• 沒有找到結果。

Auchere, D., Tardivel, S., Gounelle, J.-C., Drueke,T. and Lacour, B.

Role of transcellular pathway in ileal Ca2+ absorption: stimulation by low-Ca2+ diet. Am J Physiol 275:G951-956, 1998.

Barrett KE. Positive and negative regulation of chloride secretion in T84 cells. Am J Physiol 265: C859-C868, 1993.

Berg RD, Garlington AW. Translocation of certain indigenous bacteria from the gastrointestinal tract to the mesenteric lymph nodes anf other organs in a gnotobiotic mouse model. Infect Immun 23:

403-11, 1979.

Binder HJ, Sandle GI. Electrolyte transport in the mammalian colon.

In Physiology of the Gastrointestinal Tract. LR Johnson (ed). New York, Raven Press. 1994, pp 2133-2172.

Chiossone DC, Simon PL, and Smith PL. Interleukin-1: Effect on rabbit ileal mucosal ion transport in vitro. Eur J Pharmacol.180:

217-228, 1990.

Christensen O, Bindslev N. Fluctuation analysis of short-circuit current in a warm-blooded sodium-retaining epithelium: site current, J Membr Biol 65: 19-30,

1982.

Class W, Durr JE, Guth D, Skadhauge E. Effects of adrenal steroids on Na transport in the lower intestine (coprodeum) of the hen. J Membr Biol 96: 141-52, 1987.

Field M, Fromm D, Al-Awqati Q, Greenough WB. Effect of cholera enterotoxin on ion transport across isolated ileal mucosa. J Clin Invest 51: 796-804, 1972.

Field M. Intestinal secretion. Gastroenterology 66: 1063-1084, 1974.

Fondacaro, J.D. Intestinal ion transport and diarrheal disease. Am J Physiol 250:G1-8, 1986.

Gabriel, S. E., S. E. Davenport, R. J. Steagall, V. Vimal, T. Carlson, and E. J. Rozhon. A novel plant-derived inhibitor of cAMP-mediated fluid and chloride secretion. Am J Physiol 276 (Gastrointest. Liver Physiol. 39): G58-G63, 1999.

Gall, D.G. Gastrointestinal uptake of macromolecule. Acta Paed Sin 39: 9-11, 1998.

Hansen MB, Bindslev N. Serotonin-induced chloride secretion in hen colon. Possible second messengers. Comp Biochem Physiol 94A:

315-21, 1989.

Hansen MB, Skadhauge E. New aspects of pathophysiology and treatment of secretory diarrhea. Physio Res 44: 61-78, 1995.

Hansen MB, Thorboll JE, Christensen P, Bindslev N, Skadhauge E.

Secretonin-induced short-circuit current in pig jejunum. J Vet Med A41: 110-20, 1994.

Holtug K, Shipley A, Dantzer V, Sten Knudsen O, Skadhauge E.

Localization of sodium absorption and chloride secretion in an intestinal epithelium. J Membr Biol 122: 215-29, 1991.

Holtug K, Skadhauge E. Ion transport across isolated pig jejunum.

Am J Physiol 260: G220-31, 1991.

Izzo, A.A., Mascolo, N. and Capasso, F. Nitric oxide as a modulator of intestinal water and electrolyte transport. Digest Dis and Sci 43:

1605-1620, 1998.

Jodal M, Holmgren S, Lundgren O, Sjoqvist A. Involvement of the myenteric plexus in the cholera toxin induced net fluid secretion in the rat small intestine. Gastroenterology 105: 1286-1293, 1993.

Kase, Y., Hayakawa, T, Takeda, S, Ishige, A., Aburada, M. and Okada, M Pharmacological studies on antidiarrheal effects of Hange-shashin-to. Biol & Pharmaceut Bull 19: 1367-70, 1996.

