Although antiarrhythmic drugs are used to treat digitalis-induced cardiac disorders, some of these drugs have been reported to increase the serum digoxin concentration in patients, causing the severe side-effects. We have previously shown that many basic drugs including antiarrhythmic drugs inhibite
A comparison of copper uptake by liver plasma membrane vesicles and uptake by isolated cultured rat hepatocytes
β Scribed by Michelle J. Bingham; Dr. Harry J. McArdle
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 700 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0270-9139
No coin nor oath required. For personal study only.
β¦ Synopsis
We studied copper uptake from copper dihistidine complexes by plasma membrane vesicles isolated from rat liver and compared the data with those for uptake under the same conditions by hepatocytes cultured from rat liver to determine whether membrane vesicles can be used to study copper uptake. Marker enzyme analysis showed a 28-fold increase in 5'-nucleotidase activity, a slight increase in endoplasmic reticulum and no contamination with mitochondrial membranes. Copper uptake by vesicles is temperature dependent, and solubilization with Triton X-100 results in a loss of accumulative capacity. Increasing osmotic pressure resulted in a decrease in copper levels in the vesicles at equilibrium, showing that uptake--as opposed to binding by the vesicles--occurred. Uptake by vesicles is concentration dependent, with evidence for cooperation in the uptake sites. The substrate concentration yielding 10% maximum uptake was 4.01 +/- 0.5 mumol/L, maximum uptake was 10.8 +/- 0.4 nmol/Cu/mg protein.min and the n value was 1.5 +/- 0.2. In contrast, uptake by cells showed no cooperation (n = 1.09 +/- 0.06) and a significantly higher apparent Michaelis-Menten constant (17.4 +/- 1.3 mumol/L). As expected, the maximum uptake was lower in the hepatocytes (1.82 +/- 0.08 nmol/mg protein.min). Albumin, N-ethylmaleimide and zinc all inhibited uptake in vesicles and in hepatocytes, and the degrees of inhibition were similar in both types of preparation. Vitamin C stimulated uptake in both vesicles and hepatocytes; again, there was a correlation between the increase in uptake at different concentrations. However, cadmium inhibited uptake and nickel stimulated uptake in vesicles and neither metal had any effect in hepatocytes.(ABSTRACT TRUNCATED AT 250 WORDS)
π SIMILAR VOLUMES
To differentiate between the "intact" and "sick" cell hypoβ¬he& explaining decreased clearance of endo-and xenobbtics, we meaeured uptake of taurocholate and OIlQBOill in hepatocytes isolated from cirrhotic rat liver. Cirrhouis was induced by chronic exposure of male Sprague-Dawley rats to phenobarbi
Taurocholate (TC) uptake by adult rat hepatocytes co-cultured with other rat liver epithelial cells (RLEC) was studied comparatively to hepatocytes in primary culture. Cells were cultured on Petri dishes for desired times prior to measuring their ability to transport TC. TC uptake was linear for 150
Effect of temperature on alanine uptake by membrane vesicles isolated from a psychrophilic marine bacteriuml) J . A. NOVITSKY~) and
To determine whether phenobarbital affects hepatocellular bilirubinlsulfobromophthalein uptake mechanism, we administered it to male Sprague-Dawley rats, body weight 175 f 25 g m , at doses of 1 to 75 mg/kg body wtiday for 7 days. Control rats were given an equivalent volume of physiological saline