Use of an “acetaldehyde clamp” in the determination of low-KM aldehyde dehydrogenase activity in H4-II-E-C3 rat hepatoma cells

Alcohol ◽  
2003 ◽  
Vol 31 (1-2) ◽  
pp. 19-24 ◽  
Author(s):  
Claudio Moncada ◽  
Nelson Fuentes ◽  
Alvaro Lladser ◽  
Gonzalo Encina ◽  
Amalia Sapag ◽  
...  
2001 ◽  
Vol 130-132 ◽  
pp. 219-225 ◽  
Author(s):  
Giuliana Muzio ◽  
Rosa Angela Canuto ◽  
Antonella Trombetta ◽  
Marina Maggiora

1992 ◽  
Vol 38 (4) ◽  
pp. 584-588 ◽  
Author(s):  
R D Johnson ◽  
J Bahnisch ◽  
B Stewart ◽  
D J Shearman ◽  
J B Edwards

Abstract We describe a reliable and sensitive semiautomated spectrophotometric assay of aldehyde dehydrogenase (ALDH; EC 1.2.1.3) activity in erythrocytes. The hemolysate can be stabilized with sucrose, and the technique involves only microliters of hemolysate on a centrifugal analyzer. The use of microcolumns to remove interfering hemoglobin is avoided, and reproducibility of the assay has been improved by manipulating the inherent lactate dehydrogenase activity of erythrocytes by adding lactate and oxalate to the reaction mixture. These modifications have decreased the analytical imprecision of the assay, allowing a better appraisal of aldehyde dehydrogenase activity in erythrocytes as a biological marker of excess alcohol consumption. Erythrocytic ALDH activity was significantly less in 40 alcoholics than in 145 teetotallers (median activity 128 vs 219 mU/g of hemoglobin, respectively; P = 0.0001), indicating the potential of this assay as a useful marker of excess alcohol consumption.


2001 ◽  
Vol 357 (3) ◽  
pp. 811-818 ◽  
Author(s):  
Rosa A. CANUTO ◽  
Margherita FERRO ◽  
Raffaella A. SALVO ◽  
Anna M. BASSI ◽  
Antonella TROMBETTA ◽  
...  

Aldehyde dehydrogenase (ALDH) is a family of several isoenzymes important in cell defence against both exogenous and endogenous aldehydes. Compared with normal hepatocytes, in rat hepatoma cells the following changes in the expression of ALDH occur: cytosolic class 3 ALDH expression appears and mitochondrial class 2 ALDH decreases. In parallel with these changes, a decrease in the polyunsaturated fatty acid content in membrane phospholipids occurs. In the present study we demonstrated that restoring the levels of arachidonic acid in 7777 and JM2 rat hepatoma cell lines to those seen in hepatocytes decreases hepatoma cell growth, and increases class 2 ALDH activity. This latter effect appears to be due to an increased gene transcription of class 2 ALDH. To account for this increase, we examined whether peroxisome-proliferator-activated receptors (PPARs) or lipid peroxidation were involved. We demonstrated a stimulation of PPAR expression, which is different in the two hepatoma cell lines: in the 7777 cell line, there was an increase in PPARα expression, whereas PPARγ expression increased in JM2 cells. We also found increased lipid peroxidation, but this increase became evident at a later stage when class 2 ALDH expression had already increased. In conclusion, arachidonic acid added to the culture medium of hepatoma cell lines is able to partially restore the normal phenotype of class 2 ALDH, in addition to a decrease in cell growth.


2001 ◽  
Vol 357 (3) ◽  
pp. 811 ◽  
Author(s):  
Rosa A. CANUTO ◽  
Margherita FERRO ◽  
Raffaella A. SALVO ◽  
Anna M. BASSI ◽  
Antonella TROMBETTA ◽  
...  

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