THE LIBERATION OF ADENOSINE TRIPHOSPHATE ON ANTIDROMIC STIMULATION OF SENSORY NERVES
THE LIBERATION OF ADENOSINE TRIPHOSPHATE ON ANTIDROMIC STIMULATION OF SENSORY NERVES
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DOI:
10.1113/jphysiol.1959.sp006157
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发表时间:
1959-01-01
影响因子:
5.5
通讯作者:
HOLTON, P
中科院分区:
文献类型:
--
作者:
HOLTON, P
METHODS Perfusion method Rabbits' ears were perfused by Rischbieter's (1913) method at pressures from 40 to 200 mm Hg to obtain a suitable rate of flow of perfusion fluid (0-05-1 ml./min). The dissection was carried out under urethane anaesthesia and care was taken that the blood flow through the ear was stopped for as short a time as possible, usually less than 2 min, before the perfusion was established. In most experiments the perfusion fluid was 6% dextran (Intradex, Glaxo Ltd. or Dextraven, Benger Laboratories Ltd.) to which salts were added to give the composition of Locke's solution (NaCl 9, KCI 0* 4, CaCl2 0x24, NaHCO3 0.5, glucose1. 0 g/l.) and a pH of 7* 3-7-4 after equilibration with oxygen containing 5% CO2. In a few experiments Locke's solution without dextran was used and similar results were obtained, but the ear became oedematous after a few hours' perfusion.The perfusion was at room temperature. The venous effluent was collected in centrifuge tubes surrounded by crushed ice and was kept cool until it was tested. It was centrifuged for 5 min to sediment the erythrocytes which were washed out of the tissues, and the supernatant was used for analysis.