Responsive image
博碩士論文 etd-0530104-222719 詳細資訊
Title page for etd-0530104-222719
論文名稱
Title
澤瀉萃取物對青蛙皮膜組織短路電流及通透性的影響
Effects of Alismatis Rhizoma's Extract on Short – Circuit Current and Conductance across Frog Skin Epithelium
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
49
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
2004-03-16
繳交日期
Date of Submission
2004-05-30
關鍵字
Keywords
澤瀉
Alismatis rhizoma, voltage-clamp, short-circuit current
統計
Statistics
本論文已被瀏覽 5735 次,被下載 3066
The thesis/dissertation has been browsed 5735 times, has been downloaded 3066 times.
中文摘要
在中藥運用上,澤瀉 ( Alismatis rhizoma ) 屬利水滲濕藥,主要用途為利尿、治療水腫和抗發炎,其作用機轉未見諸文獻報告。利尿作用通常與泌尿系統上皮細胞對鈉離子的重吸收有關,因此推測澤瀉也許能影響皮膜細胞對鹽類及水分通透的作用,本研究之目的即試圖透過短路電流 ( short – circuit current,Isc ) 之測定,檢測上述假設推論是否成立。由於皮膜兩側鈉離子濃度的變化,會導致短路電流改變。本實驗以電壓箝制技術 ( voltage – clamp technique ),探討澤瀉萃取物 ( extracts of Alismatis rhizoma,ARE ) 作用於青蛙腹部皮膜後,對其短路電流 ( Isc ) 及鈉離子通透性的影響。在穩定狀態時,皮膜電位差為64.81 ± 2.44 mV,Isc為59.82 ± 3.58 μA / cm2 ,電導值 ( G ) 為1.09 ± 0.18 μA / cm2 / mV 。在黏膜側加入ARE會使Isc下降約24%,若作用於漿膜側則Isc約降低10%,但兩者電導值都沒有明顯改變。以ARE作用於黏膜側使Isc降低,至達到穩定狀態後,再加入鈉離子通道阻斷劑amiloride,會使Isc進一步下降。反之,若先以amiloride處理黏膜側,再加入ARE則無法使Isc繼續降低。
以一氧化氮 ( nitric oxide,NO ) 的前驅物L-arginine,作用於漿膜側可使Isc增加17.10 ± 9.30 μA/cm2,而能夠直接釋放NO的S-nitroso-N-acetyl-penicillamine ( SNAP ) 卻無法影響Isc。若漿膜側先以ARE或NO synthase抑制劑NG-L-nitro-arginine methyl ester ( L-NAME ) 處理,則可抑制L-arginine造成的Isc升高現象 。
由以上結果顯示,澤瀉在皮膜兩側均可產生作用。在黏膜側使Isc降低的程度,較作用於漿膜側顯著,而澤瀉在黏膜側的作用機制可能與amiloride – sensitive sodium channel有關。至於澤瀉在漿膜側的部分作用,則可能與抑制NO的生成或NO的訊息傳遞路徑有關,間接影響受NO所調控的離子運輸作用。
Abstract
In traditional Chinese herb medicine, Alismatis rhizoma has been used in treating edema, inflammation and increasing urine flow. Mechanism of Alismatis rhizoma’s effect on these functions has not been elucidated. Since diuresis has been considered closely related to the reabsorption of sodium ion via the epithelium of tubule and collecting duct in kidney, we suspected that Alismatis rhizoma may influence transportation of salt and water.
The measurement of short circuit current ( Isc ) has been used widely to estimate the ion transportation between mucosal and serosal side of epithelium. In the present experiment, we used the voltage – clamp technique to demonstrate the effect of Alismatis rhizoma’s extracts ( ARE ) on Isc and sodium ion conductance in frog skin. Our result showed that in control stage, the potential difference ( PD ) of frog skin is 64.81 ± 2.44 mV, the Isc is 59.82 ± 3.58 μA / cm2 and the conductance is 1.09 ± 0.18 μA / cm2 / mV.
After ARE was applied to mucosal side of the frog skin, its Isc decrease from 62.63 ± 5.31 μA / cm2 to 47.92 ± 5.41 μA / cm2, which could further go down to 3.36 ± 1.06 μA/cm2 by adding amiloride. Treating serosal side of frog skin with ARE decreased approximately 10% of its Isc. No apparent changes in conductance were observed by adding ARE to mucosal ( 0.98 ± 0.24 μA / cm2 / mV ) or serosal side ( 0.96 ± 0.23 μA / cm2 / mV ).
Adding L-arginine ( the precursor of nitric oxide ) to the serosal side of the skin epithelium elevated the Isc for 17.10 ± 9.30 μA/cm2. This effect can be inhibited by applying ARE or NG-L-nitro-arginine methyl ester ( L-NAME, NO synthase inhibitor ) before application of L-arginine.
In summary, Alismatis rhizoma could affect Isc on both mucosal and serosal sides of the frog skin. Its effect on lowering Isc was more obvious when applied to the mucosal side than to the serosal side. The ARE may exert its effect on mucosal side by affecting amiloride–sensitive sodium channel and on serosal side by affecting the NO signal transduction pathway.
目次 Table of Contents
目 錄
頁次
目錄-----------------------------------------I
圖表目錄------------------------------------Ⅱ
中文摘要-------------------------------------1
英文摘要-------------------------------------2
文獻回顧及研究目標---------------------------4
實驗材料及方法------------------------------12
結果----------------------------------------18
討論----------------------------------------21
結論----------------------------------------27
參考文獻------------------------------------28

