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[二丁酰环磷腺苷、维拉帕米和肾上腺素对巨噬细胞胆固醇动员的影响]

[The effect of dibutyryl cAMP, verapamil and adrenaline on cholesterol mobilization from macrophages].

作者信息

Dushkin M I, Mandrikova E V, Dolgov A V

出版信息

Farmakol Toksikol. 1990 Jul-Aug;53(4):44-6.

PMID:2171980
Abstract

The capacity of dibutyryladenosine-3':5'-cyclic phosphate (dibutyryl cAMP), verapamil and epinephrine to modulate cholesterol (CH) excretion was studied in the stored (4-14C)-CH rat macrophages. The experiments indicated that in the absence of high density lipoproteins (HDL) the addition of dibutyryl cAMP (0.2 mmol), verapamil (0.05 mmol), epinephrine (0.05 mmol) in cultured medium did not influence the excretion of the stored (4-14C)-CH from macrophages during 4, 8 and 18 hours. The addition of the drugs in the presence of HDL resulted in an increase in the excretion of (4-14C)-CH from macrophages during incubation. The data indicate that the drugs which increase the cellular concentration of cAMP can induce the mobilization of CH from macrophages in the presence of acceptors of CH.

摘要

在储存有(4-¹⁴C)-胆固醇的大鼠巨噬细胞中,研究了二丁酰腺苷-3':5'-环磷酸酯(二丁酰环磷腺苷)、维拉帕米和肾上腺素调节胆固醇(CH)排泄的能力。实验表明,在缺乏高密度脂蛋白(HDL)的情况下,在培养基中添加二丁酰环磷腺苷(0.2 mmol)、维拉帕米(0.05 mmol)、肾上腺素(0.05 mmol),在4、8和18小时内均不影响储存的(4-¹⁴C)-胆固醇从巨噬细胞中的排泄。在HDL存在的情况下添加这些药物,会导致孵育期间(4-¹⁴C)-胆固醇从巨噬细胞中的排泄增加。数据表明,在存在胆固醇受体的情况下,能增加细胞内环磷腺苷浓度的药物可诱导巨噬细胞中胆固醇的动员。

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