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本文引用的文献

1
Some properties of the external activation site of the sodium pump in crab nerve.蟹神经中钠泵外部激活位点的一些特性
J Physiol. 1966 Jul;185(2):270-97. doi: 10.1113/jphysiol.1966.sp007987.
2
On the permeability of mammalian non-myelinated fibres to sodium and to lithium ions.关于哺乳动物无髓鞘纤维对钠离子和锂离子的通透性
J Physiol. 1963 Jan;165(1):130-40. doi: 10.1113/jphysiol.1963.sp007047.
3
Potassium movement in relation to nerve activity.与神经活动相关的钾离子移动。
J Gen Physiol. 1951 Jul;34(6):795-807. doi: 10.1085/jgp.34.6.795.
4
The permeability of frog muscle fibres to lithium ions.蛙肌纤维对锂离子的通透性。
J Physiol. 1959 Oct;147(3):626-38. doi: 10.1113/jphysiol.1959.sp006265.
5
Active transport of cations in giant axons from Sepia and Loligo.乌贼和枪乌贼巨大轴突中阳离子的主动运输。
J Physiol. 1955 Apr 28;128(1):28-60. doi: 10.1113/jphysiol.1955.sp005290.
6
THE INITIAL HEAT PRODUCTION ASSOCIATED WITH THE NERVE IMPULSE IN CRUSTACEAN AND MAMMALIAN NON-MYELINATED NERVE FIBRES.甲壳类动物和哺乳动物无髓神经纤维中与神经冲动相关的初始产热
J Physiol. 1965 May;178(2):368-83. doi: 10.1113/jphysiol.1965.sp007633.
7
AN ANALYSIS OF THE TRANSVERSE ELECTRICAL IMPEDANCE OF STRIATED MUSCLE.横纹肌横向电阻抗分析
Proc R Soc Lond B Biol Sci. 1964 Mar 17;159:606-51. doi: 10.1098/rspb.1964.0023.
8
Effect of frequency of electrical stimulation on the concentration of intermediary metabolites in mammalian non-myelinated fibres.电刺激频率对哺乳动物无髓鞘纤维中中间代谢产物浓度的影响。
J Physiol. 1959 Oct;148(2):353-61. doi: 10.1113/jphysiol.1959.sp006292.
9
Restoration by barium of action potentials in sodium-deprived mammalian B and C fibres.钡对缺钠的哺乳动物B类和C类纤维动作电位的恢复作用。
J Physiol. 1959 Mar 12;145(3):562-9. doi: 10.1113/jphysiol.1959.sp006162.
10
After-potentials in mammalian non-myelinated nerve fibres.哺乳动物无髓神经纤维的后电位。
J Physiol. 1958 Dec 30;144(3):442-62. doi: 10.1113/jphysiol.1958.sp006112.

哺乳动物无髓神经纤维中单个冲动相关的初始热的起源。

The origin of the initial heat associated with a single impulse in mammalian non-myelinated nerve fibres.

作者信息

Howarth J V, Keynes R D, Ritchie J M

出版信息

J Physiol. 1968 Feb;194(3):745-93. doi: 10.1113/jphysiol.1968.sp008434.