圖表目錄
頁次
表一. 本實驗各種藥物對皮膜作用後的短路電流 ( Isc )、電
導值 ( G ) 以及短路電流變化百分比( DIsc )列表--33
圖一. 澤瀉部分組成份之化學結構--------------------34
圖二. KJU 模型及電壓箝制 ( voltage – clamp ) 示意圖---35
圖三. 澤瀉作用於黏膜側及漿膜側對短路電流的影響----36
圖四. Amiloride 與澤瀉的配對作用-------------------37
圖五. L-Arginine 作用在漿膜側以及黏膜側對短路電流的影
響----------------------------------------38
圖六. 澤瀉與L-NAME對L-arginine 造成Isc 升高的抑制作用
-----------------------------------------39
圖七. SNAP 作用於漿膜側對短路電流的影響----------40
圖八. 漿膜側的鹼性環境對短路電流的影響------------40
圖九. 澤瀉及Amiloride 在黏膜側個別作用和配對作用時,對
短路電流影響之統計圖------------------------41
圖十. 澤瀉作用於漿膜側對於短路電流影響統計圖------42
圖十一.L-Arginine、SNAP 以及KOH 作用於漿膜側對短路
電流影響統計圖---------------------------43
圖十二.L-NAME 以及澤瀉在漿膜側抑制L-arginine 作用之統
計圖---------------------------------------44
圖十三.體積濃度2%之酒精溶液對皮膜短路電流的影響--45
圖十四.酒精濃度序列增加對黏膜側短路電流的影響-----46
圖十五.黏膜側的酸性環境對短路電流的影響-----------46
參考文獻 References
參考文獻

蕭培根, 連文琰 ( 1998 ) 原色中藥原植物圖鑑, pp. 517. 南天書局, 台北.

陳榮福 ( 1991 ) 中藥藥理學, pp. 195 – 198. 國立中國醫藥研究所.

林宗旦, 林宗平, 林景彬 ( 1996 ) 中藥藥理學, pp. 228 – 230. 國立編譯館, 台北.

Canessa, C. M., Merillat, A. M., and Rossier, B. C. ( 1994 ) Membrane topology of the epithelial sodium channel in intact cells. Am. J. Physiol. 267 ( 6 Pt 1 ) : C1682 – 1690.

Chalfant, M. L., Denton, J. S., and Berdiev, B. K. ( 1999 ) Intracellular H+ regulates the alpha-subunit of ENaC, the epithelial Na+ channel. Am. J. Physiol. 276 ( 2 Pt 1 ) : C477 – 486.

Courtois-Coutry, N., Le Moellic, C., and Boulkroun S. ( 2002 ) Calcyclin is an early vasopressin-induced gene in the renal collecting duct. Role in the long term regulation of ion transport. J. Biol. Chem. 277 ( 28 ) : 25728 – 25734.

Ding, J. W., Dickie, J., and O’Brodovich, H. ( 1998 ) Inhibition of amiloride-sensitive sodium channel activity in distal lung epithelial cells by nitric oxide. Am. J. Physiol. 274 ( 3 Pt 1 ) : L378 – 387.

Eaton, D. C., Malik, B., and Saxena, N. C. ( 2001 ) Mechanisms of aldosterone’s action on epithelial Na+ transport. J. Membrane Biol. 184 : 313 – 319.

Ester, W. A., Coen, A. S., and Peter, H. ( 2003 ) Protective role of endothelial nitric oxide synthase. J. Pathol. 199 : 8 – 17.

Fushmi, K., Uchida, S., and Hara, Y. ( 1993 ) Cloning and expression of apical membrane water channel of rat kidney. Nature 361 ( 6412 ) : 549 – 552.

Gabel, G., Garz, B., and Ahrens, F. ( 2003 ) Effect of nitric oxide on electrolyte transport across the porcine proximal colon. J. Comp. Physiol. 173 ( 3 ) : 177 – 186.

Galietta, L. J., Musante, L., and Romio, L. ( 1998 ) An electrogenic amino acid transporter in the apical membrane of cultured human bronchial epithelial. Am. J. Physiol. 275 ( 5 Pt 1 ) : L917 – 923.

Hamilton, K. L., Eaton, D. C. ( 1985 ) Single–channel recordings from amiloride-sensitive epithelial sodium channel. Am. J. Physiol. 249 ( 3 Pt 1 ) : C200 – 207.