Kase, Y., Hayakawa, T, Takeda, S, Ishige, A., Aburada, M. and Okada, M Effects of Keishi-ka-shakuyaku-to (Gui-Zhi-Jia-Shao-Yao-Tang) on diarrhea and small intestinal movement. Biol & Pharmaceut Bull 22: 87-9, 1998.

Kiliaan, A.J., Saunders, P.R., Bijisma, P.B., Berin, M.C., Taminiau, J.A., Groot, J.A. and Perdue, M.H. Stress stimulates transrepithelial macromolecular uptake in rat jejunum. Am J Physiol 275:

G1037-1044, 1998.

Kimberg DV, Field M, Johnson J, Henderson A, Gershon E.

Stimulation of intestinal mucosal adenyl cyclase by cholera enterotoxin and prostaglandins. J Clin Invest 50: 1218-1230, 1971.

Kimm, M.H., Curtis, G.H., Hardin, J.A. and Gall, D.G. Transport of bovine serum albumin across rat jejunum: role of the enteric nervous system. Am J Phsiol 266: G186-G193, 1994.

Konturek, P.H. et al. Involvement of nitric oxide anprostaglandin in gastroprotection induced by bacterial lipopolysacharide. Scand J Gastroenterol 33: 691-700, 1998.

Kurkchubasche A.G., Cardona, M., Watkins, S.C., Smith S.D., Albanese, C.T., Simmons, R.L., Rowe, M.I. and Ford, H.R.

Transmucosal passage of bacteria across rat intestinal epithelium in the Ussing Chamber: effect of nutritional factors and bacterial virulence. Shock 9: 121-127, 1998.

Madsen KL, Lewis SA, Tavernini MM, Hibbard J, and Fedorak RN.

Interleukin 10 prevents cytokine-induced disruption of T84 monolayer barrier integrity and limits chioride secretion.

Gastroenterology 113: 151-159, 1997.

Madsen KL, Tavernini MM, Mosmann TR,and Fedorak RN.

Interleukin 10 modulates ion transport in rats small intestine.

Gastroenterology 111: 936-944, 1996.

McEwan GT, Schousboe B, Skadhauge E. Effect of antisecretory factor on Escherichia coli STs enterotoxin-induced alkalinisation of pig. Pflugers Arch 417: 174-9, 1990.

Nolan JP, Hare DK, McDevitt JJ, Ali MV. In vitro studies of intestinal endotoxin absorption. I. Kinetics of absorption in the isolated everted gut sac. Gastroenterology 72: 434-9, 1977.

Osborne MP, Haddon SJ, Spencer AJ, et al. An electron microscopic investigation of time related changes in the intestine of neonatal mice infected with murine rotavirus. J Pediatr Gastroenterol Nutr 7:

236-48, 1988.

Osman, N.E., Westrom, B. and Karlsson, B. Serosal but not mucosal endotoxin exposure increases intestinal permeability in vitro in the rat.

Scand J Gastroenterol 33: 1170-1174, 1998.

Petritsch W, Eherer AJ, Holzer-Petsche U, Hinterleitner TA, Beubler E, Krejs GJ. Effect of cholera toxin on the human jejunum. Gut 33:

1174-1178, 1992.

Powell DW, Binder HJ, Curran PF. Electrolyte secretion by the

guinea pig ileum in vitro. Am J Physiol 223: 531-537, 1972.

Powell, D.W. (1995) Approach to the patient with diarrhea. in Textbook of Gastrorenterology. ed. by T. Yamada et al. 2nd ed. J.B. Lippincott Company. pp813-863.

Pugin J, Schurer-Maly CC, Leturcq D, Moriarty A, Ulevitch RJ, Tobias PS. Lipopolysaccharide activation of human endothelial and epithelial cells is mediated by lipopolysaccharide-binding protein and soluble CD14. Proc Natl Acad Sci USA 90: 2744-8, 1993.

Rask-Madsen J, Bukhave K, Beubler E. Influence on intestinal secretion of eicosanoids. J Intern Med Suppl 732: 137-44, 1990.

