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关于G蛋白激活和磷酸化在豚鼠心房细胞对乙酰胆碱脱敏中的作用

On the role of G protein activation and phosphorylation in desensitization to acetylcholine in guinea-pig atrial cells.

作者信息

Zang W J, Yu X J, Honjo H, Kirby M S, Boyett M R

机构信息

Department of Physiology, University of Leeds.

出版信息

J Physiol. 1993 May;464:649-79. doi: 10.1113/jphysiol.1993.sp019656.

Abstract
  1. The ACh-activated K+ current (IK,ACh) has been investigated in guinea-pig atrial cells at 36 degrees C using the whole-cell patch-clamp technique. 2. During an exposure to ACh, IK,ACh faded as a result of desensitization. Throughout the fade of the current, the current reversed at EK and showed inward-going rectification. The fade was, therefore, the result of a genuine decrease in IK,ACh. 3. The onset of desensitization (as judged by the fade of IK,ACh) was biphasic and the time constants of the fast and slow phases of desensitization were 1.58 +/- 0.14 (n = 16) and 148.2 +/- 12.8 s (n = 18) respectively. Recovery from the fast and slow phases of desensitization (after 30 s and 5 min exposures to ACh respectively) occurred with time constants of 52 and 222 s respectively. This suggests that two processes are involved in desensitization. 4. The Q10 of the rate constant of the fast phase of desensitization was 2.2 +/- 0.3 (n = 6). 5. Intracellular perfusion with guanosine 5'-O-(3-thiotriphosphate) (GTP gamma S) or extracellular perfusion with AlF4- were used to bypass the muscarinic receptor and trigger IK,ACh by directly activating the G protein, GK, that links the muscarinic receptor to the K+ channel. Both GTP gamma S and AlF4- activated a current with the same reversal potential and the same degree of inward-going rectification as the ACh-activated current. 6. Desensitization still occurred when the muscarinic receptor was bypassed and IK,ACh was triggered by direct activation of GK with either GTP gamma S or AlF4-. This suggests that desensitization is, in part, the result of a modification of either GK or the K+ channel. 7. Activation of the muscarinic receptor by ACh resulted in greater desensitization than direct activation of GK; at the end of a 5 min exposure to ACh, current was only 22 +/- 1% (n = 19) of its peak value, whereas, after direct activation of GK by GTP gamma S for 5 min, current was 42 +/- 6% (n = 5) of its peak value. This suggests that desensitization also involves the muscarinic receptor. 8. When cells were perfused with GTP gamma S, the fast phase of desensitization could still occur, but the slow phase was reduced. This suggests that the fast phase involves GK or the K+ channel, whereas the slow phase involves the muscarinic receptor.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 采用全细胞膜片钳技术,在36℃下对豚鼠心房细胞中的乙酰胆碱激活钾电流(IK,ACh)进行了研究。2. 在暴露于乙酰胆碱的过程中,IK,ACh因脱敏作用而衰减。在电流衰减过程中,电流在EK处反转,并表现出内向整流。因此,这种衰减是IK,ACh真正减少的结果。3. 脱敏作用的起始(通过IK,ACh的衰减判断)是双相的,脱敏作用快速相和慢速相的时间常数分别为1.58±0.14(n = 16)和148.2±12.8秒(n = 18)。分别在暴露于乙酰胆碱30秒和5分钟后,从脱敏作用的快速相和慢速相恢复的时间常数分别为52秒和222秒。这表明脱敏作用涉及两个过程。4. 脱敏作用快速相速率常数的Q10为2.2±0.3(n = 6)。5. 用鸟苷5'-O-(3-硫代三磷酸)(GTPγS)进行细胞内灌注或用AlF4-进行细胞外灌注,以绕过毒蕈碱受体,并通过直接激活将毒蕈碱受体与钾通道相连的G蛋白GK来触发IK,ACh。GTPγS和AlF4-激活的电流与乙酰胆碱激活的电流具有相同的反转电位和相同程度的内向整流。6. 当毒蕈碱受体被绕过且通过GTPγS或AlF进行直接激活GK来触发IK,ACh时,仍然会发生脱敏作用。这表明脱敏作用部分是GK或钾通道修饰的结果。7. 乙酰胆碱对毒蕈碱受体的激活导致的脱敏作用比直接激活GK更明显;在暴露于乙酰胆碱5分钟结束时,电流仅为其峰值的22±1%(n = 19),而在通过GTPγS直接激活GK 5分钟后,电流为其峰值的42±6%(n = 5)。这表明脱敏作用也涉及毒蕈碱受体。8. 当细胞用GTPγS灌注时,仍然会出现脱敏作用的快速相,但慢速相减少。这表明快速相涉及GK或钾通道,而慢速相涉及毒蕈碱受体。(摘要截短于400字)

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