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一项以佛波醇二丁酸酯为探针,对藤壶肌纤维中哇巴因不敏感钠外流的研究。

A study of the ouabain-insensitive sodium efflux in barnacle muscle fibres using phorbol dibutyrate as a probe.

作者信息

Bittar E E, Nwoga J

机构信息

Department of Physiology, University of Wisconsin, Madison 53706.

出版信息

J Physiol. 1990 May;424:263-82. doi: 10.1113/jphysiol.1990.sp018066.

Abstract
  1. The resting ouabain-insensitive Na+ efflux in muscle fibres isolated from the barnacle, Balanus nubilus, is stimulated by external or internal application of phorbol 12,13-dibutyrate (PD). The response occurs fairly promptly and may not decay at all, or more commonly, decay rather slowly. The magnitude of the response to external or internal application of PD is dose-dependent, the minimum effective concentration being about 10(-8) M. 2. The response to PD fails to occur in the nominal absence of external Ca2+. Sudden removal of external Ca subsequent to peak stimulation by PD leads to almost complete reversal of the response. The response to PD of fibres suspended in Li(+)-ASW (artificial sea water) is similar in magnitude to that of fibres suspended in Na(+)-ASW. However, it differs in that it is of a sustained nature. 3. Calcium channel blockers, e.g. verapamil, completely prevent the response to PD from occurring. Both Cd2+ and Co2+ are less effective than verapamil. 4. Pre- but not post-injection of EGTA reduces the response to PD. Pre- or post-injection of Mg2+ reduces the response considerably. 5. Fibres pre-injected with GTP show a reduced response to PD. Fibres pre-injected with PD show a reduced response to GTP. Pre-injection of protein kinase inhibitor is without effect on the response to PD. 6. Furosemide, piretanide and bumetanide are without effect on the response to PD. 7. DIDS (4,4'-diisothiocyanostilbene-2,2-disulphonic acid) is a potent inhibitor of the response to PD but not amiloride. Pyridoxal 5-phosphate and benzolamide are also powerful inhibitors. Pyridoxal 5-phosphate in combination with benzolamide fails to completely abolish or reverse the response to PD. 8. Luminescence from aequorin is promptly increased by PD in a dose-dependent manner, the minimal effective concentration being in the nanomolar range. The signal is monophasic or multiphasic in shape, and is often less than 5 min in duration. Not infrequently, however, the aequorin response fails to completely decay and the new level of resting glow remains above the original baseline level. 9. Collectively, these observations accord with a tentative general hypothesis stating that the stimulatory response of the ouabain-insensitive Na+ efflux to PD is triggered by two mechanisms. One involves a rise in myoplasmic free [Ca2+] resulting from the entry of external Ca2+ via opened Ca2+ channels which is followed by the operation of the Na(+)-Ca2+ exchanger in the reverse mode.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 从藤壶(Balanus nubilus)分离出的肌肉纤维中,静息状态下对哇巴因不敏感的钠外流,可被细胞外或细胞内施加佛波醇12,13 - 二丁酸酯(PD)所刺激。该反应相当迅速地发生,并且可能根本不衰减,或者更常见的是衰减相当缓慢。对细胞外或细胞内施加PD的反应幅度呈剂量依赖性,最小有效浓度约为10^(-8)M。2. 在名义上无细胞外钙的情况下,对PD的反应不会发生。在PD达到峰值刺激后突然去除细胞外钙,几乎会导致反应完全逆转。悬浮在锂人工海水(Li(+)-ASW)中的纤维对PD的反应幅度与悬浮在钠人工海水(Na(+)-ASW)中的纤维相似。然而,不同之处在于它具有持续的性质。3. 钙通道阻滞剂,如维拉帕米,完全阻止对PD的反应发生。镉离子(Cd2+)和钴离子(Co2+)的效果比维拉帕米差。4. 注射乙二醇双四乙酸(EGTA)前而非注射后会降低对PD的反应。注射镁离子(Mg2+)前或后会显著降低反应。5. 预先注射鸟苷三磷酸(GTP)的纤维对PD的反应降低。预先注射PD的纤维对GTP的反应降低。预先注射蛋白激酶抑制剂对PD的反应没有影响。6. 速尿、吡咯他尼和布美他尼对PD的反应没有影响。7. 4,4'-二异硫氰基芪-2,2-二磺酸(DIDS)是对PD反应的有效抑制剂,但氨氯地平不是。磷酸吡哆醛和苯并酰胺也是强效抑制剂。磷酸吡哆醛与苯并酰胺联合使用不能完全消除或逆转对PD的反应。8. 水母发光蛋白的发光会被PD迅速以剂量依赖性方式增强,最小有效浓度在纳摩尔范围内。信号形状为单相或多相,持续时间通常小于5分钟。然而,水母发光蛋白的反应常常不能完全衰减,新的静息发光水平仍高于原始基线水平。9. 总体而言,这些观察结果符合一个初步的一般假设,即对哇巴因不敏感的钠外流对PD的刺激反应由两种机制触发。一种机制涉及细胞外钙通过开放的钙通道进入导致肌浆游离钙离子浓度升高,随后钠钙交换体以反向模式运作。(摘要截选至400字)

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Chloride efflux in single barnacle muscle fibres.藤壶单根肌纤维中的氯离子外流
J Physiol. 1980 Apr;301:317-36. doi: 10.1113/jphysiol.1980.sp013208.
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Measurement of Ca2+ concentrations in living cells.活细胞中钙离子浓度的测量。
Prog Biophys Mol Biol. 1982;40(1-2):1-114. doi: 10.1016/0079-6107(82)90011-6.

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