EFFECT OF ADRENOCORTICOTROPHIN ON INTRACELLULAR CHOLESTEROL TRANSPORT

1980 ◽  
Vol 84 (2) ◽  
pp. 179-188 ◽  
Author(s):  
MASAHISA NAKAMURA ◽  
MASAAKI WATANUKI ◽  
B. E. TILLEY ◽  
P. F. HALL

The rate of side-chain cleavage of cholesterol by mitochondria derived from mouse adrenal tumour cells was measured. Incubation of the cells in the presence of adrenocorticotrophin (ACTH) for periods of up to 1 h was without effect on the subsequent side-chain cleavage by mitochondria. However, if the cells were incubated in the presence of aminoglutethimide phosphate (0·76 mmol/l), addition of ACTH (final concentration 86 u./l) to the medium containing the cells increased the subsequent rate of side-chain cleavage by the isolated mitochondria. This response reached a maximum after incubation of cells with ACTH for 2 h and decayed when the isolated mitochondria were left at 0 °C, although a significant difference was still apparent after 120 min. Similar stimulation of mitochondrial side-chain cleavage by ACTH was observed when the reaction was inhibited by anaerobiosis instead of aminoglutethimide phosphate. Addition of dibutyryl cyclic AMP, at final concentrations greater than 10−5 mol/l, to cells during incubation with aminoglutethimide phosphate (0·76 mmol/l) also stimulated the conversion of cholesterol to pregnenolone by the mitochondria. Provided the adrenal tumour cells were incubated with aminoglutethimide, or anaerobically, the mean cholesterol content of the inner mitochondrial membrane was significantly higher (P < 0·01) when ACTH was included in the incubation medium than when it was not. It is concluded that ACTH increases the movement of cholesterol to the mitochondrial membrane which contains the side-chain cleavage enzyme system and that part of this cholesterol is used for the enhanced conversion of cholesterol to pregnenolone brought about by ACTH.

1986 ◽  
Vol 108 (3) ◽  
pp. 377-384 ◽  
Author(s):  
F. Lambert ◽  
J. Lammerant ◽  
J. Kolanowski

ABSTRACT The postulated prolonged stimulatory influence of ACTH on the adrenocortical mitochondrial synthesis of pregnenolone in response to ACTH was studied in adrenal mitochondria isolated from control guinea-pigs and from animals treated s.c. with 100 μg ACTH(1–24) twice daily on the day before the animals were killed. The animals from both groups were injected with 100 μg ACTH s.c. 30 min before killing. The mitochondrial production of pregnenolone (expressed in nmol per mg mitochondrial protein after 10-min incubation) increased from 1·52 ± 0·46 (s.e.m.) in the control group to 4·50 ± 0·59 for mitochondria from ACTH-treated animals, despite a similar free cholesterol content in the mitochondria, even when determined after a previous in-vivo treatment with aminoglutethimide to block further metabolism of cholesterol into pregnenolone. In addition, in the presence of an excess of exogenous cholesterol (100 μmol/l), the production of pregnenolone remained higher for mitochondria from ACTH-treated animals. In contrast, when the calcium concentration in the incubation medium was raised to 1 mmol/l, with subsequent enhancement in pregnenolone synthesis, the mitochondrial pregnenolone production became similar for both groups (8·28 ± 1·11 nmol in the ACTH-treated group and 9·55 ± 1·90 nmol in the control group), even in the presence of 100 μmol cholesterol/l (13·5 ±1·80 nmol in ACTH-treated animals and 14·8 ± 1·93 nmol in controls). Cycloheximide treatment administered on the day before the animals were killed was without any effect on pregnenolone production in control animals (3·51 ± 0·43 nmol before and 3·65 ± 0·63 nmol after cycloheximide treatment). In contrast, the pregnenolone production by mitochondria from ACTH-treated guinea-pigs injected with cycloheximide was reduced to a level similar to that observed in the control group (5·82± 0·23 nmol in the absence and 3·09± 0·32nmol in the presence of cycloheximide treatment). The results of the present study suggest that the prolonged stimulatory effect of ACTH on pregnenolone production involves an increase in the synthesis of a protein factor which promotes the availability of cholesterol to the side-chain cleavage system. Other mechanisms such as a stimulated synthesis of the side-chain cleavage complex itself or an increased total mitochondrial cholesterol content are not supported by our data. J. Endocr. (1986) 108, 377–384


2013 ◽  
pp. 1-1
Author(s):  
Alisdair Boag ◽  
Kerry McLaughlin ◽  
Mike Christie ◽  
Peter Graham ◽  
Harriet Syme ◽  
...  

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