Zobrazeno 1 - 10
of 43
pro vyhledávání: '"M V Kindt"'
Publikováno v:
Digestive Diseases and Sciences. 43:1009-1015
Bisphosphonates have generally few clinical adverse effects, the most common being gastrointestinal disturbances. It is generally believed that bisphosphonates with a primary amine are more irritating to the gastrointestinal tract than those without
Publikováno v:
Toxicologic Pathology. 23:606-619
L-694,492 (DUP 532), an angiotensin II (AII) receptor antagonist, was given orally at 125 mg/kh/day to rats and monkeys for up to 6 mo to assess the effects of the compound on juxtaglomerular (JG) cells. In rats, mild JG cell hypertrophy/hyperplasia
Publikováno v:
Digestive diseases and sciences. 43(5)
Bisphosphonates have generally few clinical adverse effects, the most common being gastrointestinal disturbances. It is generally believed that bisphosphonates with a primary amine are more irritating to the gastrointestinal tract than those without
Autor:
Jentsch, Valerie L.1 (AUTHOR) valerie.jentsch@rub.de, Wolf, Oliver T.1 (AUTHOR), Otto, Tobias1 (AUTHOR), Merz, Christian J.1 (AUTHOR)
Publikováno v:
Psychophysiology. Nov2023, Vol. 60 Issue 11, p1-19. 19p.
Autor:
Roger C. Duvoisin, Stephen K. Youngster, Arthur Hess, M V Kindt, Patricia K. Sonsalla, Richard E. Heikkila
Publikováno v:
European Journal of Pharmacology. 122:283-287
The administration to mice of 1-methyl-4-(2′-methylphenyl)-1,2,3,6-tetrahydropyridine (2′-CH3-MPTP), a substituted analog of the dopaminergic neurotoxin MPTP caused even more dopaminergic toxicity than MPTP itself. Under conditions in which MPTP
Autor:
Starita, Francesca1 (AUTHOR) francesca.starita2@unibo.it, Pirazzini, Gabriele2 (AUTHOR), Ricci, Giulia2 (AUTHOR), Garofalo, Sara1 (AUTHOR), Dalbagno, Daniela1 (AUTHOR), Degni, Luigi A. E.1 (AUTHOR), Di Pellegrino, Giuseppe1 (AUTHOR), Magosso, Elisa2 (AUTHOR), Ursino, Mauro2 (AUTHOR)
Publikováno v:
Psychophysiology. Jul2023, Vol. 60 Issue 7, p1-18. 18p. 4 Diagrams, 2 Charts, 6 Graphs.
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 242(3)
1-Methyl-4-(2'-methylphenyl)-1,2,3,6-tetrahydropyridine (2'CH3-MPTP) was shown previously to be a more potent neurotoxicant than 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) in mice. The present investigation was conducted to determine possibl
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 242(3)
In previous studies and in the accompanying paper, 1-methyl-4-(2'-methylphenyl)-1,2,3,6-tetrahydropyridine (2'CH3-MPTP) was found to be more potent than MPTP in producing dopaminergic neurotoxicity in mice. One purpose of the present study was to det
Publikováno v:
Life sciences. 40(8)
1-Methyl-4-phenylpyridinium (MPP+), the putative toxic metabolite of the neurotoxin, 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP), inhibited NAD(H)-linked mitochondrial oxidation at the level of Complex I of the electron transport system. MPTP
Autor:
Hisahara, Shin1, Shimohama, Shun1 shimoha@sapmed.ac.jp
Publikováno v:
Parkinson's Disease (20420080). 2011, p1-14. 14p. 3 Charts.