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兔子宫内膜对3H-(-)-去甲肾上腺素的可卡因敏感性积累及O-甲基化特性

Characteristics of the cocaine-sensitive accumulation and O-methylation of 3H-(-)-noradrenaline by rabbit endometrium.

作者信息

Kennedy J A, de la Lande I S

机构信息

Department of Clinical and Experimental Pharmacology, University of Adelaide, South Australia.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1987 Aug;336(2):148-54. doi: 10.1007/BF00165798.

Abstract
  1. The extraneuronal uptake and O-methylation of 2,5,6 3H-(-)-noradrenaline was studied in segments of uterine endometrium from rabbits pretreated with 17 beta-oestradiol and progesterone. 2. The uptake of 3H-noradrenaline was measured in MAO- and COMT-inhibited tissues and obeyed Michaelis-Menten kinetics with an apparent Km of 78 mumol/l and a Vmax of 5.4 nmol/g min. Uptake was inhibited by low Na+, and by potential substrates in the order dopamine greater than (-)adrenaline greater than (-)isoprenaline = 5-hydroxytryptamine. 3. Following uptake at 1.2 mumol/l, efflux of 3H-noradrenaline was slow and appeared to be from two compartments, of which the first (I) had a t1/2 of 53 min and a capacity of 1.8 nmol/g. The presence of the second compartment (II) was inferred from the tissue content of 3H after 60 min of efflux, which was 3-4 times greater than predicted if the 3H was present in compartment I only. Following incubation with 3H-noradrenaline in the presence of cocaine 30 mumol/l the 3H efflux was rapid and the combined capacities of compartments I and II were greatly decreased. 4. 3H-NMN formation, measured in MAO-inhibited tissues, obeyed Michaelis-Menten kinetics with a half-saturating outside concentration of 12 mumol/l and a Vmax of 0.9 nmol/g X min. The formation was inhibited by the neuronal uptake inhibitors, desipramine 3 mumol/l and metaraminol 100 mumol/l (each by 80%), but was unaffected by the extraneuronal uptake inhibitor, NMN 100 mumol/l, and by oxytetracycline 100 mumol/l and methoxamine 10 mumol/l. 5.(ABSTRACT TRUNCATED AT 250 WORDS)
摘要
  1. 研究了用17β-雌二醇和孕酮预处理的兔子宫内膜片段中2,5,6 3H-(-)-去甲肾上腺素的神经元外摄取和O-甲基化。2. 在单胺氧化酶(MAO)和儿茶酚-O-甲基转移酶(COMT)抑制的组织中测量3H-去甲肾上腺素的摄取,其遵循米氏动力学,表观Km为78μmol/L,Vmax为5.4nmol/g·min。低钠和潜在底物(多巴胺>(-)肾上腺素>(-)异丙肾上腺素 = 5-羟色胺)可抑制摄取。3. 在1.2μmol/L摄取后,3H-去甲肾上腺素的流出缓慢,似乎来自两个区室,其中第一个区室(I)的半衰期为53分钟,容量为1.8nmol/g。第二个区室(II)的存在是根据流出60分钟后组织中3H的含量推断出来的,如果3H仅存在于区室I中,该含量比预测值高3 - 4倍。在30μmol/L可卡因存在下与3H-去甲肾上腺素孵育后,3H流出迅速,区室I和II的总容量大大降低。4. 在MAO抑制的组织中测量的3H-NMN形成遵循米氏动力学,半饱和外界浓度为12μmol/L,Vmax为0.9nmol/g·min。该形成受到神经元摄取抑制剂3μmol/L地昔帕明和100μmol/L间羟胺(各抑制80%)的抑制,但不受神经元外摄取抑制剂100μmol/L NMN、100μmol/L土霉素和10μmol/L甲氧明的影响。5.(摘要截断于250字)

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