Suppr超能文献

猫血浆胆碱浓度的控制

The control of the plasma choline concentration in the cat.

作者信息

Gardiner J E, Paton W D

出版信息

J Physiol. 1972 Dec;227(1):71-86. doi: 10.1113/jphysiol.1972.sp010020.

Abstract
  1. Changes in choline concentration of the blood after injections or infusions of choline were studied in cats anaesthetized with chloralose.2. Single I.V. injections of choline 10-100 mumole/kg produced arterial plasma levels 1 min later corresponding to an apparent volume of initial distribution of 430 ml./kg. The concentration then declined rapidly (half-time, 1-2 min), with a later slower decline after large doses.3. Infusions of choline at a rate of 0.8 mumole/kg.min or greater produced steady rises in plasma level, corresponding to a clearance of 28.6 ml. plasma/kg.min. The half time of rate of approach to steady state was 7 min or less. Infusions at rates of 0.40 mumole/kg.min or less produced much smaller or negligible rises, suggesting mechanisms for disposal which were saturated at higher concentration. At low rates, little infused choline appeared in urine. At the end of an infusion, the plasma choline level usually fell without delay.4. Portal blood contained about 50% of the arterial level, renal venous blood 15-70%, caval blood 30-60%, and amniotic fluid 2.5%. Occlusion of renal coeliac or mesenteric arteries raised plasma choline, but relatively rapid choline removal still occurred in the eviscerate animal.5. After infusions of [methyl-(14)C]choline, the level of radioactivity retained in the circulation amounted to only a few per cent of the total dose infused. At low rates of infusion (0.0125-0.1 mumole/kg.min) the radioactivity represented only a small fraction of bio-assayable choline; but at 0.40 mumole/kg.min it came to exceed the concentration of free choline, indicating metabolic conversion. Only traces of (14)C were found in expired air, and only 1-1.5% of total infused radioactivity in the urine. After infusion of 150 mumole over 3 hr, high levels of radioactivity were found in liver, kidney, lung, brain and heart, but levels in muscle and spleen were comparable to that of blood.6. It was concluded that choline is rapidly lost from the blood, that the abdominal viscera, liver, kidney and lung are important extraction sites, that some partial metabolism occurs, the metabolites also being rapidly lost from blood, and that it is probable that choline lost to the tissues becomes bound in some form.
摘要
  1. 研究了用氯醛糖麻醉的猫在注射或输注胆碱后血液中胆碱浓度的变化。

  2. 静脉内单次注射10 - 100微摩尔/千克的胆碱,1分钟后动脉血浆水平对应的初始分布表观容积为430毫升/千克。随后浓度迅速下降(半衰期为1 - 2分钟),大剂量注射后后期下降较慢。

  3. 以0.8微摩尔/千克·分钟或更高的速率输注胆碱会使血浆水平持续升高,对应清除率为28.6毫升血浆/千克·分钟。达到稳态速率的半衰期为7分钟或更短。以0.40微摩尔/千克·分钟或更低的速率输注产生的升高要小得多或可忽略不计,这表明在较高浓度下饱和的处置机制。在低速率下,很少有输注的胆碱出现在尿液中。输注结束时,血浆胆碱水平通常会立即下降。

  4. 门静脉血中的胆碱含量约为动脉血水平的50%,肾静脉血为15 - 70%,腔静脉血为30 - 60%,羊水为2.5%。阻断肾动脉、腹腔动脉或肠系膜动脉会使血浆胆碱升高,但在去内脏动物中胆碱仍相对快速地被清除。

  5. 输注[甲基 - (14)C]胆碱后,循环中保留的放射性水平仅占输注总剂量的百分之几。在低输注速率(0.0125 - 0.1微摩尔/千克·分钟)下,放射性仅占生物可测定胆碱的一小部分;但在0.40微摩尔/千克·分钟时,它超过了游离胆碱的浓度,表明发生了代谢转化。在呼出气体中仅发现微量的(14)C,尿液中仅占总输注放射性的1 - 1.5%。在3小时内输注150微摩尔后,在肝脏、肾脏、肺、脑和心脏中发现了高水平的放射性,但肌肉和脾脏中的水平与血液中的相当。

  6. 得出的结论是,胆碱迅速从血液中消失,腹腔内脏、肝脏、肾脏和肺是重要的摄取部位,发生了一些部分代谢,代谢产物也迅速从血液中消失,并且输给组织的胆碱很可能以某种形式结合。

相似文献

1
The control of the plasma choline concentration in the cat.猫血浆胆碱浓度的控制
J Physiol. 1972 Dec;227(1):71-86. doi: 10.1113/jphysiol.1972.sp010020.
5
The kidney in regulation of plasma choline in the chicken.鸡体内肾脏对血浆胆碱的调节作用。
Am J Physiol. 1975 Feb;228(2):645-9. doi: 10.1152/ajplegacy.1975.228.2.645.

引用本文的文献

2
Uptake of free choline by isolated perfused rat liver.游离胆碱在离体灌注大鼠肝脏中的摄取。
Proc Natl Acad Sci U S A. 1980 Aug;77(8):4417-9. doi: 10.1073/pnas.77.8.4417.

本文引用的文献

1
2
The level of free choline in plasma.血浆中游离胆碱的水平。
J Physiol. 1952 Jun;117(2):234-40. doi: 10.1113/jphysiol.1952.sp004743.
3
Renal excretion of choline in the dog.
Am J Physiol. 1962 Feb;202:319-24. doi: 10.1152/ajplegacy.1962.202.2.319.
6
The mechanism of action of the hemicholiniums.半胆碱类药物的作用机制。
Int Rev Neurobiol. 1960;2:77-97. doi: 10.1016/s0074-7742(08)60120-8.
10
A p-terphenyl hemicholinium compound.一种对联三苯半胆碱化合物。
Br J Pharmacol. 1969 May;36(1):171P-172P. doi: 10.1111/j.1476-5381.1969.tb08314.x.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验