-
2
-
-
0023748529
-
Melatonin
-
Arendt J (1988) Melatonin. Clin Endocrinol 29: 205-229
-
(1988)
Clin Endocrinol
, vol.29
, pp. 205-229
-
-
Arendt, J.1
-
3
-
-
0001632363
-
Melatonin's multifarious marvels: Miracle or myth?
-
Bonn D (1996) Melatonin's multifarious marvels: miracle or myth? Lancet 347: 184
-
(1996)
Lancet
, vol.347
, pp. 184
-
-
Bonn, D.1
-
4
-
-
0030430033
-
Cytochrome P450 isoform inhibitors as a tool for the investigation of metabolic reactions catalyzed by human liver microsomes
-
Bourrié M, Meunier V, Berger Y, Fahre G (1996) Cytochrome P450 isoform inhibitors as a tool for the investigation of metabolic reactions catalyzed by human liver microsomes. J Pharmacol Exp Ther 277: 321-332
-
(1996)
J Pharmacol Exp Ther
, vol.277
, pp. 321-332
-
-
Bourrié, M.1
Meunier, V.2
Berger, Y.3
Fahre, G.4
-
5
-
-
0027406654
-
Fluvoxamine is a potent inhibitor of cytochrome P4501A2
-
Brøsen K, Skjelbo E, Rasmussen BB, Poulson HE, Loft S (1993) Fluvoxamine is a potent inhibitor of cytochrome P4501A2. Biochem Pharmacol 45: 1211-1214
-
(1993)
Biochem Pharmacol
, vol.45
, pp. 1211-1214
-
-
Brøsen, K.1
Skjelbo, E.2
Rasmussen, B.B.3
Poulson, H.E.4
Loft, S.5
-
6
-
-
0031021914
-
Melatonin in humans
-
Brzezinski A (1997) Melatonin in humans. N Engl J Med 336: 186-195
-
(1997)
N Engl J Med
, vol.336
, pp. 186-195
-
-
Brzezinski, A.1
-
7
-
-
0033638766
-
The absolute bioavailability of oral melatonin
-
DeMuro RL, Nafziger AN, Blask DE, Menhinick AM, Bertino JS (2000) The absolute bioavailability of oral melatonin. J Clin Pharmacol 40: 781-784
-
(2000)
J Clin Pharmacol
, vol.40
, pp. 781-784
-
-
DeMuro, R.L.1
Nafziger, A.N.2
Blask, D.E.3
Menhinick, A.M.4
Bertino, J.S.5
-
9
-
-
0032942865
-
The pineal and extra-pineal origins of 5-sulphatoxy N-acetyl-serolonin in humans
-
Di WL, Djahanbakhch O, Kadva A, Street C, Silman R (1999) The pineal and extra-pineal origins of 5-sulphatoxy N-acetyl-serolonin in humans. J Pineal Res 26: 221-226
-
(1999)
J Pineal Res
, vol.26
, pp. 221-226
-
-
Di, W.L.1
Djahanbakhch, O.2
Kadva, A.3
Street, C.4
Silman, R.5
-
10
-
-
0030899603
-
Inhibition by omeprazole of proguanil metabolism: Mechanism of the interaction in vitro and prediction of in vivo results from the in vitro experiments
-
Funck-Brentano C, Becquemont L, Lenevu A, Roux A, Jaillon P, Beaune P (1997) Inhibition by omeprazole of proguanil metabolism: mechanism of the interaction in vitro and prediction of in vivo results from the in vitro experiments. J Pharmacol Exp Ther 280: 730-738
-
(1997)
J Pharmacol Exp Ther
, vol.280
, pp. 730-738
-
-
Funck-Brentano, C.1
Becquemont, L.2
Lenevu, A.3
Roux, A.4
Jaillon, P.5
Beaune, P.6
-
11
-
-
0033964363
-
Increased bioavailability of oral melatonin after fluvoxamine coadministration
