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博碩士論文 etd-0620102-192529 詳細資訊
Title page for etd-0620102-192529
論文名稱
Title
腦垂腺GH3細胞受動作電位波形誘發出L型鈣離子電流之研究
Properties of Action Potential Waveform-Evoked L-type Calcium Currents in Pituitary GH3 Cells
系所名稱
Department
畢業學年期
Year, semester
語文別
Language
學位類別
Degree
頁數
Number of pages
42
研究生
Author
指導教授
Advisor
召集委員
Convenor
口試委員
Advisory Committee
口試日期
Date of Exam
2002-06-06
繳交日期
Date of Submission
2002-06-20
關鍵字
Keywords
L 型鈣離子流、動作電位、泌乳激素、腦垂腺、鈣離子
ACTION POTENTIAL, GH3, PATCH CLAMP, TRH
統計
Statistics
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The thesis/dissertation has been browsed 5679 times, has been downloaded 3916 times.
中文摘要
GH3 細胞是A.H. Tashjian Jr.等人於1965年由老鼠腦垂腺前葉腫瘤衍生出來的一種神經內分泌細胞,它可以自發性地分泌泌乳激素 (prolactin),其機制可能與鈣離子依賴性動作電位(Ca2+-dependent action potentials)有關。本實驗的目的是利用whole-cell patch-clamp 方法,檢測GH3細胞在不同波形的動作電位作用之下所產生的L型鈣離子流(L-type Ca2+ current or ICa,L) 的反應。實驗所得結果分述如下:
1. 動作電位誘發出來的ICa,L包含兩個部份,第一部份的波峰在動作電位上升段出現,第二部份的波峰在動作電位的下降段出現。
2. 延長動作電位下降段的時間,發現經由ICa,L進入的鈣離子流量增加,但其第二部份波峰的高度下降。
3. 動作電位停留於波峰的時間增長, ICa,L第二部份的波峰隨之增高。
4. 以一連串的動作電位刺激時,導致 ICa,L有不活化的現象。以Ba2+取代溶液中的帶電電荷時,ICa,L的不活化現象明顯減少。
5. 以不規則的爆發性動作電位激發出來的ICa,L有不活化的現象。
6. 以一連串達到去極化電位的動作電位持續刺激細胞時,鈣離子不只在動作電位發生的過程中進入細胞,在兩個連續動作電位的間隔時間裡,鈣離子也能進入細胞。
7. 以方形波刺激時,加入thyrotropin releasing hormone (TRH; 10 µM)所測得的ICa,L比加入前所測得的值大,且其電流與電壓的關係圖略向負方移動。
8. 當細胞浸浴於TRH (10 µM),thapsigargin (10 µM),或是cyclopiazonic acid (30 µM),以動作電位誘發出ICa,L時,第二波峰的強度會增強。
9. 連串地動作電位刺激使ICa,L不活化的現象,在加入TRH後大為減少。
10. 細胞內儲存的鈣離子是否釋放出來,是影響動作電位誘發的ICa,L強度的因素之一。
以上結果顯示,在腦垂腺GH3細胞上以動作電位波形誘發出的ICa,L,其time course以及動力學的表現,與我們以方形波刺激所得到的數據完全不同。改變GH3細胞動作電位的波形以及其激發的形態,可以調節經由L型鈣離子通道進入的鈣離子流量。


Abstract
The purpose of this study was to examine the time course and kinetics of L-type Ca2+ current (ICa,L) from pituitary GH3 cells in response to various action potential (AP) waveforms using the whole-cell configuration of the patch-clamp technique. The major findings in this study are:
1. ICa,L evoked during the AP waveform exhibited an early and a late component. The early component of ICa,L occurred on the rising phase of the AP, whereas the late component coincided with the falling phase.
2. A prolongation of the falling phase of APs led to an increase in Ca2+ charge carried by ICa,L, although the amplitude of the late ICa,L was reduced.
3. When the peak voltage of AP waveforms was prolonged without changing the rising and falling phases, the amplitude of the late components was significantly increased.
4. ICa,L was also found to inactivate during a train of AP waveforms. When Ba2+ ions were used as the charge carriers, current inactivation during a train of APs was decreased.
5. The amplitude of ICa,L evoked by the AP templates with irregular bursting pattern was inactivated.
6. When spontaneous APs with the depolarizing potentials were replayed to GH3 cells, Ca2+ entry was not only spread over the entire AP, but also occurred during the interspike voltage trajectory.
