Daley J T, Brown M L, Watkins T, Traish A M, Huang Y H, Moreland R B, De Tejada I S
Department of Urology, Boston University School of Medicine, Massachusetts, USA.
J Urol. 1996 Apr;155(4):1482-7.
To investigate the effects of oxygen tension on prostanoid synthesis in rabbit penile corpus cavernosum tissue (RCC) in organ culture.
Strips of rabbit corpus cavernosum were incubated in organ culture media under varying oxygen conditions (0%, 12% and 21% oxygen), in the presence or absence of acetylcholine and arachidonate stimulation. Prostanoids were measured in collected media by radioimmunoassay. Prostaglandin H synthase (PGHS) protein levels and mRNA PGHS expression were measured under both 0% and 21% oxygen conditions.
Basal and acetylcholine-stimulated PGI2 release was progressively diminished as a function of diminishing oxygen tension (pO2 from approximately 165 to 25 mm.Hg). The basal and stimulated production of other prostanoids, thromboxane A2, PGF2alpha, and PGE2, was also significantly inhibited under 0% oxygen (approximately 25 mm.Hg) conditions. However, incubation under 0% oxygen did not alter PGHS protein levels nor mRNA PGHS expression. Cavernosal strips incubated under 0% oxygen but supplemented with exogenous arachidonate (10 microM.) maintained significantly lower PGI2 production than tissues exposed to 21% oxygen (approximately 165 mm.Hg).
These data demonstrate that oxygen tension regulates prostaglandin production in corporal tissue. The reduction in prostanoid production during hypoxia can be attributed to inhibition of PGHS activity rather than the expression of the enzyme. In view of the role of PGI2 as an inhibitor of platelet aggregation and white cell-endothelial adhesion, our findings may provide mechanistic insight into the alteration in corporal blood homeostasis ischemic-hypoxic priapism.
研究氧张力对器官培养的兔阴茎海绵体组织(RCC)中前列腺素合成的影响。
将兔海绵体条带在不同氧条件(0%、12%和21%氧)下于器官培养基中孵育,同时存在或不存在乙酰胆碱和花生四烯酸刺激。通过放射免疫测定法测量收集培养基中的前列腺素。在0%和21%氧条件下测量前列腺素H合酶(PGHS)蛋白水平和mRNA PGHS表达。
随着氧张力降低(pO2从约165降至25 mmHg),基础和乙酰胆碱刺激的前列环素I2(PGI2)释放逐渐减少。在0%氧(约25 mmHg)条件下,其他前列腺素血栓素A2、前列腺素F2α和前列腺素E2的基础和刺激产生也受到显著抑制。然而,在0%氧条件下孵育并未改变PGHS蛋白水平或mRNA PGHS表达。在0%氧条件下孵育但补充外源性花生四烯酸(10 μM)的海绵体条带,其PGI2产生显著低于暴露于21%氧(约165 mmHg)的组织。
这些数据表明氧张力调节海绵体组织中的前列腺素产生。缺氧期间前列腺素产生的减少可归因于PGHS活性的抑制而非该酶的表达。鉴于PGI2作为血小板聚集和白细胞-内皮细胞黏附抑制剂的作用,我们的发现可能为缺血-缺氧性阴茎异常勃起时海绵体血液稳态改变提供机制性见解。