-
Härtter S, Grözinger M, Weigamnn H, Röschke J, Hiemke C (2000) Increased bioavailability of oral melatonin after fluvoxamine coadministration. Clin Pharmacol Ther 67: 1-6
-
(2000)
Clin Pharmacol Ther
, vol.67
, pp. 1-6
-
-
Härtter, S.1
Grözinger, M.2
Weigamnn, H.3
Röschke, J.4
Hiemke, C.5
-
12
-
-
12644276395
-
Fluvoxamine inhibits the CYP2C19 catalyzed bioactivation of chloroguanide
-
Jeppesen U, Skjelbo E, Rasmussen B, Poulsen HE, Loft S (1997) Fluvoxamine inhibits the CYP2C19 catalyzed bioactivation of chloroguanide. Clin Pharmacol Ther 62: 279-286
-
(1997)
Clin Pharmacol Ther
, vol.62
, pp. 279-286
-
-
Jeppesen, U.1
Skjelbo, E.2
Rasmussen, B.3
Poulsen, H.E.4
Loft, S.5
-
13
-
-
0026094528
-
Use of caffeine metabolic ratios to explore CYP1A2 and xanthine oxidase activities
-
Kalow W, Tang B-K (1991) Use of caffeine metabolic ratios to explore CYP1A2 and xanthine oxidase activities. Clin Pharmacol Ther 50: 508-519
-
(1991)
Clin Pharmacol Ther
, vol.50
, pp. 508-519
-
-
Kalow, W.1
Tang, B.-K.2
-
14
-
-
0028600597
-
The importance of substrate concentration in determining cytochromes P450 therapeutically relevant in vivo
-
Kato R, Yamazoe Y (1994) The importance of substrate concentration in determining cytochromes P450 therapeutically relevant in vivo. Pharmacogenetics 4: 359-362
-
(1994)
Pharmacogenetics
, vol.4
, pp. 359-362
-
-
Kato, R.1
Yamazoe, Y.2
-
15
-
-
14444282584
-
Identification of cytochrome P450 isoforms involved in citalopram N-demethylation by human liver microsomes
-
Kobayashi K, Chiba K, Yagi T, Shimada N, Taniguchi T, Horie T, Tani M, Yamamoto T, Ishizaki T, Kuroiwa Y (1997) Identification of cytochrome P450 isoforms involved in citalopram N-demethylation by human liver microsomes. J Pharmacol Exp Ther 280: 927-933
-
(1997)
J Pharmacol Exp Ther
, vol.280
, pp. 927-933
-
-
Kobayashi, K.1
Chiba, K.2
Yagi, T.3
Shimada, N.4
Taniguchi, T.5
Horie, T.6
Tani, M.7
Yamamoto, T.8
Ishizaki, T.9
Kuroiwa, Y.10
-
17
-
-
0022388062
-
Pharmacokinetics of melatonin in man1: First pass hepatic metabolism
-
Lane EA, Moss HB (1985) Pharmacokinetics of melatonin in man1: first pass hepatic metabolism. J Clin Endocrinol Metab 61: 1214-1216
-
(1985)
J Clin Endocrinol Metab
, vol.61
, pp. 1214-1216
-
-
Lane, E.A.1
Moss, H.B.2
-
18
-
-
0021361426
-
Melatonin can be differentially metabolized in the rat to produce N-acetylserotonin in addition to 6-hydroxy-melatonin
-
Leone RM, Silman RE (1984) Melatonin can be differentially metabolized in the rat to produce N-acetylserotonin in addition to 6-hydroxy-melatonin. Endocrinology 114: 1825-1832
-
(1984)
Endocrinology
, vol.114
, pp. 1825-1832
-
-
Leone, R.M.1
Silman, R.E.2
-
20
-
-
0031841377
-
Cytochrome P4502C9: An enzyme of major importance in human drug metabolism