Rask-Madsen J, Hjelt K. Effect of amiloride on electrical activity and electrolyte transport in human colon. Scand J Gastroenterol 12: 1-6, 1977.

Schirgi-Degen A. and Beubler E. Proabsorptive properties of nitric oxide. Digestion. 59: 400-403, 1998.

Sheldon RJ, Malachick ME, Fox DA, Burks TF, Porreca F.

Pharmacological characterization of neural mechanisms regulating mucosal ion transport in mouse. J Pharmacol Exp Ther 249: 572-582, 1989.

Starkey WG, Candy DCA, Thornber D, et al. An in vivo model to study aspects of the pathophysiology of murine rotravirus-induced diarrhea. J Pediatr Gastroenterol Nutr 10: 361-70, 1990.

Starkey WG, Candy DCA,Thornber D, et al. An in vitro model to study aspects of the pathophysiology of murine rotavirus-induced diarrhea. J Pediatr Gastroenterol Nutr 10: 361-70, 1990.

Tabcharani, J. A., W. Low, D. Elie, and J. W. Hanrahan.

Low-conductance chloride channel activated by cAMP in the

epithelial cell line T84. FEBS Lett. 270: 157-163, 1990.

Theodorou V, Eutamene H, Fioramonti J, Junien JL, and Bueno L.

Interleukin-1 induces a neurally mediated colonic secretion in rats:

Involvement of mast cells and prostaglandins. Gastroenterology 106:

1493-944, 1994.

Trezise, A. E. O., and M. Buchwald. In vivo cell-specific expression of the cystic fibrosis transmembrane conductance regulator. Nature 353: 434-437, 1991.

Ubillas, R., S. D. Jolad, R. C. Bruening, M. R. Kernan, S. R. King, D.

F. Sesin, M. Barrett, C. A. Stoddart, T. Flaster, J. Kuo, F. Ayala, E.

Meza, M. Castanel, D. MeMeekin, E. Rozhon, M. S. Tempesta, D.

Barnard, J. Huffman, D. Smee, R. Sidwell, K. Soike, A. Brazier, S.

Safrin, R. Orlando, P. T. Kenny, N. Berova, and K. Nakanishi.

SP-303, an antiviral oligomeric proanthocyanidin from the latex of Croton lechleri (Sangre de Drago).Phytomedicine 1: 77-106, 1994.

表一、中藥酒精萃取物冷凍乾燥後所得的重量及實驗刺激的濃度 酒精萃取物

乾燥前體 積(ml)

乾燥後

重量(g) 濃縮液(ul) 刺激量(mg) 實驗刺激的濃度 (mg/ml)

黃柏 5 0.0598 25 0.299 0.0299

黃連 5 0.0711 25 0.3555 0.03555

鴉膽子 5 0.1601 25 0.8005 0.08005

苦參 5 0.0082 25 0.041 0.0041

秦皮 5 0.0342 25 0.171 0.0171

大黃 5 0.0470 25 0.235 0.0235

巴豆 5 0.0174 25 0.087 0.0087

牽牛子 5 0.0638 25 0.319 0.0319

火麻仁 5 0.0256 25 0.128 0.0128

表二、中藥水萃取物冷凍乾燥後所得的重量及實驗刺激的濃度 水萃取物

乾燥前體 積(ml)

乾燥後

重量(g) 濃縮液(ul) 刺激量(mg) 實驗刺激的濃度 (mg/ml)

黃柏 5 0.0311 25 0.1555 0.01555

黃連 5 0.0269 25 0.1345 0.01345

鴉膽子 5 0.0202 25 0.0101 0.00101

苦參 5 0.0290 25 0.145 0.0145

秦皮 5 0.0334 25 0.167 0.0167

大黃 5 0.0184 25 0.092 0.0092

巴豆 5 0.0214 25 0.107 0.0107

牽牛子 5 0.0646 25 0.323 0.0323

火麻仁 5 0.0040 25 0.02 0.002

表三、離子成分分析 離子成分

Mg(mM) K(mM) Na(mM) Ca(mM)

