Horrobin D F, Manku M S
Med Hypotheses. 1977 Mar-Apr;3(2):71-86. doi: 10.1016/0306-9877(77)90057-3.
We have recently found that local anaesthetic, anti-malarial, anti-arrhythmic, tricyclic antidepressant and methyl xanthine compounds behave as prostaglandin antagonists at drug concentrations readily attainable in human body fluids. We have also found that various hormones, including prolactin, vasopressin and angiotensin when present in physiological concentrations can be potent stimulators of prostaglandin synthesis. Cortisol has no effect on basal prostaglandin systhesis but in physiological concentrations is able to reverse the effects of other hormones. The drugs are thought to act mainly by interfering with either calcium interactions with membranes, or with cyclic nucleotide synthesis or degradation or with nucleic acid function. We propose that prostaglandins play crucial roles at all three points. The hypothesis leads to new approaches to many aspects of cell regulation, to the functions of many systems, especially the neuromuscular, cardiovascular, renal and respiratory systems. It also has profound implications for drug design and evaluation and for the understanding of many clinical disorders.
我们最近发现,局部麻醉药、抗疟疾药、抗心律失常药、三环类抗抑郁药和甲基黄嘌呤化合物在人体体液中易于达到的药物浓度下表现为前列腺素拮抗剂。我们还发现,各种激素,包括催乳素、血管加压素和血管紧张素,当以生理浓度存在时,可成为前列腺素合成的有效刺激物。皮质醇对基础前列腺素合成没有影响,但在生理浓度下能够逆转其他激素的作用。这些药物被认为主要通过干扰钙与膜的相互作用、环核苷酸的合成或降解或核酸功能来发挥作用。我们提出,前列腺素在所有这三个方面都起着关键作用。这一假说为细胞调节的许多方面、许多系统的功能,特别是神经肌肉、心血管、肾脏和呼吸系统的功能,带来了新的研究方法。它对药物设计和评估以及对许多临床疾病的理解也具有深远意义。