Marazziti D, Pietrini P, Martini C, Giannaccini G, Perugi G, Placidi G F, Cassano G B, Lucacchini A
Institute of Psychiatric Clinic, University of Pisa, Italy.
Neuropsychobiology. 1987;18(2):74-6. doi: 10.1159/000118396.
We investigated the possible existence of endogenous compounds acting on benzodiazepine central receptors in the serum of patients with panic attacks or depression. Our results show the presence of a substance which inhibits the 3H-flunitrazepam binding specifically in the samples taken from the patients' groups, and which is not present in normal controls, in the range of concentrations used. This compound has a molecular weight below 1,000 daltons, is heat-stable, and resistant to proteolytic degradation. The demonstration of this inhibitor opens new perspectives in the study of the biochemistry of anxiety.
我们研究了恐慌症或抑郁症患者血清中作用于苯二氮䓬中枢受体的内源性化合物的可能存在情况。我们的结果表明,在取自患者组的样本中存在一种物质,它能特异性抑制3H-氟硝西泮结合,而在正常对照组中,在所使用的浓度范围内不存在这种物质。这种化合物的分子量低于1000道尔顿,具有热稳定性,且对蛋白水解降解具有抗性。这种抑制剂的发现为焦虑症生物化学研究开辟了新的前景。