黃柏 0.49 2.09 0.21 0.0525

黃連 0.84 2.82 0.34 0.085

鴉膽子 7.57 0.74 undectable undectable

苦參 4.23 1.91 0.61 0.1525

秦皮 5.42 1.66 0.04 0.01

大黃 5.57 0.15 undectable undectable

巴豆 2.35 1.87 0.09 0.0225

牽牛子 1.93 1.76 1.26 0.315

火麻仁 2.6 5.7 2.79 0.6975

表四、不同藥材酒精抽出物對於 Forskolin 刺激大白鼠腸道上皮組織 間離子電流的影響,數值單位為μA,括弧內為標準差。

藥材 樣本數 起始值 加 Forskolin 加抽出物 電流變化值

對照組 3 57.3 105.7 105.0 -0.7(1.5)

黃連 6 58.8 109.2 95.7 -13.5(8.4)

黃柏 6 47.3 103.2 96.2 -7.0(2.4)

鴉膽子 6 50.0 94.0 86.0 -8.0(3.0)

苦參 6 52.3 79.3 73.7 -5.6(1.7)

秦皮 6 35.3 88.5 80.0 -8.5(2.0)

大黃 6 45.2 95.5 109.8 +14.3(3.1)

巴豆 6 42.0 98.7 113.3 +14.6(3.0)

牽牛子 6 40.8 95.3 113.7 +18.4(4.1)

火麻仁 6 47.0 99.7 112.8 +13.1(2.9)

表五、不同藥材水抽出物對於 Forskolin 刺激大白鼠腸道上皮組織間 離子電流的影響,數值單位為μA,括弧內為標準差。

藥材 樣本數 起始值 加 Forskolin 加抽出物 電流變化值

對照組 3 57.3 105.7 105.0 -0.7(1.5)

黃連 3 62.4 109.2 107.2 -2(3.46)

黃柏 3 45.2 110.6 107.2 -3.4(1.15)

鴉膽子 3 53.8 121.4 119.0 -2.4(1.15)

苦參 3 56.8 110.3 105.9 -4.4(1.53)

秦皮 3 43.3 91.2 90.2 -1(1.0)

大黃 3 43.9 98.7 100.4 +1.7(0.57)

巴豆 3 54.3 113.6 120.3 +6.7(2.08)

牽牛子 3 48.4 110.4 113.0 +2.6(1.52)

火麻仁 3 54.1 109.5 112.2 +1.7(1.15)

圖一、forskolin 對於大白鼠腸道短路電流的影響。大白鼠腸道上皮在 架上 Ussing chamber 後,箝制上皮兩端電壓同時,可測得上皮間一短 路電流,此電流約在 40µA 左右,為上皮細胞進行正常離子主動運輸 所造成,在漿膜端加入 5µM forskolin,引發細胞內 cAMP 增加並導 致氯離子分泌增加,而使短路電流驟升至 70µA 上下,此上升之短路 電流通常可持續一兩個小時。

圖二、黃柏酒精抽出物對於接受 forskolin 刺激大白腸道上皮短路電流 的影響。接受 forskolin 刺激大白鼠腸道上皮,在加入黃柏酒精抽出物 後,短路電流明顯下降。

圖三、秦皮酒精抽出物對於接受 forskolin 刺激大白腸道上皮短路電流 的影響。接受 forskolin 刺激大白鼠腸道上皮,在加入秦皮酒精抽出物 後,短路電流明顯下降。

圖四、巴豆酒精抽出物對於接受 forskolin 刺激大白腸道上皮短路電流 的影響。接受 forskolin 刺激大白鼠腸道上皮,在加入巴豆酒精抽出物 後,短路電流明顯上升。

圖五、大黃酒精抽出物對於接受 forskolin 刺激大白腸道上皮短路電流 的影響。接受 forskolin 刺激大白鼠腸道上皮,在加入大黃酒精抽出物 後,短路電流明顯上升。

