Schaub R G, Meyers K M
Res Commun Chem Pathol Pharmacol. 1975 Jan;10(1):29-36.
"Scottie Cramp" is a genetic neurologic disease which occurs in the Scottish terrier breed of dogs. Decreasing central nervous system (CNS) concentrations of serotonin (5-HT) via para-chlorophenylalanine (pCPA) will profoundly increase the severity of the disease although the basic defect does not involve serotonergic neurons. The purpose of this study was to attempt to correlate the effect of p-CPA on the clinical signs of the disease with the alteration in serotonin synthesis and concentration in the CNS. Synthesis was estimated by following the rise in cisternal cerebrospinal fluid (CSF) 5-hydroxyindoleacetic acid (5-HIAA) concentrations with time following probenecid injection. Concentration of serotonin in the CNS was estimated by measuring cisternal CSF 5-HIAA concentrations. The results suggest that serotonin may be synthesized in excess of neuronal transmitter needs and that the estimation of whole brain turnover rates and concentrations of 5-HT may not yield a true measure of serotonergic neuronal activity.
“斯科特痉挛症”是一种发生在苏格兰梗犬品种中的遗传性神经疾病。通过对氯苯丙氨酸(pCPA)降低中枢神经系统(CNS)中血清素(5-HT)的浓度,会显著增加该疾病的严重程度,尽管其基本缺陷并不涉及血清素能神经元。本研究的目的是试图将p-CPA对该疾病临床症状的影响与中枢神经系统中血清素合成及浓度的改变联系起来。通过在注射丙磺舒后,随时间追踪脑池脑脊液(CSF)中5-羟吲哚乙酸(5-HIAA)浓度的升高来估算合成情况。通过测量脑池脑脊液中5-HIAA的浓度来估算中枢神经系统中血清素的浓度。结果表明,血清素的合成可能超过神经元递质的需求,并且对全脑周转率和5-HT浓度的估算可能无法真正衡量血清素能神经元的活性。