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本文引用的文献

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ELECTROCHEMICAL CHANGES ASSOCIATED WITH THE FORMATION OF THE AQUEOUS HUMOUR.与房水形成相关的电化学变化
Br J Ophthalmol. 1961 Mar;45(3):202-17. doi: 10.1136/bjo.45.3.202.
2
Some considerations on the salt content of fresh and old ox corneae.关于新鲜和陈旧牛角膜盐含量的一些考量
Br J Ophthalmol. 1949 Mar;33(3):175-82. doi: 10.1136/bjo.33.3.175.
3
Osmotic behaviour of the epithelial cells of frog skin.蛙皮上皮细胞的渗透行为。
Acta Physiol Scand. 1961 Nov-Dec;53:348-65. doi: 10.1111/j.1748-1716.1961.tb02293.x.
4
The hydration of the cornea.角膜的水合作用。
Biochem J. 1955 Jan;59(1):24-8. doi: 10.1042/bj0590024.
5
ELECTRICAL POTENTIALS OF CHOROID PLEXUS OF THE RABBIT.兔脉络丛的电位
J Neurosurg. 1965 Apr;22:344-51. doi: 10.3171/jns.1965.22.4.0344.
6
THE MECHANISM OF BICARBONATE REABSORPTION IN THE PROXIMAL AND DISTAL TUBULES OF THE KIDNEY.肾脏近端小管和远端小管中碳酸氢根重吸收的机制
J Clin Invest. 1965 Feb;44(2):278-90. doi: 10.1172/JCI105142.
7
COUPLED TRANSPORT OF SOLUTE AND WATER ACROSS RABBIT GALLBLADDER EPITHELIUM.溶质和水通过兔胆囊上皮的耦合转运
J Clin Invest. 1964 Dec;43(12):2249-65. doi: 10.1172/JCI105099.
8
TRANSPORT OF SALT AND WATER IN RABBIT AND GUINEA PIG GALL BLADDER.兔和豚鼠胆囊中盐与水的转运
J Gen Physiol. 1964 Sep;48(1):1-14. doi: 10.1085/jgp.48.1.1.
9
DIRECT OBSERVATION OF SECRETORY PUMPING IN VITRO OF THE RABBIT EYE CILIARY PROCESSES. INFLUENCE OF ION MILIEU AND CARBONIC ANHYDRASE INHIBITION.兔眼睫状体体外分泌泵作用的直接观察。离子环境及碳酸酐酶抑制作用的影响。
Invest Ophthalmol. 1964 Jun;3:266-72.
10
ION TRANSPORT IN ISOLATED RABBIT ILEUM. I. SHORT-CIRCUIT CURRENT AND NA FLUXES.离体兔回肠中的离子转运。I. 短路电流与钠通量
J Gen Physiol. 1964 Jan;47(3):567-84. doi: 10.1085/jgp.47.3.567.

阳离子、阴离子和碳酸酐酶在兔角膜内皮液体转运中的作用。

Role of cations, anions and carbonic anhydrase in fluid transport across rabbit corneal endothelium.

作者信息

Fischbarg J, Lim J J

出版信息

J Physiol. 1974 Sep;241(3):647-75. doi: 10.1113/jphysiol.1974.sp010676.

