Coburn R F, Cunningham M, Strauss J F
Biochim Biophys Acta. 1981 Apr 23;664(1):188-99. doi: 10.1016/0005-2760(81)90041-2.
We studied the effects of immersion of guinea-pig taenia coli strips in potassium-free media on arachidonate stores and other lipid fractions. Control studies obtained with the strips in Krebs solution showed that greater than 97% of arachidonate was found esterified in phospholipid with the following distribution: phosphatidylethanolamine greater than phosphatidylcholine greater than phosphatidylserine plus phosphatidylinositol. 30 min incubation of the strips with [3H]arachidonate complexed to albumin resulted in incorporation of this isotope into phospholipid and neutral lipid fractions, phosphatidylcholine greater than neutral lipid greater than phosphatidylserine plus phosphatidylinositol greater than phosphatidylethanolamine. 30 min incubations with 32PO4(2-)-resulted in an isotope incorporation into phospholipids, phosphatidylcholine greater than phosphatidylserine plus phosphatidylinositol greater than phosphatidylethanolamine. After 'loading' with [3H]arachidonate and 32P, placing the strips in potassium-free media caused the following: there was an increased release of [3H]arachidonate from the tissue into the bathing solution. [3H]Arachidonate and 32P radioactivity in phosphatidylinositol fell without a change in phosphatidylinositol content. [3H]Arachidonate and 32P radioactivity in other phospholipid fractions was unchanged. Arachidonate specific activity fell and arachidonate content increased in the phosphatidylserine plus phosphatidylinositol fraction. [3]Arachidonate in neutral lipid did not change significantly. We conclude that exposure of taenia coli to potassium-free media activates turnover of phosphatidylinositol, which results in release of arachidonate.
我们研究了将豚鼠结肠带条浸入无钾培养基中对花生四烯酸储备及其他脂质组分的影响。用结肠带条在 Krebs 溶液中进行的对照研究表明,超过 97%的花生四烯酸以酯化形式存在于磷脂中,其分布如下:磷脂酰乙醇胺>磷脂酰胆碱>磷脂酰丝氨酸加磷脂酰肌醇。将结肠带条与与白蛋白结合的[3H]花生四烯酸一起孵育 30 分钟,导致该同位素掺入磷脂和中性脂质组分中,掺入量顺序为:磷脂酰胆碱>中性脂质>磷脂酰丝氨酸加磷脂酰肌醇>磷脂酰乙醇胺。用 32PO4(2-)孵育 30 分钟导致同位素掺入磷脂,掺入量顺序为:磷脂酰胆碱>磷脂酰丝氨酸加磷脂酰肌醇>磷脂酰乙醇胺。在用[3H]花生四烯酸和 32P“加载”后,将结肠带条置于无钾培养基中会导致以下情况:组织中[3H]花生四烯酸向浴液中的释放增加。磷脂酰肌醇中的[3H]花生四烯酸和 32P 放射性下降,而磷脂酰肌醇含量不变。其他磷脂组分中的[3H]花生四烯酸和 32P 放射性不变。磷脂酰丝氨酸加磷脂酰肌醇组分中的花生四烯酸比活性下降,花生四烯酸含量增加。中性脂质中的[3]花生四烯酸没有显著变化。我们得出结论,结肠带条暴露于无钾培养基会激活磷脂酰肌醇的周转,从而导致花生四烯酸的释放。