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脑单胺氧化酶(MAO)活性与蓝斑神经元放电频率之间的关系。

Relation between brain monoamine oxidase (MAO) activity and the firing rate of locus coeruleus neurons.

作者信息

Oreland L, Engberg G

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1986 Jul;333(3):235-9. doi: 10.1007/BF00512935.

DOI:10.1007/BF00512935
PMID:3762738
Abstract

Utilizing a specific "low substrate concentration technique", intrasynaptosomal MAO-A and MAO-B activities within the rat brain noradrenaline system were studied. It was found that mainly MAO-A was localized intrasynaptosomally, whereas MAO-B contributed with less than 15% of the total intrasynaptosomal MAO activity, a phenomenon that was also observed within the central dopamine system. It is suggested that the intrasynaptosomal pool of MAO in the noradrenaline and the dopamine systems may reflect the density of innervation of the respective system throughout the brain. In addition, the effects of various selective monoamine oxidase (MAO) inhibitors on the noradrenergic intrasynaptosomal MAO activity as well as on the neuronal firing rate of noradrenaline containing cells in the locus coeruleus (LC) were investigated. Pretreatment with the MAO-A selective inhibitors clorgyline (10 mg/kg, i.p., 1 h) or (+)-FLA 336 (1 mg/kg, i.p., 1 h) caused a significant depression (40%) of mean spontaneous firing rate of LC neurones, randomly encountered throughout the LC. The MAO-B selective inhibitor pargyline (10 mg/kg, i.p., 1 h) was found to lack effect in this regard. However, pretreatment with (-)-deprenyl (10 mg/kg, i.p., 1 h), equally a selective MAO-B inhibitor, markedly suppressed the spontaneous firing rate of LC units. This inhibition by (-)-deprenyl was blocked by pretreatment with SK&F 525 A (50 mg/kg, i.p., 30 min), an inhibitor of microsomal drug metabolizing enzymes. Thus, the depression of LC units by (-)-deprenyl seems to be executed by a metabolite, e.g. l-amphetamine.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

利用一种特定的“低底物浓度技术”,对大鼠脑去甲肾上腺素系统内突触小体内的单胺氧化酶A(MAO-A)和单胺氧化酶B(MAO-B)活性进行了研究。结果发现,主要是MAO-A定位于突触小体内,而MAO-B在突触小体总MAO活性中所占比例不到15%,这一现象在中枢多巴胺系统中也有观察到。提示去甲肾上腺素和多巴胺系统中突触小体内的MAO库可能反映了整个大脑中各系统的神经支配密度。此外,还研究了各种选择性单胺氧化酶(MAO)抑制剂对去甲肾上腺素能突触小体内MAO活性以及对蓝斑(LC)中含去甲肾上腺素细胞的神经元放电率的影响。用MAO-A选择性抑制剂氯吉兰(10毫克/千克,腹腔注射,1小时)或(+)-FLA 336(1毫克/千克,腹腔注射,1小时)预处理,可使在整个LC中随机遇到的LC神经元的平均自发放电率显著降低(40%)。发现MAO-B选择性抑制剂帕吉林(10毫克/千克,腹腔注射,1小时)在这方面没有作用。然而,用同样是选择性MAO-B抑制剂的(-)-司来吉兰(10毫克/千克,腹腔注射,1小时)预处理,可明显抑制LC单位的自发放电率。(-)-司来吉兰的这种抑制作用可被微粒体药物代谢酶抑制剂SK&F 525 A(50毫克/千克,腹腔注射,30分钟)预处理所阻断。因此,(-)-司来吉兰对LC单位的抑制作用似乎是由一种代谢产物,如l-苯丙胺执行的。(摘要截短于250字)

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本文引用的文献

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FURTHER STUDIES ON THE INHIBITION AND STIMULATION OF MICROSOMAL DRUG METABOLIZING ENZYMES OF RAT LIVER BY VARIOUS COMPOUNDS.多种化合物对大鼠肝脏微粒体药物代谢酶的抑制与刺激作用的进一步研究
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Norepinephrine-containing locus coeruleus neurons in behaving rats exhibit pronounced responses to non-noxious environmental stimuli.行为活跃的大鼠中含去甲肾上腺素的蓝斑神经元对非伤害性环境刺激表现出明显反应。
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Activity of norepinephrine-containing locus coeruleus neurons in behaving rats anticipates fluctuations in the sleep-waking cycle.行为大鼠中含去甲肾上腺素的蓝斑神经元的活动先于睡眠-觉醒周期的波动。
J Neurosci. 1981 Aug;1(8):876-86. doi: 10.1523/JNEUROSCI.01-08-00876.1981.
7
Monoamine oxidase type A: differences in selectivity towards l-norepinephrine compared to serotonin.A型单胺氧化酶:与5-羟色胺相比,对去甲肾上腺素选择性的差异。
Biochem Pharmacol. 1982 Dec 15;31(24):4061-6. doi: 10.1016/0006-2952(82)90656-6.
8
A new approach to the assessment of the potency of reversible monoamine oxidase inhibitors in vivo, and its application to (+)-amphetamine, p-methoxyamphetamine and harmaline.一种评估可逆性单胺氧化酶抑制剂体内效力的新方法及其在(+)-苯丙胺、对甲氧基苯丙胺和骆驼蓬碱中的应用。
Biochem Pharmacol. 1980 Oct 15;29(20):2781-9. doi: 10.1016/0006-2952(80)90012-x.
9
The monoamine oxidase inhibitors clorgyline and L-deprenyl also affect the uptake of dopamine, noradrenaline and serotonin by rat brain synaptosomal preparations.单胺氧化酶抑制剂氯吉兰和L-司来吉兰也会影响大鼠脑突触体制剂对多巴胺、去甲肾上腺素和5-羟色胺的摄取。
Biochem Pharmacol. 1980 Oct 15;29(20):2763-7. doi: 10.1016/0006-2952(80)90009-x.
10
Immunocytochemical demonstration of monoamine oxidase B in brain astrocytes and serotonergic neurons.脑星形胶质细胞和5-羟色胺能神经元中单胺氧化酶B的免疫细胞化学证明
Proc Natl Acad Sci U S A. 1982 Oct;79(20):6385-9. doi: 10.1073/pnas.79.20.6385.