首页> 美国卫生研究院文献>The Journal of Physiology >Interstitial PCO2 and pH and their role as chemostimulants in the isolated respiratory network of neonatal rats.
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Interstitial PCO2 and pH and their role as chemostimulants in the isolated respiratory network of neonatal rats.

机译:间质性PCO2和pH值以及它们在新生大鼠孤立的呼吸网络中作为化学刺激剂的作用。

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摘要

1. CO2-H(+)-sensitive microelectrodes were used for simultaneous measurements of the partial pressure of CO2 (PCO2) and extracellular pH (pHo) in the ventral respiratory group (VRG) of the isolated brainstem-spinal cord of neonatal rats. Some of the data were analysed using diffusion equations. 2. With increasing recording depth within the boundaries of the VRG (300-600 microns below the tissue surface), PCO2 increased from 77 to 95 mmHg and pHo fell from 7.0 to 6.8 at steady state in standard saline equilibrated with 5% CO2 and 95% O2. 3. Elevating bath CO2 from 5 to 10-12.5% produced a mean increase in PCO2 of 18 mmHg, a fall in pHo of 0.13 pH units, and a 50-250% increase in the frequency of respiration-related spinal (C2) nerve bursts. Similar effects on C2 activity and pHo were observed upon lowering bath [HCO3-] from 25 to 10 mM, leading to a mean decrease in PCO2 of 4.4 mmHg in the VRG. 4. Raising bath [HCO3-] to 50 mM produced a substantial frequency decrease, a rise in pHo of 0.24 pH units and an elevation in PCO2 of 9.3 mmHg. C2 activity was not profoundly affected upon doubling the CO2-HCO3- content, leading to a mean increase in pHo of 0.13 pH units and elevation of PCO2 by 30 mmHg. 5. In a CO2-HCO3(-)-free, Hepes-buffered solution, PCO2 decreased to 18 mmHg in the VRG and pHo fell by 0.15 pH units with no major effect on rhythmic activity. Subsequent anoxic exposure for more than 15 min produced a further fall in PCO2 to below 1 mmHg, a decrease in pHo of 0.55 pH units, and blockade of respiration-related activity. In three out of the six preparations tested, C2 activity could be restored by reapplication of CO2-HCO3- in the absence of O2. 6. C2 activity persisted at a reduced frequency, even up to 30 min, during anoxia in the CO2-HCO(-)-buffered saline,leading to an elevation in PCO2 of 15 mmHg and a fall in pHo of 0.18 pH units. 7. The diffusion coefficient of CO2 in the tissue was found to be equal to that in saline. Two mean estimates for anoxic tissue of the function lambda 2/ alpha of tortuosity (lambda) and extracellular volume fraction (alpha), affecting extracellular diffusion of bicarbonate, were 4.7 and 4.1. The mean rate of acid production by anoxic tissue was 1.1 mequiv 1-1 min-1. 8. The results suggest that extracellular H+ is the primary stimulating factor in central chemosensitivity, which may often mask the less evident effects of CO2. A model of diffusion of acid equivalents in brain tissue is proposed.
机译:1. CO2-H(+)敏感的微电极用于同时测量新生大鼠离体脑干-脊髓的腹侧呼吸组(VRG)中的CO2分压(PCO2)和细胞外pH(pHo)。使用扩散方程分析了一些数据。 2.随着VRG边界(组织表面以下300-600微米)内记录深度的增加,在用5%CO2和95平衡的标准盐水中,稳态下PCO2从77 mmHg增加到95 mmHg,pHo从7.0下降到6.8。 %O2。 3.将浴中的CO2从5提高到10-12.5%可使PCO2平均增加18 mmHg,pHo下降0.13 pH单位,呼吸相关脊柱(C2)神经频率增加50-250%爆发。将浴液[HCO3-]从25 mM降低至10 mg,可观察到对C2活性和pHo的类似影响,从而导致VRG中的PCO2平均降低4.4 mmHg。 4.将浴液[HCO3-]升高至50 mM,频率会大幅降低,pHo升高0.24 pH单位,PCO2升高9.3 mmHg。将CO2-HCO3-含量加倍后,对C2的活性影响不大,导致pHo平均增加0.13 pH单位,PCO2升高30 mmHg。 5.在不含CO2-HCO3(-)的Hepes缓冲溶液中,VRG中的PCO2降至18 mmHg,pHo下降0.15个pH单位,对韵律活性没有重大影响。随后缺氧暴露超过15分钟会导致PCO2进一步下降至1 mmHg以下,pHo降低0.55 pH单位,并阻止呼吸相关活性。在所测试的六种制剂中,有三种可以通过在没有O2的情况下重新施用CO2-HCO3-来恢复C2活性。 6.在CO2-HCO(-)缓冲盐水中缺氧期间,C2活性持续降低的频率,甚至长达30分钟,导致PCO2升高15 mmHg,pHo降低0.18 pH单位。 7.发现CO 2在组织中的扩散系数等于在盐水中的扩散系数。缺氧组织的功能λ2/曲折度α(lambda)和细胞外体积分数(α)的缺氧组织的平均估计值分别为4.7和4.1,影响碳酸氢根的细胞外扩散。缺氧组织产生酸的平均速率为1.1 mequiv 1-1 min-1。 8.结果表明,细胞外H +是中枢化学敏感性的主要刺激因素,这通常可能掩盖了CO2不太明显的作用。提出了当量酸在脑组织中扩散的模型。

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