Harvey, B. J., Thomas, S. R. and Ehrenfeld, J. ( 1988 ) Intracellular pH controls cell membrane Na+ and K+ conductances and transport in frog skin epithelium. J. Gen. Physiol. 92 ( 6 ) : 767 – 791.

Homaidan, F. R., Martello, L. A., and Melson, S. J., ( 1998 ) Regulation of electrolyte transport by nitric oxide in the mouse cecum. Eur. J. Pharmacol. 350 ( 1 ) : 93 – 99.

Howard, D. P. J., Cuffe, J. E. and Boyd, C. A. R., ( 2001 ) L-Arginine effects on Na+ transport in M-1 mouse cortical collecting duct cells – a cationic amino acid absorbing epithelium. J. Membrane Biol. 180 : 111 – 121.

Kim, N. Y., Kang, T. H. and Pae, H. O. ( 1999 ) In vitro inducible nitric oxide synthesis inhibitors from Alismatis Rhizoma. Biol. Pharm. Bull. 22 ( 10 ) : 1147 – 1149.

Koefoed – Johnsen, V., Ussing, H. H. ( 1958 ) The nature of the frog skin potential. Acta Physiol. Scand. 42 : 298 – 308.

Kone, B. C. ( 1997 ) Nitric oxide in renal health and disease. Am. J. Kidney Dis. 30 ( 3 ) : 311-33.

Lindemann, B. ( 2001 ) Hans Ussing, Experiments and models. J. Membrane Biol. 184 : 203 – 210.

Lindemann, B., van Driessche, W. ( 1977 ) Sodium-specific membrane channels of frog skin are pores : current fluctuations reveal high turnover. Science 195 ( 4275 ) : 292 – 294.

Li, Y. F., Weisbrodt, N. W., and Lodato, R. F. ( 1994 ) Nitric oxide is involved in muscle relaxation but not in changes in short-circuit current in rat ileum. Am. J. Physiol. 266 ( 4 Pt 1 ) : G554 – 559.

Louis, J. I., Claudio, N., and Joseph L. ( 2002 ) Nitric oxide donors and cardiovascular agents modulating the bioactivity of nitric oxide – an overview. Circ. Res. 90 : 21 – 28.

MacNaughton, W. K., Lowe, S. S., and Cushing, K. ( 1998 ) Role of nitric oxide in inflammation – induced suppression of secretion in a mouse model of acute colitis. Am. J. Physiol. 275 ( 6 Pt 1 ) : G1353 – 1360.

Michinori, K., Hideaki, M., and Norimichi, T. ( 1997 ) Studies on Alismatis Rhizome. I. anti – allergic effects of methanol extract and six terpene components from Alismatis Rhizoma ( dried rhizome of Alisma orientale ) . Biol. Pharm. Bull. 20 ( 5 ) : 511 – 516.

Neumann, V., Norris, B., and Concha, J. ( 1996 ) Influence of nitric oxide on transepithelial transport in toad skin : effects of cholinergic agents and morphine. Eur. J. Pharmacol. 316 ( 1 ) : 123 – 128.

Palmer, L. G. ( 1987 ) Ion selectivity of epithelial Na channels. J. Membrane Biol. 96 : 97 – 106.

Palmer, L. G. and Frindt, G. ( 1987 ) Effects of cell Ca and pH on Na channels from rat cortical collecting tubule. Am. J. Physiol. 253 ( 2 Pt 2 ) : F333 – 339.

Palmer, L. G. ( 2001 ) Intracellular pH as a regulator of Na+ transport. J. Membrane Biol. 184 : 305 – 311 .

Pascal, B., Michel, L. ( 1996 ) Structure and regulation of the amiloride-sensitive epithelial sodium channel. In : Ion channels, Vol. 4, edited by Toshio, N. pp. 115 – 167.

Reuss, L. ( 2001 ) Ussing’s two–membrane hypothesis : the model and half a century of progress. J. Membrane Biol. 184 : 211 – 217.

Tsai, L. H., Chou, L. S., and Liu, H. J. ( 1988 ) The mechanism of diuretic action of Alismatis Rhizoma crude extract. 北醫學報 ( 17 ) : 31 – 39.

Zai, A., Rudd, M. A. and Scribner, A. W. ( 1999 ) Cell-surface protein disulfide isomerase catalyzes transnitrosation and regulates intracellular transfer of nitric oxide. J. Clin. Invest. 103 ( 3 ) : 393-399.
電子全文 Fulltext
本電子全文僅授權使用者為學術研究之目的,進行個人非營利性質之檢索、閱讀、列印。請遵守中華民國著作權法之相關規定,切勿任意重製、散佈、改作、轉貼、播送,以免觸法。
論文使用權限 Thesis access permission:校內外都一年後公開 withheld
開放時間 Available:
校內 Campus: 已公開 available
校外 Off-campus: 已公開 available


紙本論文 Printed copies
紙本論文的公開資訊在102學年度以後相對較為完整。如果需要查詢101學年度以前的紙本論文公開資訊,請聯繫圖資處紙本論文服務櫃台。如有不便之處敬請見諒。
開放時間 available 已公開 available

QR Code