Mathiau P, Reynier-Rebuffel A M, Issertial O, Callebert J, Decreme C, Aubineau P
Laboratoire de Recherches Cérébrovasculaires, CNRS U.A.641, Paris, France.
Neuroscience. 1993 Feb;52(3):657-65. doi: 10.1016/0306-4522(93)90414-b.
Neurochemical studies performed in vivo have suggested that serotonin-containing and -synthesizing nerves, originating in the raphe nuclei, directly innervate pial blood vessels. Nerve fibres of these vessels have been shown by immunocytochemistry to contain tryptophan hydroxylase (the rate-limiting enzyme of serotonin synthesis) but no serotonin. The present study examines this contradiction by measuring in vitro the tryptophan hydroxylase activity of rat cerebral vessels and femoral arteries (which also contain tryptophan hydroxylase-immunopositive nerves), and comparing them to the tryptophan hydroxylase activity of the rat pineal body, raphe nuclei and brain cortex under identical conditions. Oxygenated incubation solutions contained either [14C]- or "cold" L-tryptophan (2 x 10(-5) to 5 x 10(-4) M) and NSD-1015 (3-hydroxybenzylhydrazine) which inhibits the decarboxylation of 5-hydroxytryptophan, the second step of serotonin synthesis. Tissue fragments were incubated for 35-60 min. High-performance liquid chromatography (on tissue extracts and incubation solutions) as well as determination of 14C activity in the 5-hydroxytryptophan fraction of elution from tissue extracts showed that the pineal body, the raphe nuclei and cortical slices synthesize various amounts of 5-hydroxytryptophan under our experimental conditions. All these tissues contained serotonin. Femoral arteries, but not cerebral vessels, also contained small amounts of serotonin stored before incubation, probably in mast cells. In contrast to brain tissues, no measurable amounts of "cold" or [14C]5-hydroxytryptophan were found in cerebral blood vessel and femoral artery extracts or incubation solutions. Under identical experimental conditions, sympathetic nerves of both types of vessels were able to synthesize large amounts of L-DOPA when incubation solutions contained L-tyrosine instead of L-tryptophan.(ABSTRACT TRUNCATED AT 250 WORDS)
体内进行的神经化学研究表明,起源于中缝核的含5-羟色胺及合成5-羟色胺的神经直接支配软脑膜血管。免疫细胞化学显示,这些血管的神经纤维含有色氨酸羟化酶(5-羟色胺合成的限速酶),但不含5-羟色胺。本研究通过在体外测量大鼠脑血管和股动脉(其中也含有色氨酸羟化酶免疫阳性神经)的色氨酸羟化酶活性,并在相同条件下将其与大鼠松果体、中缝核和大脑皮质的色氨酸羟化酶活性进行比较,来研究这一矛盾之处。充氧的孵育溶液含有[14C]-或“冷”L-色氨酸(2×10⁻⁵至5×10⁻⁴M)以及NSD-1015(3-羟基苄基肼),后者可抑制5-羟色氨酸脱羧,即5-羟色胺合成的第二步。将组织碎片孵育35至60分钟。高效液相色谱法(对组织提取物和孵育溶液进行分析)以及对组织提取物洗脱液中5-羟色氨酸部分的14C活性测定表明,在我们的实验条件下,松果体、中缝核和皮质切片合成了不同量的5-羟色氨酸。所有这些组织都含有5-羟色胺。股动脉而非脑血管在孵育前也含有少量储存的5-羟色胺,可能存在于肥大细胞中。与脑组织不同,在脑血管和股动脉提取物或孵育溶液中未发现可测量量的“冷”或[14C]5-羟色氨酸。在相同实验条件下,当孵育溶液含有L-酪氨酸而非L-色氨酸时,两种血管的交感神经都能够合成大量L-多巴。(摘要截取自250词)