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鸟嘌呤核苷酸和环核苷酸对兔门静脉单个膜片钳平滑肌细胞钙储备的作用

Actions of guanine nucleotides and cyclic nucleotides on calcium stores in single patch-clamped smooth muscle cells from rabbit portal vein.

作者信息

Komori S, Bolton T B

机构信息

Department of Pharmacology and Clinical Pharmacology, St George's Hospital Medical School, London.

出版信息

Br J Pharmacol. 1989 Jul;97(3):973-82. doi: 10.1111/j.1476-5381.1989.tb12039.x.

Abstract
  1. Single smooth muscle cells were obtained from the rabbit portal vein by enzymic digestion and membrane currents under voltage clamp measured by whole-cell patch clamp technique. 2. When held at depolarized potentials, spontaneous outward currents (STOCs) were discharged; it is likely that these represent the cyclical storage and release within the cell of calcium in relation to Ca-activated K-channels. 3. Application of lower concentrations of carbachol (10(-5)M) or caffeine (10(-3)M) accelerated STOC discharge. Higher concentrations of caffeine (10(-2)M) or carbachol (10(-4)M), or noradrenaline (10(-5)M), produced an outward current of 1-5 nA which disappeared within 5-15s and which was considered to result from the discharge of calcium stores; STOC discharge was abolished for a period. 4. Ryanodine (10(-5)-10(-4)M) or a non-hydrolysable GTP analogue, GTP gamma S (10(-5)-10(-3)M) introduced into the cell abolished STOC discharge within 2-5 min. STOCs were large in cells filled with GDP beta S (10(-3)M) and the action of GTP gamma S introduced at various concentrations was antagonized. 5. GTP gamma S (10(-4)-10(-3)M) in the cell reduced or abolished outward current to caffeine (10(-2)M) noradrenaline (10(-5)M) or carbachol (10(-4)M); the effect on caffeine outward current was antagonized by GDP beta S (10(-3)M) introduced into the cell. GDP beta S reduced noradrenaline outward current but not caffeine outward current implying the existence of a G-protein step in noradrenaline-evoked Ca-store release, possibly regulating phospholipase C enzyme activity and D-myo inositol 1,4,5 trisphosphate formation. 6. If cyclic AMP (10(-3)M) or cyclic GMP (10(-3)M) was introduced into the cell, or 8-bromo cyclic AMP (0.5 x 10(-3)M) or 8-bromo cyclic GMP (0.5 x 10(-3)M) applied to the cell in the bathing solution, STOC discharge was only slightly affected. However, the outward current to caffeine applied after noradrenaline was much enhanced. 7. The results could be explained if cyclic GMP and cyclic AMP enhance calcium storage whereas GTP gamma S depletes calcium stores, an action antagonized by GDP beta S.
摘要
  1. 通过酶消化从兔门静脉获取单个平滑肌细胞,并采用全细胞膜片钳技术在电压钳制下测量膜电流。2. 当保持在去极化电位时,会释放出自发性外向电流(STOCs);这些电流很可能代表细胞内钙与钙激活钾通道相关的周期性储存和释放。3. 施加较低浓度的卡巴胆碱(10⁻⁵M)或咖啡因(10⁻³M)会加速STOC放电。较高浓度的咖啡因(10⁻²M)或卡巴胆碱(10⁻⁴M),或去甲肾上腺素(10⁻⁵M),会产生1 - 5 nA的外向电流,该电流在5 - 15秒内消失,被认为是钙储存释放的结果;STOC放电会在一段时间内被消除。4. 引入细胞内的ryanodine(10⁻⁵ - 10⁻⁴M)或一种不可水解的GTP类似物GTPγS(10⁻⁵ - 10⁻³M)会在2 - 5分钟内消除STOC放电。充满GDPβS(10⁻³M)的细胞中的STOC较大,且不同浓度引入的GTPγS的作用会被拮抗。5. 细胞内的GTPγS(10⁻⁴ - 10⁻³M)会减少或消除对咖啡因(10⁻²M)、去甲肾上腺素(10⁻⁵M)或卡巴胆碱(10⁻⁴M)的外向电流;对咖啡因外向电流的影响会被引入细胞内的GDPβS(10⁻³M)拮抗。GDPβS会减少去甲肾上腺素外向电流,但不会减少咖啡因外向电流,这意味着在去甲肾上腺素诱发的钙储存释放中存在一个G蛋白步骤,可能调节磷脂酶C酶活性和D - 肌醇1,4,5 - 三磷酸的形成。6. 如果将环磷酸腺苷(10⁻³M)或环磷酸鸟苷(10⁻³M)引入细胞,或者在浴液中向细胞施加8 - 溴环磷酸腺苷(0.5×10⁻³M)或8 - 溴环磷酸鸟苷(0.5×10⁻³M),STOC放电只会受到轻微影响。然而,去甲肾上腺素后施加的咖啡因的外向电流会大大增强。7. 如果环磷酸鸟苷和环磷酸腺苷增强钙储存而GTPγS耗尽钙储存,且该作用被GDPβS拮抗,那么这些结果就可以得到解释。

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G proteins: a family of signal transducers.G蛋白:一类信号转导分子家族。
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