DOI:10.1113/jphysiol.1968.sp008434
PMID:5636997
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1365662/
Abstract
  1. A study has been made of the temperature changes associated with the passage of a single impulse in rabbit desheated vagus nerves.2. The initial changes consist of an evolution of positive heat followed by a reabsorption of most of it; i.e. there is a phase of positive and a phase of negative heat production.3. The size of the positive heat, its time of onset, and the time of onset of the negative heat have been measured by an analogue method of analysis. In addition, these parameters, together with the size of the negative heat and the duration of both phases of initial heat, have been studied with the aid of a computer, and also by conventional heat block analysis.4. At about 5 degrees C the measured positive heat is 7.2 mucal/g. impulse. It starts as soon as the compound action potential reaches the thermopile and lasts for about 107 msec.5. This positive heat decreases with increasing temperature, the ratio of heat at 4 degrees C to that at 14 degrees C being 1.86.6. The measured negative heat at about 5 degrees C is 4.9 mucal/g. impulse. It starts 102 msec after the onset of positive heat, and lasts for about 240 msec.7. When the sodium of Locke solution is replaced by lithium the positive heat is reduced by 19%, but the negative heat is increased by 22%.8. In potassium-free solutions the positive heat is hardly affected (increase of 5%), but the negative heat is more than doubled. As a result the nerve may become briefly colder than its initial temperature by about 2 mu degrees C.9. The effect of sodium-deficient solutions on the positive heat is somewhat variable, but the negative heat is consistently diminished.10. Replacement of the chloride of Locke solution by sulphate or nitrate has little effect on the positive heat. The negative heat is reduced in size by 26% and in duration by 22%.11. Replacement of most of the sodium of Locke solution by barium reduces or abolishes the negative heat, and increases the measured size of the positive heat nearly threefold.12. Veratrine (10(-5) g/ml.) produces a nearly tenfold increase in the net positive heat.13. Ouabain (1 mM) and antimycin A (1 mug/ml.) applied for 30-60 min have little effect on the initial heat production.14. Over the temperature range 5-15 degrees C, and for the ionic solution changes described above, there is close agreement in timing between the positive heat and the rising phase of the action potential, and between the negative heat and the falling phase.15. Because of the inevitable temporal dispersion of the action potential over the face of the thermopile, the observed temperature changes are smaller than those which occur at a single point in the nerve close to a stimulating electrode. The corrected value of the positive heat at 5 degrees C is 24.5 mucal/g. impulse, while that of the negative heat is 22.2 mucal/g. impulse.16. The heats of mixing of the ions in solution that interchange during the action potential are much too small to account for the observed initial heats, but an exchange of ions associated with fixed charges might make a significant contribution to the heats.17. The condenser theory, according to which the positive heat represents the dissipation of electrical energy stored in the membrane capacity, while the negative heat results from the recharging of the capacity, appears unable to account for more than half of the observed temperature changes.18. It seems probable that the greater part of the initial heat results from changes in the entropy of the nerve membrane when it is depolarized and repolarized.
摘要
  1. 已对家兔失温迷走神经中单个冲动通过时伴随的温度变化进行了研究。

  2. 最初的变化包括产生正热,随后大部分正热又被重新吸收;即存在一个正热产生阶段和一个负热产生阶段。

  3. 正热的大小、其起始时间以及负热的起始时间已通过一种模拟分析方法进行了测量。此外,借助计算机以及传统的热阻分析,对这些参数以及负热的大小和初始热两个阶段的持续时间进行了研究。

  4. 在约5℃时,测得的正热为7.2微卡/克·冲动。一旦复合动作电位到达热电堆,它就开始出现,并持续约107毫秒。

  5. 这种正热随温度升高而降低,4℃时的热与14℃时的热之比为1.86。

  6. 在约5℃时测得的负热为4.9微卡/克·冲动。它在正热开始后102毫秒开始,并持续约240毫秒。

  7. 当洛克溶液中的钠被锂取代时,正热减少19%,但负热增加22%。

  8. 在无钾溶液中,正热几乎不受影响(增加5%),但负热增加了一倍多。结果,神经可能会比其初始温度短暂低约2微摄氏度。

  9. 缺钠溶液对正热的影响有些变化,但负热持续减少。

  10. 用硫酸盐或硝酸盐取代洛克溶液中的氯化物对正热影响不大。负热的大小减少26%,持续时间减少22%。

  11. 用钡取代洛克溶液中的大部分钠会减少或消除负热,并使测得的正热大小增加近三倍。

  12. 藜芦碱(10⁻⁵克/毫升)使净正热增加近十倍。

  13. 哇巴因(1毫摩尔)和抗霉素A(1微克/毫升)作用30 - 60分钟对初始产热影响不大。

  14. 在5 - 15℃的温度范围内,对于上述离子溶液变化,正热与动作电位上升相之间以及负热与动作电位下降相之间在时间上密切一致。

  15. 由于动作电位在热电堆表面不可避免地存在时间离散,观察到的温度变化小于在靠近刺激电极的神经单点处发生的温度变化。5℃时正热的校正值为24.5微卡/克·冲动,而负热的校正值为22.2微卡/克·冲动。

  16. 动作电位期间溶液中相互交换的离子的混合热太小,无法解释观察到的初始热,但与固定电荷相关的离子交换可能对热有显著贡献。

  17. 电容理论认为正热代表膜电容中储存的电能的耗散,而负热是电容再充电的结果,似乎只能解释不到一半的观察到的温度变化。

  18. 很可能大部分初始热是神经膜去极化和复极化时熵变化的结果。