圖六、不同藥材酒精抽出物對於 forskolin 刺激大白鼠腸道上皮離子電 流的影響,括弧內為樣本數。具止瀉功能之中草藥黃連、鴉膽子、秦 皮、苦參、黃柏酒精抽出濃縮物質均則可使接受 forskolin 刺激之大白 鼠腸道上皮短路電流下降。具瀉下功能之中草藥酒精抽出濃縮物質則 可使接受 forskolin 刺激之大白鼠腸道上皮短路電流上升。

圖七、鈉離子與氯離子移動與秦皮酒精抽出物影響腸道上皮短路電流 之關係。接受 forskolin 刺激大白鼠腸道上皮之短路電流之後分別給予 ouabain 及 bumetanide 處理,再加入秦皮酒精抽出物,腸道上皮短路 電流變化值。以 ouabain 處理,再加秦皮酒精抽出物,短路電流變化 值與對照組差異不甚明顯,以 bumetanide 處理,再加秦皮酒精抽出 物,短路電流變化值對照組則有明顯差異。(n=6),*p<0.05 v.s control。

圖八、鈉離子與氯離子移動與黃連酒精抽出物影響腸道上皮短路電流 之關係。以 ouabain 處理,再加黃連酒精抽出物,短路電流變化值為 與對照組差異不甚明顯(p=0.187)(n=6)。以 bumetanide 處理,再加 黃連酒精抽出物,短路電流變化值也與對照組(p=0.09)差異不明顯。

(n=6)。

圖九、鈉離子與氯離子移動與苦參酒精抽出物影響腸道上皮短路電流 之關係。以 ouabain 處理,再加苦參酒精抽出物,短路電流變化值對 照組有明顯差異。以 bumetanide 處理,再加苦參酒精抽出物,短路電 流變化值與對照組差異不甚明顯(n=6)。*p<0.05 v.s control。

圖十、鈉離子與氯離子移動與大黃酒精抽出物影響腸道上皮短路電流 之關係。以 ouabain 處理,再加大黃酒精抽出物,短路電流變化值與 對照組(14.33 ±3.07µA)差異明顯。以 bumetanide 處理,再加大黃 酒精抽出物,短路電流變化值與對照組也有明顯差異。(n=6),*p<

0.05 v.s control。

圖十一、鈉離子與氯離子移動與巴豆酒精抽出物影響腸道上皮短路電 流之關係。以 ouabain 處理,再加巴豆酒精抽出物,短路電流變化值 與對照組差異明顯。以 bumetanide 處理,再加巴豆酒精抽出物,短路 電流變化值與對照組也有明顯差異。(n=6),*p<0.05 v.s control。

圖十二、鈉離子與氯離子移動與火麻仁酒精抽出物影響腸道上皮短路 電流之關係。以 ouabain 處理,再加火麻仁酒精抽出物,短路電流變 化值與對照組)差異明顯(p=0.003)。以 bumetanide 處理,再加火麻 仁酒精抽出物,短路電流變化值,與對照組也有明顯差異。(n=6),

*p<0.05 v.s control。

圖十三、苦參酒精抽出物對鈉離子移動的影響。接受 forskolin 刺激大 白鼠腸道上皮,給予苦參酒精抽出物,結果顯示在加入苦參之後,短 路電流明顯下降,再以 ouabain 處理,短路電流變化值再度下降,平 均下降值與對照組(接受 forskolin 刺激之後給予 ouabain) 電流平均值 下降值差異明顯。(n=4),*p<0.05 v.s control。

圖十四、秦皮酒精抽出物對氯離子移動的影響

接受 forskolin 刺激 大白鼠腸道上皮,給予秦皮酒精抽出物,結果顯示在加入秦皮之後,

短路電流明顯下降,再以 bumetanide 處理之後,短路電流變化值再度 下降,與對照組(接受 forskolin 刺激之後給予 bumetanide) 電流平均 下降值差異明顯。(n=4),*p<0.05 v.s control。

相關文件