Vanhatalo S, Soinila S
Department of Anatomy, Institute of Biomedicine, University of Helsinki, Finland.
Exp Neurol. 1999 Jun;157(2):305-16. doi: 10.1006/exnr.1999.7053.
In the present study we have further studied the previous findings that rat hypothalamic dopaminergic neuronal cell groups may express tryptophan hydroxylase (TpH), the serotonin synthesizing enzyme, without a detectable serotonin synthesis. Chemical and mechanical neuronal injuries, namely colchicine treatment and axonal transection, respectively, were performed, and distributions of neurons exhibiting immunoreactivity for TpH and/or tyrosine hydroxylase (TH), the dopamine synthesizing enzyme, were analyzed throughout the hypothalamic periventricular and arcuate nuclei. After colchicine treatment there was a statistically significant 87% (P = 0,01) increase in the number of TpH expressing neurons, while TH expression remained essentially similar. Axonal transection resulted also in a statistically significant 131% (P < 0,01) increase in the number of TpH expressing neurons, while TH expression was not significantly altered. All TpH expression coexisted with TH expression, and the induction of TpH expression by neuronal injuries occurred evenly throughout the rostrocaudal length of the territory studied. A possible serotonin synthesis by TpH was examined by giving drugs that increase brain serotonin synthesis, but no immunohistochemically detectable serotonin synthesis could be found in any of the TpH expressing neurons. Finally the possibility was studied that the relative shortage of the cofactor tetrahydrobiopterin would limit serotonin synthesis. However, an administration of tetrahydrobiopterin did not result in detectable serotonin synthesis in these neurons. Taken together these results suggest that dopaminergic neurons in the hypothalamic periventricular and arcuate nuclei are able to express TpH, this expression is induced after neuronal injury, and this induction occurs similarly throughout the territories studied. TpH expression occurs independently of TH expression, and the newly expressed TpH appears not to synthesize serotonin, regardless of pharmacological pretreatments. Thus, our findings (i) support the idea that neurons may possess inducible expression of nonfunctional transmitter-synthesizing enzymes, in this case TpH, and (ii) suggest that expression of an enzyme synthesizing a certain transmitter may not necessarily imply the corresponding transmitter phenotype.
在本研究中,我们进一步研究了先前的发现,即大鼠下丘脑多巴胺能神经元细胞群可能表达色氨酸羟化酶(TpH),即5-羟色胺合成酶,但未检测到5-羟色胺的合成。分别进行了化学性和机械性神经元损伤,即秋水仙碱处理和轴突横断,并分析了整个下丘脑室周核和弓状核中对TpH和/或酪氨酸羟化酶(TH,多巴胺合成酶)呈免疫反应性的神经元分布。秋水仙碱处理后,表达TpH的神经元数量有统计学意义地增加了87%(P = 0.01),而TH表达基本保持相似。轴突横断也导致表达TpH的神经元数量有统计学意义地增加了131%(P < 0.01),而TH表达没有显著改变。所有TpH表达都与TH表达共存,并且神经元损伤诱导的TpH表达在所研究区域的整个头尾长度上均匀发生。通过给予增加脑内5-羟色胺合成的药物来检测TpH是否可能合成5-羟色胺,但在任何表达TpH的神经元中均未发现免疫组化可检测到的5-羟色胺合成。最后研究了辅因子四氢生物蝶呤相对缺乏会限制5-羟色胺合成的可能性。然而,给予四氢生物蝶呤并未导致这些神经元中可检测到的5-羟色胺合成。综合这些结果表明,下丘脑室周核和弓状核中的多巴胺能神经元能够表达TpH,这种表达在神经元损伤后被诱导,并且这种诱导在所研究的区域中类似地发生。TpH表达独立于TH表达发生,并且新表达的TpH似乎不合成5-羟色胺,无论药理学预处理如何。因此,我们的发现(i)支持神经元可能具有非功能性递质合成酶的可诱导表达这一观点,在这种情况下为TpH,并且(ii)表明合成某种递质的酶的表达不一定意味着相应的递质表型。