdehydrogenase-Aktivitäten werden in Bezug auf die Bildung von Abwehr-Lignin im Vergleich zur normalen Ligninbildung in Bäumen diskutiert. [source]

Ethanol-induced alterations of the antioxidant defense system in rat kidney

JOURNAL OF BIOCHEMICAL AND MOLECULAR TOXICOLOGY, Issue 6 2006
Diana Dinu
Abstract We report here the effects of chronic ethanol consumption on the antioxidant defense system in rat kidney. Thirty-two male Wistar rats were randomly divided in two identical groups and were treated as follows: control group (water for fluid) and the ethanol-fed group (2 g/kg body weight/24 h). The animals were sacrificed after 10 weeks, and respectively 30 weeks of ethanol consumption, and the renal tissue was isolated and analyzed. Results revealed that kidney alcohol dehydrogenase activities increased significantly after ethanol administration, but the electrophoretic pattern of alcohol dehydrogenase isoforms was unmodified. The SDS polyacrylamidegel electrophoretic study of kidney proteins has revealed the appearance of two new protein bands after long-term ethanol consumption. The kidney reduced glutathione/oxidized glutathione ratio decreased, indicating an oxidative stress response due to ethanol ingestion. The malondialdehyde contents and xanthine oxidase activities were unchanged. The antioxidant enzymatic defense system showed a different response during the two periods of ethanol administration. After 10 weeks, catalase, glutathione peroxidase, glutathione reductase, and glucose-6-phosphate dehydrogenase were activated, while superoxide dismutase, glutathione transferase, and ,-glutamyltranspeptidase levels were stationary. After 30 weeks, superoxide dismutase and glutathione peroxidase activities were unmodified, but catalase, glutathione transferase, ,-glutamyltranspeptidase, glutathione reductase, and glucose-6-phosphate dehydrogenase activities were significantly increased. Remarkable changes have been registered after 30 weeks of ethanol administration for glutathione reductase and glucose-6-phosphate dehydrogenase activities, including an increase by 106 and 216' of control values, respectively. These results showed specific changes in rat kidney antioxidant system and glutathione status as a consequence of long-term ethanol administration. © 2005 Wiley Periodicals, Inc. J Biochem Mol Toxicol 19:386-395, 2005; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/jbt.20101 [source]

Influence of postharvest water stress on lipoxygenase and alcohol dehydrogenase activities, and on the composition of some volatile compounds of Gewürztraminer grapes dehydrated under controlled and uncontrolled thermohygrometric conditions

AUSTRALIAN JOURNAL OF GRAPE AND WINE RESEARCH, Issue 3 2007
L. CHKAIBAN
ABSTRACT Gewürztraminer grapes with a sugar content of around 212 g/L (21.7oBrix) were dried at 17oC, 40% relative humidity and 1.5 m/sec air flow in a 300 L thermo-conditioned tunnel. Control grapes were dried traditionally in a window ventilated room, under uncontrolled environmental conditions varying with outside climate. Tunnel-dried grapes reached the desired sugar concentration (305 g/L, 29.5oBrix) in 17 days, loosing 36% of their weight. Control grapes lost only 22% of their weight and grey mould developed in several bunches at the last sampling. Titratable acidity decreased for tunnel-dried and control grapes from 6.5 g/L to 4 g/L and 5 g/L, respectively. Lipoxygenase (LOX) activity declined in both samples from 120 to 90 U/mg protein dw, with a subsequent significant increase after 20% weight loss in tunnel-treated grapes while the control grapes showed a small peak (150 U/mg protein dw) at 13% weight loss. Six carbon compound evolution showed a loose correlation with LOX activity. Alcohol dehydrogenase specific activity and the concentrations of ethanol and of acetaldehyde plus ethyl acetate showed fluctuating patterns of change, with the evolution of these three variables showing similarity, particularly evident in the tunnel-dried grapes. Carotenoids declined significantly, to increase slightly at the end of the experiment in both samples, with the decline more rapid in the control grapes. Traditional, uncontrolled conditions, did not permit constant dehydration, and provoked a rapid stress to the berries (10% of weight loss). Controlled conditions permitted uniform dehydration, postponed water stress, giving a higher quality product without loss of berries. [source]

,Defence lignin' and hydroxycinnamyl alcohol dehydrogenase activities in wounded Eucalyptus gunnii

