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本文引用的文献

1
The oxygen consumption and carbohydrate metabolism of the retractor muscle of the foot of Mytilus edulis.紫贻贝足部牵缩肌的耗氧量与碳水化合物代谢
J Physiol. 1936 Jun 10;87(1):56-66. doi: 10.1113/jphysiol.1936.sp003388.
2
Electrolyte and water metabolism of rabbit kidney slices; effect of metabolic inhibitors.兔肾切片的电解质和水代谢;代谢抑制剂的作用。
Am J Physiol. 1951 Oct;167(1):206-23. doi: 10.1152/ajplegacy.1951.167.1.206.
3
Studies on potassium accumulation by rabbit kidney slices; effect of metabolic activity.家兔肾切片钾蓄积的研究;代谢活性的影响。
Am J Physiol. 1951 Apr 1;165(1):113-27. doi: 10.1152/ajplegacy.1951.165.1.113.
4
Osmoregulation in surviving slices from the kidneys of adult rats.成年大鼠肾脏存活切片中的渗透调节
Proc R Soc Lond B Biol Sci. 1950 Oct 13;137(888):378-402. doi: 10.1098/rspb.1950.0048.
5
Changes in the water and electrolyte content of rat-liver slices in vitro.大鼠肝脏切片体外水和电解质含量的变化
Biochim Biophys Acta. 1959 Nov;36:203-13. doi: 10.1016/0006-3002(59)90085-x.
6
SELECTIVE ACCUMULATION OF POTASSIUM ION BY GEL AND KIDNEY SLICES.凝胶和肾切片对钾离子的选择性积累
Biochim Biophys Acta. 1964 Nov 29;88:593-605. doi: 10.1016/0926-6577(64)90102-0.
7
Maintenance of concentration gradients and regulation of cell volume.维持浓度梯度和调节细胞体积。
Ann N Y Acad Sci. 1959 Feb 6;72(12):396-404. doi: 10.1111/j.1749-6632.1959.tb44168.x.
8
On the mechanism of fluid exchange of tissues in vitro.关于体外组织液交换的机制
Biochem J. 1956 Feb;62(2):241-8. doi: 10.1042/bj0620241.
9
[Electrolyte accumulation and osmoregulation in tissue slices].[组织切片中的电解质蓄积与渗透调节]
Helv Physiol Pharmacol Acta. 1953;11(1):96-121.
10
A kinetic study of the state of potassium in kidney tissue.肾脏组织中钾状态的动力学研究。
Biochim Biophys Acta. 1965 Nov 29;109(2):454-66. doi: 10.1016/0926-6585(65)90171-8.

高浓度电解质对非代谢组织切片肿胀的影响。

The effects of high concentrations of an electrolyte on the swelling of non-metabolizing tissue slices.

作者信息

Davey K J, Skegg D C

出版信息

J Physiol. 1971 Feb;212(3):641-53. doi: 10.1113/jphysiol.1971.sp009347.

DOI:10.1113/jphysiol.1971.sp009347
PMID:5557065
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1395728/
Abstract
  1. Rat kidney cortical slices, with metabolism suppressed by iodoacetate, were incubated anaerobically at 26 degrees C in hyperosmotic saline media. Changes in tissue composition with time, up to 12 hr, were studied. Despite initial shrinkage, gross swelling occurred, even in saline media of more than twice the concentration of normal extracellular fluid.2. The composition of non-metabolizing kidney slices incubated at 26 degrees C in a balanced saline medium containing 7 g polyethylene glycol 6000 (PEG 6000)/100 ml. was determined at intervals up to 12 hr. The tissue water, sodium and chloride contents had reached constant levels by 6 hr. Potassium continued to leak slowly from the tissue, but there was no significant further loss between 10 and 12 hr.3. Non-metabolizing kidney slices were incubated in PEG medium containing additional quantities of either a non-electrolyte (400 m-osmole glucose/kg H(2)O) or an electrolyte (400 m-osmole NaCl/kg H(2)O), both of which penetrated the tissue to attain approximately uniform concentrations in cells and media. Whereas the slices in the glucose medium attained the same equilibrium water content as those incubated in PEG medium alone, the final water content of slices in the medium containing additional NaCl was significantly lower. This difference might have resulted from depression of intracellular colloid osmotic pressure by the high salt concentration.
摘要
  1. 用碘乙酸抑制代谢的大鼠肾皮质切片,于26℃在高渗盐溶液培养基中进行厌氧孵育。研究了长达12小时内组织成分随时间的变化。尽管最初有收缩,但即使在浓度超过正常细胞外液两倍的盐溶液中,仍出现了明显的肿胀。

  2. 在含有7g聚乙二醇6000(PEG 6000)/100ml的平衡盐溶液培养基中于26℃孵育不进行代谢的肾切片,每隔一定时间直至12小时测定其成分。到6小时时,组织水、钠和氯含量已达到恒定水平。钾继续从组织中缓慢渗漏,但在10至12小时之间没有明显的进一步损失。

  3. 将不进行代谢的肾切片在含有额外数量的非电解质(400毫渗摩尔葡萄糖/千克H₂O)或电解质(400毫渗摩尔氯化钠/千克H₂O)的PEG培养基中孵育,这两种物质都能穿透组织,使细胞和培养基中的浓度大致均匀。在葡萄糖培养基中的切片达到了与仅在PEG培养基中孵育的切片相同的平衡含水量,而在含有额外氯化钠的培养基中的切片最终含水量显著更低。这种差异可能是由于高盐浓度降低了细胞内胶体渗透压所致。