7. When cells were exposed to thyrotropin releasing hormone (TRH; 10
目次 Table of Contents
前言......................1
關於patch clamp................1
關於GH3 細胞..................2
細胞對鈣離子的調控...............4
實驗目的....................5
研究方法與材料.................6
細胞培養....................6
電生理.....................6
資料記錄分析..................7
檢驗GH3 細胞L-type Ca2+ current (ICa,L) 的方法.7
動作電位波形的建立...............8
藥物與溶液製備.................9
結果.....................11
方形波與動作電位波形所誘發出來的ICa,L之比較.11
改變動作電位的波形對於ICa,L的影響......12
連續施以動作電位造成鈣離子通道的不活化....13
以達到去極化電壓的自發性動作電位誘發ICa,L..14
比較TRH對方形波與動作電位波形所引發的ICa,L的影響.15
延長動作電位下降段時間所激發出來的ICa,L對TRH的反應. .16
連串的動作電位波形所造成的不活化現象因TRH 而減少..16
細胞內鈣離子儲存量對動作電位誘發的ICa,L之影響..17
討論.....................18
參考文獻...................25
附圖.....................31
圖1.方型波所誘發出的ICa,L,其電流與電壓之相互關係.31
圖2.GH3 細胞受單一動作電位所誘發出的ICa,L....32
圖3.動作電位下降段時間延長對於ICa,L波形的影響....33
圖4.持續時間不同的波峰電壓對於動作電位誘發之ICa,L的影響..34
圖5.以一連串的動作電位刺激細胞所造成的ICa,L的不活化現象..35
圖6.自發性規則與不規則爆發性動作電位對ICa,L的影響....36
圖7.模擬細胞受TRH刺激後產生自發性連續動作電位對ICa,L的影響.37
圖8.TRH 對於方形波或是動作電位波形所誘發出的ICa,L的影響...38
圖9.TRH對延長動作電位的下降段之後誘發出的ICa,L的影響....39
圖10.連續施以動作電位所造成的ICa,L不活化現象受TRH影響而減少40
圖11.TRH , thapsigargin, cyclopiazonic acid 和 dantrolene 對於動作電位誘發出ICa,L的第二部份鈣離子總流量的影響之比較...41
表1.下降段持續時間長度不同的動作電位波形對於GH3 細胞ICa,L的第二部份之影響...........42
參考文獻 References
Barros F, Delgado LM, Maciá C, Peña P de la (1991) Effects of hypothalamic peptides on electrical activity and membrane currents of ‘patch perforated’ clamped GH3 anterior pituitary cells. FEBS Lett 279:33-37.
Barry WH, Bridge JHB (1993) Intracellular calcium homeostasis in cardiac myocytes. Circulation 87:1806-1815.
Bouchard RA, Clark RB, Giles WR (1995) Effects of action potential duration on excitation-contraction coupling in rat ventricular myocytes. Action potential voltage-clamp measurement. Circ Res 76:790-801.
Cleeman L, Morad M (1991) Role of Ca2+ channel in cardiac excitation-contraction coupling in the rat: evidence from Ca2+ transients and contraction. J Physiol(Lond)432:283-312.
Fabiato A (1985) Time and calcium dependence of activation and inactivation of calcium induced release of calcium from the sarcoplasmic reticulum of a skinned canine cardiac Purkinje cell. J Gen Physiol 85:247-289.
Gollasch M, Haller H, Schultz G, Hescheler J (1991) Thyrotropin-releasing hormone induces opposite effects on Ca2+ channel currents in pituitary cells by two pathways. Proc Natl Acad Sci 88:10262-10266.
Hamill OP, Marty A, Neher E, Sakmann B, Sigworth FJ (1981) Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches. Pflügers Arch 391:85-100.
Haug T, Sand O (1997) BK channels in intact clonal rat pituitary cells are activated by physiological elevations of the cytosolic Ca2+ concentration at the normal resting potential. Acta Physiol Scand 161:227-237.
Herrington J, Lingle CJ (1992) Kinetic and pharmacologic properties of low voltage Ca2+ current in rat clonal (GH3) pituitary cells. J Neurophysiol 68:213-232.
Hoth M, Penner R (1992) Depletion of intracellular calcium stores activates a calcium current in mast cells. Nature 355:353-356.
Hsu S-F, Augustine GJ, Jackson MB (1996) Adaptation of Ca2+-triggered exocytosis in presynaptic terminals. Neuron 17:501-512.
Iijima T, Sand O, Sekiguichi T, Matsumoto G (1990) Simultaneous recordings of cytosolic Ca2+ level and membrane potential and current during the response to thyroliberin in clonal rat anterior pituitary cells. Acta Physiol Scand 140:269-278.
Kalman D, O’Lague PH, Erxleben C, Armstrong DL (1988) Calcium-dependent inactivation of the dihydropyridine-sensitive calcium channels in GH3 cells. J Gen Physiol 92:531-548.
Lamberts SW, Macleod RM (1990) Regulation of prolactin secretion at the level of the lactotroph. Physiol Rev 70:279-318.
Llinas R, Sugimori M, Simon SM (1982) Transmission by presynaptic spike-like depolarization in the squid giant synapse. Proc Natl Acad Sci USA 79:2415~2419
Marrion NV, Tavalin SJ (1998) Selective activation of Ca2+-activated K+ channels by co-localized Ca2+ channels in hippocampal neurons. Nature 395:900-905.