FOREST PATHOLOGY, Issue 2 2003
S. Hawkins
Summary To learn more about lignin formation in response to wounding in trees, we adopted two complementary approaches: (1) microscopic and histochemical studies of the wound response in 3.5-month-old Eucalyptus gunnii plantlets and (2) biochemical investigations of hydroxycinnamyl alcohol dehydrogenase activities in wounded 6-year-old, field-grown E. gunnii trees. The first approach revealed that a barrier zone was formed in response to wounding in both ground tissues (cortex barrier and pith reaction zone) and vascular tissues. The barrier zone was barely detectable after 24 h but well-developed 7 days after wounding. Microscopic analyses indicated that the barrier zone was formed by the reinforcement of cell walls with ,lignin-like material' in both ground tissues and vascular tissue, and that, in addition, the lumen of certain xylem cells (vessels and fibres) were blocked by the deposition of polymeric phenolic material. Histochemical characterization revealed that the lignin-like material (,defence lignin') deposited in ground tissue cell walls and xylem cell blockages was poor in syringyl (S-type) lignin units and therefore differed from the usual mixed guaiacyl,syringyl (G,S) lignin unit composition of E. gunnii developmental lignin. In contrast, S-type lignin appeared to be deposited in the cell walls of immature developing secondary xylem cells at a stage when the cell walls of comparable cells from unwounded control stems contained lignin poor in syringyl units. The second approach indicated that two different types of cinnamyl alcohol dehydrogenase activity are induced, and apparently regulated differentially, in response to wounding in E. gunnii trees. Coniferyl alcohol dehydrogenase activity was induced immediately and continued to increase throughout the first 15 days of the 17-day experimental period, while sinapyl alcohol dehydrogenase activity was first detected at 8 days after wounding and continued to increase throughout the experimental period. The biological roles of the two alcohol dehydrogenase activities are discussed in relation to the formation of defence lignin versus developmental lignin in trees. Résumé Afin d'approfondir nos connaissances concernant la formation de lignine en réponse aux blessures chez les arbres, nous avons utilisé deux approches complémentaires: (1) des études microscopiques et histochimiques de la réponse à la blessure chez les plantules d'Eucalyptus gunniiâgées de 3 mois et demi, et (2) des analyses biochimiques des activités alcools hydroxycinnamyliques déshydrogénases chez les arbres âgés de 6 ans blessés au champ. L'utilization de la première approche a révélé qu'une barrière physique se forme en réponse à la blessure aux niveaux des tissus vasculaires, de la moelle, et des tissus externes au phloème. A 24 h après la blessure, cette barrière est peu développée mais elle est bien formée après 7 jours. Les analyses microscopiques et histochimiques ont indiqué que les parois cellulaires au niveau de la barrière sont renforcées par un composé semblable à la lignine (,lignin-like material'). De plus, les lumens de plusieurs cellules xylémiennes (vaisseaux et fibres) sont bouchées par le dépôt d'un composé polymérique de nature phénolique. Les caractérizations histochimiques ont indiqué que le ,lignin-like material' (lignine de défense) déposé dans les parois cellulaires de la moelle et des tissus externes au phloème, et dans les lumens des cellules xylemiennes, contient peu d'unités syringyles (type-S). En conséquence, cette ,lignine de défense' se distingue de la ,lignine de développement' typique d'E. gunnii, qui est composée d'unités guaiacyles (type-G) et d'unités syringyles (type-S). En revanche chez les plantules blessées, des unités syringyles sont déposées dans les parois des cellules immatures du xylème à un stade où les cellules comparables des plantules témoins ne contiennent que très peu d'unités syringyles. La deuxième approche a indiqué que deux activités alcools cinnamyliques déshydrogénases différentes sont induites, et régulées d'une façon différencielle, en réponse à la blessure chez les arbres d'E. gunnii. L'activité alcool coniférylique déshydrogénase est induite rapidement et continue d'augmenter pendant les 15 premiers jours de la période expérimentale de 17 jours, tandis que l'activité alcool sinapylique déshydrogénase est seulement détectée à 8 jours après la blessure et continue d'augmenter le long de la période expérimentale. Les rôles biologiques potentiels de ces deux activités alcools déshydrogénases sont discutés en relation avec la formation de la lignine de défense et avec la lignine de développement chez les arbres. Zusammenfassung Zur Untersuchung der Ligninbildung nach Verletzungen bei Bäumen wurden zwei sich ergänzende Forschungsansätze gewählt: 1. Mikroskopische und histochemische Untersuchungen der Wundreaktion an Jungpflanzen (3,5 Monate alt) von Eucalyptus gunnii und 2. Biochemische Untersuchungen der Hydroxycinnamylalkohol-Dehydrogenase-Aktivität bei verletzten, sechs Jahre alten E. gunnii -Bäumen im Freiland. Der erste Ansatz zeigte, dass eine Barrierezone als Antwort auf die Verletzung sowohl in beiden Grundgeweben (Cortex-Barriere und Reaktionszone im Mark) als auch in den Leitgeweben gebildet wird. Die Barrierezone war 24 Stunden nach der Verletzung gerade erkennbar, nach sieben Tagen war sie gut entwickelt. Die mikroskopische Untersuchung zeigte, dass die Barrierezone durch Verstärkung der Zellwände mit ,,ligninartigem Material,, im Grund- und Leitgewebe gebildet wurde, und dass zusätzlich das Lumen gewisser Xylemzellen (Gefässe und Fasern) durch Ablagerung von polymerem phenolischem Material verschlossen wurde. Die histochemische Analyse ergab, dass das ligninartige Material (,,Abwehrlignin,,), das in den Zellwänden des Grundgewebes und in den Lumina der Xylemzellen abgelagert wurde, geringe Mengen an Syringyl-(S-Typ)-Lignineinheiten enthielt und sich somit von der normalen Guaiacyl-Syringyl(G-S)-Komposition des Lignins von E. gunnii unterschied. Das S-Typ-Lignin wurde offenbar in den Zellwänden sich entwickelnder sekundärer Xylemzellen abgelagert. Diese Einlagerung erfolgte in einem Stadium, in dem die Zellwände der vergleichbaren Zellen in unverletzten Kontrollstämmen Lignin mit geringem Syringylgehalt enthielten. Der zweite Versuchsansatz zeigte, dass als Reaktion auf die Verletzung zwei verschiedene Arten von Cinnamylalkohol-Dehydrogenase-Aktivitäten induziert und offensichtlich unterschiedlich reguliert werden. Die Aktivität der Coniferyl-Alkohol-Dehydrogenase wurde sofort induziert und sie nahm während 15 Tagen der 17tägigen Versuchsperiode stetig zu, während die Aktivität der Sinapyl-Dehydrogenase erstmals 8 Tage nach der Verletzung nachweisbar war und dann während der gesamten Versuchsperiode anstieg. Die biologische Bedeutung der beiden Alkoholdehydrogenase-Aktivitäten werden in Bezug auf die Bildung von Abwehr-Lignin im Vergleich zur normalen Ligninbildung in Bäumen diskutiert. [source]