DOI:10.1113/jphysiol.1974.sp010676
PMID:4215880
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1331055/
Abstract
  1. A small electrical potential difference (541 +/- 48 muV, aqueous side negative) across rabbit corneal endothelium has been recently found. Its dependence on ambient [Na(+)], [K(+)], [H(+)] and metabolic and specific inhibitors was examined.2. Changes in concentration of the ions above either were known or were presently shown to affect the rate of fluid transport across this preparation (normal value: 5.2 +/- 0.4 mul./hr.cm(2)). Ionic concentration changes were also found here to influence potential difference in the same way as fluid transport. In the cases tested, the effects on both fluid transport and potential difference were reversible.3. Fluid transport and potential difference were both decreased or abolished in absence of Na(+), K(+) and HCO(3) (-), and when [H(+)] was decreased. Fluid transport and potential difference were saturable functions of [HCO(3) (-)] and half-saturation occurred in both cases at about 13 mM-HCO(3) (-). The potential difference was also a saturable function of [Na(+)] (half-saturation around 15 mM). There was a pH optimum for potential difference in the range 7.4-7.6. Lower pH values decreases the potential difference and the fluid transport, and a small (-100 muV) reversed potential was observed in the range of 5.3-5.5.4. Total replacement of Cl(-) by HCO(3) (-) or SO(4) (2-) produced no impairment on either fluid transport or potential difference.5. Carbonic anhydrase inhibitors (ethoxyzolamide 10(-5) or 10(-4)M and benzolamide 10(-3)M) produced a 40-60% decrease in the rate of fluid pumping. In contrast, ethoxyzolamide 10(-4)M or acetazolamide 10(-3)M did not produce any change in the potential difference. NaCN and Na iodoacetate (both 2 mM) eliminated the potential difference in 1-1.5 hr while in controls it lasted for 5-6 hr.6. Ouabain (10(-5)M) abolished the potential difference in less than 10 sec when added to the aqueous side, which suggests the existence of an electrogenic pump. This extremely fast time transient can be accounted for by the accessibility and simple geometry of the present monocellular layer. Ouabain abolished also the reversed potential difference observed at low pH.7. The data are interpreted in terms of a scheme similar to that advanced for other epithelia and in which (a) H(+) would be pumped into the intercellular spaces, while Na(+) and CO(2) would enter into the cells, and (b) Na(+) would be subsequently pumped into the aqueous humour, producing as a result the fluid movement observed. The actual origin of the potential difference is further discussed in terms of two contrasting possibilities: (i) one or more electrogenic pumps, and (ii) a neutral pump which would create a diffusion potential across ;leaky' intercellular junctions.
摘要
  1. 最近发现兔角膜内皮存在一个小的电势差(541±48微伏,水相侧为负)。研究了其对环境中[Na⁺]、[K⁺]、[H⁺]以及代谢和特异性抑制剂的依赖性。

  2. 上述离子浓度的变化已知或目前已表明会影响通过该标本的液体转运速率(正常值:5.2±0.4微升/小时·平方厘米)。在此还发现离子浓度变化以与液体转运相同的方式影响电势差。在测试的情况下,对液体转运和电势差的影响都是可逆的。

  3. 在无Na⁺、K⁺和HCO₃⁻以及[H⁺]降低时,液体转运和电势差均降低或消失。液体转运和电势差是[HCO₃⁻]的饱和函数,两种情况下半饱和均出现在约13毫摩尔/升HCO₃⁻时。电势差也是[Na⁺]的饱和函数(半饱和约在15毫摩尔/升)。电势差在7.4 - 7.6范围内存在最适pH值。较低的pH值会降低电势差和液体转运,在5.3 - 5.5范围内观察到一个小的(-100微伏)反向电势。

  4. 用HCO₃⁻或SO₄²⁻完全替代Cl⁻对液体转运或电势差均无损害。

  5. 碳酸酐酶抑制剂(乙氧唑胺10⁻⁵或10⁻⁴摩尔/升以及苯唑胺10⁻³摩尔/升)使液体泵浦速率降低40 - 60%。相比之下,乙氧唑胺10⁻⁴摩尔/升或乙酰唑胺10⁻³摩尔/升对电势差无任何影响。NaCN和碘代乙酸钠(均为2毫摩尔)在1 - 1.5小时内消除电势差,而在对照中其持续5 - 6小时。

  6. 哇巴因(10⁻⁵摩尔/升)添加到水相侧时在不到10秒内消除电势差,这表明存在一个生电泵。这种极快的时间瞬变可由当前单细胞层的可及性和简单几何结构来解释。哇巴因也消除了在低pH时观察到的反向电势差。

  7. 数据按照与其他上皮组织提出的类似模式进行解释,其中(a)H⁺被泵入细胞间隙,而Na⁺和CO₂进入细胞,(b)随后Na⁺被泵入水液,从而产生观察到的液体流动。电势差的实际起源根据两种相反的可能性进一步讨论:(i)一个或多个生电泵,以及(ii)一个中性泵,它会在“渗漏”的细胞间连接上产生扩散电势。