-
Miners JO, Birkett DJ (1998). Cytochrome P4502C9: an enzyme of major importance in human drug metabolism. Br J Clin Pharmacol 45: 525-538
-
(1998)
Br J Clin Pharmacol
, vol.45
, pp. 525-538
-
-
Miners, J.O.1
Birkett, D.J.2
-
21
-
-
0028858960
-
Cytochrome P450 inhibitors: Evaluation of specificities in the in vitro metabolism of therapeutic agents by human liver microsomes
-
Newton DJ, Wang RW, Lu A (1995) Cytochrome P450 inhibitors: evaluation of specificities in the in vitro metabolism of therapeutic agents by human liver microsomes. Drug Metab Dispos 23: 154-158
-
(1995)
Drug Metab Dispos
, vol.23
, pp. 154-158
-
-
Newton, D.J.1
Wang, R.W.2
Lu, A.3
-
22
-
-
0031438162
-
A combination of mutations in the CYP2D6*17 (CYP2D6Z) allele causes alterations in enzyme function
-
Oscarson M, Hidestrand M, Johansson I, Ingelman-Sundberg M (1997) A combination of mutations in the CYP2D6*17 (CYP2D6Z) allele causes alterations in enzyme function. Mol Pharmacol 52: 1034-1040
-
(1997)
Mol Pharmacol
, vol.52
, pp. 1034-1040
-
-
Oscarson, M.1
Hidestrand, M.2
Johansson, I.3
Ingelman-Sundberg, M.4
-
23
-
-
0028080304
-
Inhibition of diazepam metabolism by fluvoxamine: A pharmakinetic study in normal volunteers
-
Perucca E, Gatti G, Cipolla G, Spina E, Barel S, Soback S, Gips M, Bialer M (1994) Inhibition of diazepam metabolism by fluvoxamine: a pharmakinetic study in normal volunteers. Clin Pharmacol Ther 56: 471-476
-
(1994)
Clin Pharmacol Ther
, vol.56
, pp. 471-476
-
-
Perucca, E.1
Gatti, G.2
Cipolla, G.3
Spina, E.4
Barel, S.5
Soback, S.6
Gips, M.7
Bialer, M.8
-
24
-
-
0027253005
-
A double-blind trial of melatonin as a treatment for jet lag in international cabin crew
-
Petrie K, Dawson AG, Thompson L, Brook R (1993) A double-blind trial of melatonin as a treatment for jet lag in international cabin crew. Biol Psychiatry 33: 526-530
-
(1993)
Biol Psychiatry
, vol.33
, pp. 526-530
-
-
Petrie, K.1
Dawson, A.G.2
Thompson, L.3
Brook, R.4
-
25
-
-
0031742883
-
Fluvoxamine is a potent inhibitor of the metabolism of caffeine in vitro
-
Rasmussen BB, Nielsen TL, Brøsen K (1998) Fluvoxamine is a potent inhibitor of the metabolism of caffeine in vitro. Pharmacol Toxicol 83: 240-245
-
(1998)
Pharmacol Toxicol
, vol.83
, pp. 240-245
-
-
Rasmussen, B.B.1
Nielsen, T.L.2
Brøsen, K.3
-
26
-
-
0028784799
-
The role of the neurohormone melatonin as a buffer against macromolecular oxidative damage
-
Reiter RJ (1995) The role of the neurohormone melatonin as a buffer against macromolecular oxidative damage. Neurochem Int 27: 453-460
-
(1995)
Neurochem Int
, vol.27
, pp. 453-460
-
-
Reiter, R.J.1
-
27
-
-
0030778136
-
Sleep-promoting effects of melatonin: At what dose, in whom, under what conditions, and by what mechanisms?