Chronic Ethanol Consumption Results in Atypical Liver Injury in Copper/Zinc Superoxide Dismutase Deficient Mice

ALCOHOLISM, Issue 2 2010
Tiana V. Curry-McCoy
Background:, Ethanol metabolism increases production of reactive oxygen species, including superoxide () in the liver, resulting in significant oxidative stress, which causes cellular damage. Superoxide dismutase (SOD) is an antioxidant enzyme that converts superoxide to less toxic intermediates, preventing accumulation. Because the absence of SOD would confer less resistance to oxidative stress, we determined whether damage to hepatic proteolytic systems was greater in SOD,/, than in SOD+/+ mice after chronic ethanol feeding. Methods:, Female wild-type (SOD+/+) and Cu/Zn-SOD knockout (SOD,/,) mice were pair-fed ethanol and control liquid diets for 24 days, after which liver injury was assessed. Results:, Ethanol-fed SOD,/, mice had 4-fold higher blood ethanol, 2.8-fold higher alanine aminotransferase levels, 20% higher liver weight, a 1.4-fold rise in hepatic protein levels, and 35 to 70% higher levels of lipid peroxides than corresponding wild-type mice. While wild-type mice exhibited fatty liver after ethanol administration, SOD,/, mice showed no evidence of ethanol-induced steatosis, although triglyceride levels were elevated in both groups of knockout mice. Ethanol administration caused no significant change in proteasome activity, but caused lysosomal leakage in livers of SOD,/, mice but not in wild-type mice. Alcohol dehydrogenase activity was reduced by 50 to 60% in ethanol-fed SOD,/, mice compared with all other groups. Additionally, while ethanol administration induced cytochrome P450 2E1 (CYP2E1) activity in wild-type mice, it caused no such induction in SOD,/, mice. Unexpectedly, ethanol feeding significantly elevated total and mitochondrial levels of glutathione in SOD knockout mice compared with wild-type mice. Conclusion:, Ethanol-fed SOD,/, mice exhibited lower alcohol dehydrogenase activity and lack of CYP2E1 inducibility, thereby causing decreased ethanol metabolism compared with wild-type mice. These and other atypical responses to ethanol, including the absence of ethanol-induced steatosis and enhanced glutathione levels, appear to be linked to enhanced oxidative stress due to lack of antioxidant enzyme capacity. [source]