McCobb DP, Beam KG (1991) Action potential waveform voltage-clamp commands reveal striking differences in Ca entry via low and high voltage-activated calcium channels. Neuron 7:119-127.
Mollard P, Theler JM, Gurineau N, Vacher P, Chiavaroli C, Schlegel W (1994) Cytosolic Ca2+ of excitable pituitary cells at resting potentials is controlled by steady state Ca2+ currents sensitive to dihydropyridines. J Biol Chem 269: 25158-25164.
Negretti N, O'Neill SC, Eisner DA (1993) The relative contribution of different intracellular and sarcolemmal systems to relaxation in rat ventricular myocytes. Cardiovasc Res 27:1826-1830.
Patil PG, Brody DL, Yue DT (1998) Preferential closed-state inactivation of neuronal calcium channels. Neuron 20:1027-1038.
Sabatini B, Regehr WG (1997) Control of neurotransmitter release by presynaptic waveform at the granule cell to Purkinje cell synapse. J Neurosci 17:3425-3435.
Sankaranarayanan S, Simasko SM (1996) Characterization of an M-like current modulated by thyrotropin-releasing hormone in normal rat lactotrophs. J Neurosci 16:1668-1678.
Scherübl H, Hescheler J (1992) Steady-state Ca2+ influx and electrical activity in endocrine cells. Trends Neurosci 15:126-127.
Schlegel W, Winiger BP, Mollard P, Vacher P, Wuarin F, Zahnd GR, Wollheim CB, Dufy B (1987) Oscillations of cytosolic Ca2+ in pituitary cells due to action potentials. Nature 329:719-721.
Scroggs RS, Fox AP (1992) Multiple Ca2+ currents elicited by action potential waveforms in acutely isolated adult rat dorsal root ganglion neurons. J Neurosci 12:1789-1801.
Simasko SM, Sankaranarayanan S (1997) Characterization of a hyperpolarization-activated cation current in rat pituitary cells. Am J Physiol 272:E405-E414.
Simasko SM, Weiland GA, Oswald RE (1988) Pharmacological characterization of two calcium currents in GH3 cells. Am J Physiol 254:E328-E336.
Stojilkovic SS, Izumi S-I, Catt KJ (1988) Participation of voltage-sensitive calcium channels in pituitary hormonal release. J Biol Chem 263:13054-13061.
Toth PT, Miller RJ (1995) Calcium and sodium currents evoked by action potential waveforms in rat sympathetic neurones. J Physiol 485:43-57.
Van Goor F, LeBeau AP, Krsmanovic L,Sherman A, Catt KJ, Stojilkovic SS(2000) Amplitude-dependent spike-broadening and enhanced Ca2+ signaling in GnRH-secreting neurons. Biophys J 79:1310~1323
Varro A, Negretti N, Hester SB, Eisner AD (1993) An estimate of the calcium content of the sarcoplasmic reticulum in rat ventricular myocytes. Pflugers Arch 423:158-160.
Wang X, Inukai T, Greer M, Greer S (1994) Evidence that Ca2+-activated K+ channels participate in the regulation of pituitary prolactin secretion. Brain Res 662:83-87.
Wier WG (1990) Dynamics of control of cytosolic calcium ion concentration. Annu Rev Physiol 52:467-485.
Willmott NJ, Asselin J, Galione A (1996) Calcium store depletion potentiates a phosphodiesterase inhibitor- and dibutyryl cGMP-evoked calcium influx in rat pituitary GH3 cells. FEBS Lett 386:39-42.
Wu SN, Li HF (1999) Characterization of riluzole-induced stimulation of large-conductance calcium-activated potassium channels in rat pituitary GH3 cells. J Investig Med 47:484-495.
Wu SN, Li HF, Jan CR (1998a) Regulation of Ca2+-activated nonselective cationic currents in rat pituitary GH3 cells: involvement in L-type Ca2+ current. Brain Res 812:133-141
Wu SN, Li HF, Jan CR, Chen IJ, Lo YC (1998b) Selective block by glyceryl nonivamide of inwardly rectifying K+ current in rat anterior pituitary GH3 cells. Life Sci 63:PL281-PL288.
Wu SN, Li HF, Jan CR, Shen AY (1999) Inhibition of Ca2+-activated K+ current by clotrimazole in rat anterior GH3 cells. Neuropharmacology 38:979-989.
Wu SN, Li HF, Chiang HT (2000) Actions of epoxyeicosatrienoic acid on large-conductance Ca2+-activated K+ channels in pituitary GH3 cells. Biochem Pharmacol 60:251-262.
Zuhlke RD, Pitt GS, Tsien RW, Reuter H (2000) Ca2+-sensitive inactivation and facilitation of L-type Ca2+ channels both depend on specific amino acid residues in a consensus calmodulin-binding motif in the α1C subunit. J Biol Chem 275:21121-22229.

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