首页> 美国卫生研究院文献>The Journal of Physiology >Autoregulation of renal blood flow in the conscious dog and the contribution of the tubuloglomerular feedback
【2h】

Autoregulation of renal blood flow in the conscious dog and the contribution of the tubuloglomerular feedback

机译:自觉狗肾血流量的自动调节和肾小管肾小球反馈的作用

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

class="enumerated" style="list-style-type:decimal">The aim of this study was to investigate the autoregulation of renal blood flow under physiological conditions, when challenged by the normal pressure fluctuations, and the contribution of the tubuloglomerular feedback (TGF).The transfer function between 0.0018 and 0.5 Hz was calculated from the spontaneous fluctuations in renal arterial blood pressure (RABP) and renal blood flow (RBF) in conscious resting dogs. The response of RBF to stepwise artificially induced reductions in RABP was also studied (stepwise autoregulation).Under control conditions (n = 12 dogs), the gain of the transfer function started to decrease, indicating improving autoregulation, below 0.06-0.15 Hz (t = 7-17 s). At 0.027 Hz a prominent peak of high gain was found. Below 0.01 Hz (t > 100 s), the gain reached a minimum (maximal autoregulation) of -6.3 ± 0.6 dB. The stepwise autoregulation (n = 4) was much stronger (-19.5 dB). The time delay of the transfer function was remarkably constant from 0.03 to 0.08 Hz (high frequency (HF) range) at 1.7 s and from 0.0034 to 0.01 Hz (low frequency (LF) range) at 14.3 s, respectively.Nifedipine, infused into the renal artery, abolished the stepwise autoregulation (-2.0 ± 1.1 dB, n = 3). The gain of the transfer function (n = 4) remained high down to 0.0034 Hz; in the LF range it was higher than in the control (0.3 ± 1.0 dB, P < 0.05). The time delay in the HF range was reduced to 0.5 s (P < 0.05).After ganglionic blockade (n = 7) no major changes in the transfer function were observed.Under furosemide (frusemide) (40 mg + 10 mg h−1 or 300 mg + 300 mg h−1 i.v.) the stepwise autoregulation was impaired to -7.8 ± 0.3 or -6.7 ± 1.9 dB, respectively (n = 4). In the transfer function (n = 7 or n = 4) the peak at 0.027 Hz was abolished. The delay in the LF range was reduced to -1.1 or -1.6 s, respectively. The transfer gain in the LF range (-5.5 ± 1.2 or -3.8 ± 0.8 dB, respectively) did not differ from the control but was smaller than that under nifedipine (P < 0.05).It is concluded that the ample capacity for regulation of RBF is only partially employed under physiological conditions. The abolition by nifedipine and the negligible effect of ganglionic blockade show that above 0.0034 Hz it is almost exclusively due to autoregulation by the kidney itself. TGF contributes to the maximum autoregulatory capacity, but it is not required for the level of autoregulation expended under physiological conditions. Around 0.027 Hz, TGF even reduces the degree of autoregulation.
机译:class =“ enumerated” style =“ list-style-type:decimal”> <!-list-behavior =枚举前缀-word = mark-type = decimal max-label-size = 0-> 这项研究的目的是研究在正常压力波动的挑战下,生理条件下肾血流量的自动调节以及肾小管肾小球反馈(TGF)的作用。 0.0018至从有意识的静息狗的肾动脉血压(RABP)和肾血流量(RBF)的自发波动中计算出0.5 Hz。还研究了RBF对人为引起的RABP逐步降低的反应(逐步自动调节)。 在控制条件下(n = 12只狗),传递函数的增益开始降低,表明自动调节得到改善,低于0.06-0.15 Hz(t = 7-17 s)。在0.027 Hz处,发现了一个明显的高增益峰值。低于0.01 Hz(t> 100 s),增益达到-6.3±0.6 dB的最小值(最大自动调节)。逐步自动调节(n = 4)要强得多(-19.5 dB)。传递函数的时间延迟在1.7 s时分别从0.03到0.08 Hz(高频(HF)范围)和在14.3 s时从0.0034到0.01 Hz(低频(LF)范围)显着恒定。注入肾动脉的硝苯地平取消了逐步自律调节(-2.0±1.1 dB,n = 3)。传递函数的增益(n = 4)保持高至0.0034 Hz。在LF范围内,它高于对照组(0.3±1.0 dB,P <0.05)。在HF范围内的时间延迟减少到0.5 s(P <0.05)。 在神经节阻滞(n = 7)后,没有观察到传递函数的重大变化。 在呋塞米(呋塞米)(40 mg + 10 mg h -1 或300 mg + 300 mg h -1 iv)下,逐步自动调节被削弱至-7.8±0.3或分别为-6.7±1.9 dB(n = 4)。在传递函数(n = 7或n = 4)中,消除了0.027 Hz处的峰值。 LF范围中的延迟分别降低到-1.1或-1.6 s。 LF范围内的转移增益(分别为-5.5±1.2或-3.8±0.8 dB)与对照无差异,但比硝苯地平下的转移增益小(P <0.05)。 结论是充分调节RBF的能力仅在生理条件下被部分利用。硝苯地平的废除和神经节阻滞作用的影响可忽略不计,表明0.0034 Hz以上几乎完全归因于肾脏自身的自我调节。 TGF有助于最大的自动调节能力,但在生理条件下消耗的自动调节水平并不是必需的。约0.027 Hz时,TGF甚至会降低自调节的程度。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号