Maines M D
Biochem J. 1980 Aug 15;190(2):315-21. doi: 10.1042/bj1900315.
The activity of 5-aminolaevulinate synthase, the rate-limiting enzyme of haem biosynthesis, is differentially distributed in various regions of the rat brain. The cerebellum possessed the highest enzyme activity of the eight regions studied. The cerebral cortex and the midbrain also exhibited high 5-aminolaevulinate synthase activity; the septum, hypothalamus, thalamus, amygdala and the hippocampus possessed much lower enzyme activity. However, the total porphyrin and haem contents of the different brain segments did not vary greatly. Mn(2+), when administered subcutaneously to rats, effectively inhibited the activity of 5-aminolaevulinate synthase in the cerebellum, midbrain and cerebral cortex; however, repeated injections of the metal ion neither decreased the haem and porphyrin contents of the brain nor induced haem oxygenase activity. Mn(2+) was not an effective inhibitor of 5-aminolaevulinate synthase activity in vitro. On the other hand, studies carried out with the liver in vivo suggested that Mn(2+) may alter the turnover rate of cellular haem and haemoproteins. In that event, it is likely that the inhibition of 5-aminolaevulinate synthase by Mn(2+) was in part a result of the inhibition of protein synthesis by the metal ion. It is postulated that the haem and porphyrin contents of the brain are maintained at a steady-state level, due in part to the refractoriness to inducers of the regulatory mechanism for haem catabolic enzymes and in part to the ability of the organ to utilize haem precursors derived from extraneuronal sources.
5-氨基酮戊酸合酶是血红素生物合成的限速酶,其活性在大鼠脑的不同区域呈差异分布。在所研究的八个区域中,小脑的酶活性最高。大脑皮层和中脑也表现出较高的5-氨基酮戊酸合酶活性;隔区、下丘脑、丘脑、杏仁核和海马体的酶活性则低得多。然而,不同脑段的总卟啉和血红素含量变化不大。当给大鼠皮下注射锰离子(Mn²⁺)时,它能有效抑制小脑、中脑和大脑皮层中5-氨基酮戊酸合酶的活性;然而,重复注射这种金属离子既没有降低脑中血红素和卟啉的含量,也没有诱导血红素加氧酶的活性。在体外,Mn²⁺不是5-氨基酮戊酸合酶活性的有效抑制剂。另一方面,在体内对肝脏进行的研究表明,Mn²⁺可能会改变细胞血红素和血红素蛋白的周转率。在这种情况下,Mn²⁺对5-氨基酮戊酸合酶的抑制作用可能部分是由于该金属离子对蛋白质合成的抑制。据推测,脑内血红素和卟啉的含量维持在稳态水平,部分原因是血红素分解代谢酶的调节机制对诱导剂不敏感,部分原因是该器官利用源自神经外来源的血红素前体的能力。