참고문헌
- Colourful Clinical Materia Medica Shin, M.K.
- Native Herb (Crude Drug) Encyclopedia [a book of Plants] Chung, B.S.;Shin, M.K.
- Chem. Pharm. Bull. v.36 no.2 Studies on choleretic constituent in Artemisia capillaris THUNB. Okuno, I.;Uchida, K.;Nakamura, M.;Sakurawi, K. https://doi.org/10.1016/0006-2952(87)90733-7
- Planta Med. v.49 Mechanism of the hypotensive effect of scopoletin isolated from the fruit of Tetrapleura tetraptera. Ojewole, J. A. O.;Adesina, S. K. https://doi.org/10.1055/s-2007-969809
- Planta Med. v.49 Cardiovascular and neuromuscular action of scopoletin from the fruit of Tetrapleura tetraptera. Ojewole, J. A. O.;Adesina, S. K. https://doi.org/10.1055/s-2007-969824
- Eur. J. Biochem. v.233 Transient and steady-state kinetics of the oxidation of scopoletin by horseradish peroxidase compounds Ⅰ, Ⅱ and Ⅲ in the presence of NADH. Marquez, L. A.;Dunford, H. B. https://doi.org/10.1111/j.1432-1033.1995.364_1.x
-
Arch. Biocem. Biophys.
v.359
no.1
Ca
$^{2+}$ -stimulated mitochondrial reactive oxygen species generation and permeability transition are inhibited by dibucaine or Mg$^{2+}$ . Kowaltowski, A. J.;Naia-da-silva, E. S.;Castilho, R. F.;Vercesi, A. E. https://doi.org/10.1006/abbi.1998.0870 - Anal. Biochem. v.253 A stable nonfluorescent derivative of resorufin for the fluorometric determination of trace hydrogen peroxide: Applications in detecting the activity of phagocyte NADPH oxidase and other oxidases. Zhou, M.;Diwu, Z.;Voloshina, N. V.;Haugland, R. P. https://doi.org/10.1006/abio.1997.2391
-
Eur. J. Biochem.
v.148
NADPH oxidation catalyzed by the peroxidase/
$H_{2}O_{2}$ system: Guaiacol-mediated and scopoletin-mediated oxidation of NADPH to NADP+. Michot, J. L.;Virion, A.;Deme, D.;De Prailaune, S.;Pommier, J. https://doi.org/10.1111/j.1432-1033.1985.tb08859.x - J. Moll. cell. cardiol. v.31 Primary endothelial dysfunction: Atherosclerosis. Shimokawa, H. https://doi.org/10.1006/jmcc.1998.0839
- J. Vasc Res. v.34 Calcium-dependent and -independent activation of the endothelial NO synthase. Fleming, I.;Bauersachs, J.;Busse, R. https://doi.org/10.1159/000159220
- J. Moll cell cardiol. v.31 NO: the primary EDRF. Fleming, I.;Busse, R. https://doi.org/10.1006/jmcc.1998.0840
- J. Moll cell cardiol. v.31 The alternative: EDHF F l tou, M.;Vanhoutte, P. M. https://doi.org/10.1006/jmcc.1998.0840
- Am. J. Physiol. Heart circ. Physiol. v.278 In eNOS knockout mice skeletal muscle arteriolar dilation to acetylchorine is mediated by EDHF. Huang, A.;Sun, D.;Smith, C. J.;Counetta, J. A.;Shesely, E. G.;Koller, A.;Kaley, G.
- Am. J. Physiol. v.273 Components of acetylcholine-induced dilation in isolated rat arterioles. Bakker, E. N. T. P.;Sipkema, P.
- FASEB J. v.3 no.1 Endothelium-derived nitric oxide: action and properties. Ignarro, L. J.
- Pharmacology. Rang, H. P.;Dale, M. M.;Ritter, J. M.
- Eur. J. Pharm. v.274 Endothelium -dependent relaxation resistant to NG-nitro-L-arginine in rat aorta. Hadake, K.;Wakabayashi, I.;Hishda, S. https://doi.org/10.1016/0014-2999(94)00704-B
- Cicr Res v.83 A major role for prostacyclin in nitric oxide-induced occular vasorelaxation in the piglet. Hardy, P.;Abran, D.;Hou, X.;Lahaie, I.;Peri, K. G.;Asselin, P.;Varma, D. R.;Chemtob, S. https://doi.org/10.1161/01.RES.83.7.721
- News in the Physiological science. v.15 Endothelium-derived hyperpolarizing factor - fact or fiction? Hecker, M.