-
Sack RL, Hughes RJ, Edgar DM, Lewy AJ (1997) Sleep-promoting effects of melatonin: at what dose, in whom, under what conditions, and by what mechanisms? Sleep 20: 908-915
-
(1997)
Sleep
, vol.20
, pp. 908-915
-
-
Sack, R.L.1
Hughes, R.J.2
Edgar, D.M.3
Lewy, A.J.4
-
28
-
-
0029934305
-
Enzyme kinetic modelling as a tool to analyse the behaviour of cytochrome P450 catalysed reactions: Application to amitriptyline N-demethylation
-
Schmider J, Greenblatt DJ, Harmatz JS, Shader R (1996) Enzyme kinetic modelling as a tool to analyse the behaviour of cytochrome P450 catalysed reactions: application to amitriptyline N-demethylation. Br J Clin Pharmacol 41: 593-604
-
(1996)
Br J Clin Pharmacol
, vol.41
, pp. 593-604
-
-
Schmider, J.1
Greenblatt, D.J.2
Harmatz, J.S.3
Shader, R.4
-
29
-
-
0030706197
-
Inhibition of CYP2C9 by selective serotonin reuptake inhibitors in vitro: Studies of phenytoin para-hydroxylation
-
Schmider J, Greenblatt DJ, von Moltke LL, Karsov D, Shader RI (1997) Inhibition of CYP2C9 by selective serotonin reuptake inhibitors in vitro: studies of phenytoin para-hydroxylation. Br J Clin Pharmacol 44: 495-498
-
(1997)
Br J Clin Pharmacol
, vol.44
, pp. 495-498
-
-
Schmider, J.1
Greenblatt, D.J.2
Von Moltke, L.L.3
Karsov, D.4
Shader, R.I.5
-
30
-
-
0028352671
-
Comparison of the effects of acute fluvoxamine and desipramine administration on melatonin and cortisol production in humans
-
Skene DJ, Bojkowski CJ, Arendt J (1994) Comparison of the effects of acute fluvoxamine and desipramine administration on melatonin and cortisol production in humans. Br J clin Pharmacol 37: 181-186
-
(1994)
Br J Clin Pharmacol
, vol.37
, pp. 181-186
-
-
Skene, D.J.1
Bojkowski, C.J.2
Arendt, J.3
-
31
-
-
0002979059
-
Melatonin: A potent, endogenous hydroxyl radical scavenger
-
Tan DX, Chen LD, Poeggeler B, Manchester LC, Reiter RJ (1993a) Melatonin: a potent, endogenous hydroxyl radical scavenger. Endocr J 1: 57-60
-
(1993)
Endocr J
, vol.1
, pp. 57-60
-
-
Tan, D.X.1
Chen, L.D.2
Poeggeler, B.3
Manchester, L.C.4
Reiter, R.J.5
-
32
-
-
0027201993
-
The pineal hormone melatonin inhibits DNA-adduct formation induced by the chemical carcinogen safrole in vivo
-
Tan DX, Poeggeler B, Reiter RJ, Chen LD, Chen S, Manchester LC, Barlow-Walden LR (1993b) The pineal hormone melatonin inhibits DNA-adduct formation induced by the chemical carcinogen safrole in vivo. Cancer Lett 70: 65-71
-
(1993)
Cancer Lett
, vol.70
, pp. 65-71
-
-
Tan, D.X.1
Poeggeler, B.2
Reiter, R.J.3
Chen, L.D.4
Chen, S.5
Manchester, L.C.6
Barlow-Walden, L.R.7
-
33
-
-
0030094638
-
Theophylline metabolism in human liver microsomes: Inhibition studies
-
Tjia JF, Colbert J, Back DJ (1996) Theophylline metabolism in human liver microsomes: inhibition studies. J Pharmacol Exp Ther 276: 912-917
-
(1996)
J Pharmacol Exp Ther
, vol.276
, pp. 912-917
-
-
Tjia, J.F.1
Colbert, J.2
Back, D.J.3
-
34
-
-
0027480346
-
