Dutta H, Sengupta M, Pal D K, De A U, Sengupta C
Department of Pharmaceutical Technology, Jadavpur University, Calcutta.
Indian J Biochem Biophys. 1993 Apr;30(2):128-32.
Considering the high lipophilicity of propranolol (log P = 3.56), its interactions with the cell membrane lipids of goat blood have been investigated. It is observed that lipid loss after incubation of blood cells with propranolol hydrochloride in salt glucose medium for varying periods of time was accompanied with significant increases in PUFAs. Amongst the PUFAs studied the omega 3 and omega 6 fatty acids, the two important precursors of eicosenoids, have shown increase in varying amounts. This phenomenon is presumably responsible for the significant cardiovascular activity of this drug.
考虑到普萘洛尔的高亲脂性(log P = 3.56),已对其与山羊血液细胞膜脂质的相互作用进行了研究。观察到,在盐葡萄糖培养基中,血细胞与盐酸普萘洛尔孵育不同时间后脂质损失,同时多不饱和脂肪酸显著增加。在所研究的多不饱和脂肪酸中,二十碳类化合物的两个重要前体ω-3和ω-6脂肪酸呈现出不同程度的增加。这种现象可能是该药物具有显著心血管活性的原因。