- Planta Med. v.65 Scopoletin: an inducible nitric oxide synthesis inhibitory active constituent from Artemisia feddei. Kang, T. H.;Pae, H. O.;Jeong, S. J.;Yoo, J. C.;Choi, B. M.;Jun, C. D.;Chung, H. T.; Miyamotm, R.;Higuchi, R.;Kim, Y. C.
- Planta Med. v.65 In vitro inducible nitric oxide synthesis inhibitory active constituents from Fraxinus rhynchophylla. Kang, T. H.;Pae, H. O.;Ko, Y. S.;Yoo, J. C.;Choi, B. M.;Jun, C. D.;Chung, H. T.; Inagaki, M.;Higuchi, R.;Kim, Y. C. https://doi.org/10.1055/s-2006-960840
- Japan. J. Pharmacol. v.31 Choleretic effect of Artemisia capllaris extract in rats. Okuno, I.;uchida, K.;Kadowaki, M.;Akahori, A. https://doi.org/10.1254/jjp.31.835
- Biol. Pharmacol. Bull. v.17 no.1 Production of holeretic substances in the capitulum, leaf and stem of Artemisia capillaris during the plant growth cycle. Ikenaga, T.;Hizaco, M.;Tajima, M.;Nakayama, K. https://doi.org/10.1248/bpb.17.150
- Arch. Pharmacol. Res. v.21 no.6 Hepatoprotective activity of scopoletin, a constituent of Solarum lyratum. Kang, S. Y.;Sung, S.H.;Park, J. H.;Kim, Y. C. https://doi.org/10.1007/BF02976764
- Planta Med. no.1 Antihepatotoxic principles of Artemisia capillaris buds. Kiso, Y.;Ogasawara, S.;Hirota, K.;Watanabe, N.;Oshima, Y.;Konno, C.;Hikino, H.
- Free radical biology & Medicine. v.28 no.11 Hydrogen peroxide release from human eosinophils on fibronectin: scopoletin enhances eosinophil activation. Raible, D. G.;Mohanty, J. G.;Jaffe, J. S.;Stella, H. J.;Sprenkle, B. E.;Glaum, M. C.; Schulmann, E. S. https://doi.org/10.1016/S0891-5849(00)00279-3
- Anesthesiology. v.84 Etomidate and thiopental inhibit the release of endothelium-derived hyperpolarizing factor in the human renal artery. Kessler, P.;Lischke, V.;Hecker, M. https://doi.org/10.1097/00000542-199606000-00025
- FEBS lett. v.265 Calcium-dependent nitric oxide synthesis in endothelial cytosol is mediated by calmodulin. Busse, R.;Műlsch, A. https://doi.org/10.1016/0014-5793(90)80902-U
-
Eur. J. Pharmacol.
v.366
Agonist -dependent difference in the relationship between cytosolic Ca
$^{2+}$ level and release of vascular relaxing factor in the endothelium of rabbit aortic valve. Amano, K.;Hori, M.;Ozaki, H.;Karaki, H. https://doi.org/10.1016/S0014-2999(98)00913-3 - J. Clin. Invest. v.88 no.5 Flow activates an endothelial potassium channel to release an endogenous nitrovasodilator. Coke, J. P.;Rossitch, E. Jr.;Andon, N. A.;Dazu, V. J. https://doi.org/10.1172/JCI115481
- J. Moll cell cardiol. v.28 Hydroxyl radical - a mediator of acetylcholine- induced vascular relaxtion. Prasad, K.;Bharadwaj, L. A. https://doi.org/10.1006/jmcc.1996.0196
- Eur. J. Pharmacol. v.392 Time course of changes in endothelium -dependent and -independent relaxation of chronically diabetic aorta: role of reactive oxygen species. Karasu, C. https://doi.org/10.1016/S0014-2999(00)00140-0
- J. pathol. v.190 no.3 U. Nitric oxide in the pathogenesis of vascular disease. Li, H. Forstermann https://doi.org/10.1002/(SICI)1096-9896(200002)190:3<244::AID-PATH575>3.0.CO;2-8