De Matteis F, Ray D E
J Neurochem. 1982 Aug;39(2):551-6. doi: 10.1111/j.1471-4159.1982.tb03980.x.
Rats were injected intraventricularly with 5-amino[4-14C]laevulinate and the radioactivity recovered in the total cerebellum homogenate and in its haem and porphyrin fractions was determined in time. Two phases could be distinguished in the decline of haem radioactivity, suggesting labelling of at least two pools of widely different turnover rates. Succinyl acetone, when injected intraventricularly, caused a marked and long-lasting inhibition of cerebellar 5-aminolaevulinate dehydratase activity and a corresponding inhibition of the incorporation of [14C]5-aminolaevulinate into cerebellar haem in vivo. Inhibition of cerebellar haem biosynthesis by succinylacetone was followed by stimulation of the first enzyme of the pathway, 5-aminolaevulinate synthase, whereas intraventricular injection of haematin led to a significant depression of the activity of the enzyme. This suggested that the cerebellar 5-aminolaevulinate synthetase is regulated by haem through a negative feedback mechanism. Rats given repeated doses of succinylacetone, so as to maintain 80% inhibition of their cerebellar 5-aminolaevulinate dehydratase activity for 5 days, failed to exhibit any obvious symptoms of toxicity but became more sensitive to the neurotoxic effects of large intraventricular doses of 5-aminolaevulinate.
向大鼠脑室内注射5-氨基[4-¹⁴C] - 酮戊酸,并及时测定全小脑匀浆及其血红素和卟啉组分中回收的放射性。血红素放射性下降可分为两个阶段,这表明至少标记了两个周转率差异很大的池。脑室内注射琥珀酰丙酮会导致小脑5-氨基酮戊酸脱水酶活性受到显著且持久的抑制,并相应抑制[¹⁴C] - 5-氨基酮戊酸在体内掺入小脑血红素。琥珀酰丙酮抑制小脑血红素生物合成后,该途径的第一个酶5-氨基酮戊酸合酶会受到刺激,而脑室内注射血红素会导致该酶活性显著降低。这表明小脑5-氨基酮戊酸合酶受血红素通过负反馈机制调节。给大鼠反复注射琥珀酰丙酮,使其小脑5-氨基酮戊酸脱水酶活性持续5天受到80%的抑制,大鼠未表现出任何明显的毒性症状,但对大剂量脑室内注射5-氨基酮戊酸的神经毒性作用变得更加敏感。