Kawata R, Urade Y, Tachibana M, Mizukoshi O
Department of Otolaryngology, Kyoto Prefectual University of Medicine, Japan.
Prostaglandins. 1988 Feb;35(2):173-84. doi: 10.1016/0090-6980(88)90085-8.
The exogenous and endogenous syntheses of prostaglandins (PG's) by the cochlea of adult mongolian gerbils were studied in vitro. After incubation of the whole membraneous cochlea with [3H]-arachidonic acid (AA), syntheses of PGF2 alpha, 6-keto PGF1 alpha, PGE2, thromboxane (TX) P2 and PGD2 were evidenced in this order. The synthesis of radioactive PG's was almost completely inhibited by incubation with 10(-5) M indomethacin. No significant amounts of those PG's were detected by radioimmunoassay (RIA) in the cochlea obtained from animals killed by microwave irradiation at 5.0 kw for 0.8 sec. However, when the homogenate of the whole membraneous cochlea obtained from animals without microwave irradiation was incubated at 37 degrees C for 0-15 min, PGD2, PGE2, PGF2 alpha and 6-keto PGF1 alpha were found to be formed from endogenous AA in the cochlea by RIA. PG's were formed already at 0 time to considerable level (PGD2, PGF2 alpha and 6-keto PGF1 alpha, 90-120 pg/cochlea; PGE2, 370 pg/cochlea), reached to the maximum level (PGD2, PGF2 alpha and 6-keto PGF1 alpha, 170-200 pg/cochlea; PGE2, 500 pg/cochlea) at a 5-min incubation, and then gradually decreased. On the other hand, the amount of TXB2 was lower than the detection limit by RIA (less than 50 pg/cochlea) even after the incubation. The cochlea was dissected into three parts: organ of Corti + modiolus (OC + M), lateral wall (LW), and cochlear nerve (CN), and then PG's formed by these tissues were determined after a 5-min incubation of the homogenates. In the CN and OC + M, PGE2 was the major PG (100 and 160 pg/tissue, respectively), and the amounts of PGD2, PGF2 alpha and 6-keto PGF1 alpha were about 1/3 of those of PGE2. In the LW, the amounts of PGD2, PGE2, PGF2 alpha and 6-keto PGF1 alpha were about the same level (70-100 pg/LW).
对成年蒙古沙鼠耳蜗中前列腺素(PGs)的外源性和内源性合成进行了体外研究。将整个膜性耳蜗与[3H] - 花生四烯酸(AA)孵育后,依次检测到PGF2α、6 - 酮基PGF1α、PGE2、血栓素(TX)P2和PGD2的合成。用10(-5)M吲哚美辛孵育几乎完全抑制了放射性PGs的合成。在通过5.0千瓦微波照射0.8秒处死的动物的耳蜗中,放射免疫分析(RIA)未检测到大量的这些PGs。然而,当将未经过微波照射的动物的整个膜性耳蜗匀浆在37℃孵育0 - 15分钟时,通过RIA发现耳蜗中的内源性AA可形成PGD2、PGE2、PGF2α和6 - 酮基PGF1α。PGs在0时刻就已形成至相当水平(PGD2、PGF2α和6 - 酮基PGF1α,90 - 120 pg/耳蜗;PGE2,370 pg/耳蜗),在孵育5分钟时达到最高水平(PGD2、PGF2α和6 - 酮基PGF1α,170 - 200 pg/耳蜗;PGE2, 500 pg/耳蜗),然后逐渐下降。另一方面,即使孵育后,TXB2的量也低于RIA的检测限(小于50 pg/耳蜗)。将耳蜗分为三部分:柯蒂氏器 + 蜗轴(OC + M)、外侧壁(LW)和耳蜗神经(CN),然后在匀浆孵育5分钟后测定这些组织形成的PGs。在CN和OC + M中,PGE2是主要的PG(分别为100和160 pg/组织),PGD2、PGF2α和6 - 酮基PGF1α的量约为PGE2的1/3。在LW中,PGD2、PGE2、PGF2α和6 - 酮基PGF1α的量大致相同(70 - 100 pg/LW)。