Enhanced in vivo monooxygenase activities of mammalian P450s in engineered yeast cells producing high levels of NADPH-P450 reductase and human cytochrome b5
-
Truan G, Cullin C, Reisdorf P, Urban P, Pompon D (1993) Enhanced in vivo monooxygenase activities of mammalian P450s in engineered yeast cells producing high levels of NADPH-P450 reductase and human cytochrome b5. Gene 125: 49-55
-
(1993)
Gene
, vol.125
, pp. 49-55
-
-
Truan, G.1
Cullin, C.2
Reisdorf, P.3
Urban, P.4
Pompon, D.5
-
35
-
-
0018897519
-
Drug metabolism in human liver in vitro: Establishment of a liver bank
-
von Bahr C, Groth CG, Jansson H, Lundgren G, Lind M, Glauman H (1980) Drug metabolism in human liver in vitro: establishment of a liver bank. Clin Pharmacol Ther 27: 711-725
-
(1980)
Clin Pharmacol Ther
, vol.27
, pp. 711-725
-
-
Von Bahr, C.1
Groth, C.G.2
Jansson, H.3
Lundgren, G.4
Lind, M.5
Glauman, H.6
-
36
-
-
0034129702
-
Fluvoxamine, but not citalopram, increases serum melatonin in healthy subjects
-
von Bahr C, Ursing C, Yasui N, Tybring G, Bertilsson L, Röjdmark S (2000) Fluvoxamine, but not citalopram, increases serum melatonin in healthy subjects. Eur J Clin Pharmacol 56: 123-127
-
(2000)
Eur J Clin Pharmacol
, vol.56
, pp. 123-127
-
-
Von Bahr, C.1
Ursing, C.2
Yasui, N.3
Tybring, G.4
Bertilsson, L.5
Röjdmark, S.6
-
37
-
-
0028898816
-
Inhibition of alprazolam and desipramine hydroxylation in vitro by paroxetine and fluvoxamine: Comparison with other selective serotonin reuptake inhibitors antidepressant
-
von Moltke LL, Greenblatt DJ, Court MH, Duan SX, Harmatz JS, Shader RJ (1995) Inhibition of alprazolam and desipramine hydroxylation in vitro by paroxetine and fluvoxamine: comparison with other selective serotonin reuptake inhibitors antidepressant. J Clin Psychopharmacol 15: 125-131
-
(1995)
J Clin Psychopharmacol
, vol.15
, pp. 125-131
-
-
Von Moltke, L.L.1
Greenblatt, D.J.2
Court, M.H.3
Duan, S.X.4
Harmatz, J.S.5
Shader, R.J.6
-
38
-
-
0021225301
-
Unavailability of oral melatonin in humans
-
Waldhauser F, Waldhauser M, Lieberman HR, Deng M-H, Lynch HJ, Wurtman RJ (1984) Unavailability of oral melatonin in humans. Neuroendocrinology 39: 307-313
-
(1984)
Neuroendocrinology
, vol.39
, pp. 307-313
-
-
Waldhauser, F.1
Waldhauser, M.2
Lieberman, H.R.3
Deng, M.-H.4
Lynch, H.J.5
Wurtman, R.J.6
-
40
-
-
0344061546
-
N-acetylserotonin is a better extra- And intracellular antioxidant than melatonin
-
Wolfler A, Abuja PM, Schauenstein K, Liebmann PM (1999) N-acetylserotonin is a better extra- and intracellular antioxidant than melatonin. FEBS Lett 449: 206-210
-
(1999)
FEBS Lett
, vol.449
, pp. 206-210
-
-
Wolfler, A.1
Abuja, P.M.2
Schauenstein, K.3
Liebmann, P.M.4
-
41
-
-
0029824249
-
In vivo inhibition of CYP2C19 but not CYP2D6 by fluvoxamine
-
Xu Z-H, Xie H-G, Zhou H-H (1996) In vivo inhibition of CYP2C19 but not CYP2D6 by fluvoxamine. Br J Clin Pharmacol 42: 518-521
-
(1996)
Br J Clin Pharmacol
, vol.42
, pp. 518-521
-
-
Xu, Z.-H.1
Xie, H.-G.2
Zhou, H.-H.3
|