Sakato M
Nihon Yakurigaku Zasshi. 1975 Jul;71(5):445-55.
Prostaglandin (PG) E1, PGE2 and PGF2alpha and their biosynthesis inhibitor, indomethacin, were tested for their effects on the inhibitory responses of taenia induced by electrical stimulation of adrenergic and/or non-adrenergic inhibitory nerves in the perivascular nerve-taenia preparation isolated from guinea-pig caecum. The response to adrenergic nerve stimulation was considerably reduced by PGE1 and PGE2, while it was little affected by PGF2alpha. Although PGE1 and PGE2 produced contraction of taenia, it may be possible to dismiss from consideration their action of contraction of taenia in accounting for their inhibitory effect on the response to nerve stimulation since the following observations were made, 1) when the taenia were contracted by histamine, the response to adrenergic nerve stimulation was not reduced and 2) in the presence of polyphloretin phosphate, PGE1 and PGE2 did not contract taenia but reduced the response to adrenergic nerve stimulation. In the presence of indomethacin, the response to adrenergic nerve stimulation was increased greatly. On the contrary, the inhibitory response to non-adrenergic inhibitory nerve stimulation was not affected by application of PGE1, PGE2, PGF2alpha and indomethacin. These results suggest that endogenous PG of E series in guinea-pig taenia may play a role in modulating adrenergic neurotransmission. Attempts to demonstrate that PG could operate on a non-adrenergic inhibitory neurotransmission by a negative feedback mechanism were without success.
前列腺素(PG)E1、PGE2和PGF2α及其生物合成抑制剂吲哚美辛,在从豚鼠盲肠分离的血管周围神经-绦虫制备物中,被测试了它们对电刺激肾上腺素能和/或非肾上腺素能抑制神经所诱导的绦虫抑制反应的影响。PGE1和PGE2可显著降低对肾上腺素能神经刺激的反应,而PGF2α对此影响很小。尽管PGE1和PGE2可使绦虫收缩,但鉴于以下观察结果,在解释它们对神经刺激反应的抑制作用时,可排除其使绦虫收缩的作用:1)当绦虫因组胺而收缩时,对肾上腺素能神经刺激的反应并未降低;2)在聚磷酸根皮苷存在的情况下,PGE1和PGE2并未使绦虫收缩,但降低了对肾上腺素能神经刺激的反应。在吲哚美辛存在的情况下,对肾上腺素能神经刺激的反应大幅增加。相反,对非肾上腺素能抑制神经刺激的抑制反应不受PGE1、PGE2、PGF2α和吲哚美辛应用的影响。这些结果表明,豚鼠绦虫中内源性E系列PG可能在调节肾上腺素能神经传递中起作用。试图证明PG可通过负反馈机制作用于非肾上腺素能抑制性神经传递,但未成功。