R Sustmann
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Explore the profile of R Sustmann including associated specialties, affiliations and a list of published articles.
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Articles
10
Citations
72
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Recent Articles
1.
Pamp K, Kerkweg U, Korth H, Homann F, Rauen U, Sustmann R, et al.
Biochimie
. 2008 Jul;
90(10):1591-601.
PMID: 18627785
The enzymatic system mainly responsible for the reduction of labile iron ions in mammalian cells is still unknown. Using isolated organelles of the rat liver, i.e. mitochondria, microsomes, nuclei and...
2.
Paschke J, Kirsch M, Korth H, De Groot H, Sustmann R
J Am Chem Soc
. 2001 Nov;
123(44):11099-100.
PMID: 11686730
No abstract available.
3.
Kirsch M, Lehnig M, Korth H, Sustmann R, De Groot H
Chemistry
. 2001 Sep;
7(15):3313-20.
PMID: 11531117
Peroxynitrite (ONOO-/ONOOH) is assumed to react preferentially with carbon dioxide in vivo to produce nitrogen dioxide (NO2*) and trioxocarbonate(1-) (CO3*-) radicals. We have studied the mechanism by which glutathione (GSH)...
4.
Kirsch M, Korth H, Sustmann R, De Groot H
Chem Res Toxicol
. 2000 Jun;
13(6):451-61.
PMID: 10858318
Hydrogen carbonate (bicarbonate, HCO(3)(-)) has been proposed to accelerate the decomposition of N(2)O(3) because N-nitrosation of morpholine via a nitric oxide/oxygen mixture ((*)NO/O(2)) was inhibited by the addition of HCO(3)(-)...
5.
Batz M, Korth H, Meineke P, Sustmann R
Methods Enzymol
. 1999 Jan;
301:532-9.
PMID: 9919601
No abstract available.
6.
Kirsch M, Lomonosova E, Korth H, Sustmann R, De Groot H
J Biol Chem
. 1998 May;
273(21):12716-24.
PMID: 9582295
Organic amine-based buffer compounds such as HEPES (Good's buffers) are commonly applied in experimental systems, including those where the biological effects of peroxynitrite are studied. In such studies 3-morpholinosydnonimine N-ethylcarbamide...
7.
Ioannidis I, Batz M, Kirsch M, Korth H, Sustmann R, De Groot H
Biochem J
. 1998 Feb;
329 ( Pt 2):425-30.
PMID: 9425128
Cultured rat liver endothelial cells were incubated with 1 and 2 mM spermineNONOate at different O2 concentrations in the incubation atmosphere. (Z)-1-{N-[3-Aminopropyl]-N-[4-(3-aminopropylammonio) butyl]-amino}diazen-1-ium-1,2- diolate (spermineNONOate), at 2 mM, was highly...
8.
Rauen U, Elling B, Gizewski E, Korth H, Sustmann R, De Groot H
Free Radic Biol Med
. 1997 Jan;
22(1-2):17-24.
PMID: 8958126
We have previously demonstrated an energy-dependent injury to cultured liver endothelial cells during cold incubation in University of Wisconsin (UW) solution. In the present study, we report experimental evidence for...
9.
Ioannidis I, Batz M, Paul T, Korth H, Sustmann R, De Groot H
Biochem J
. 1996 Sep;
318 ( Pt 3):789-95.
PMID: 8836121
S-Nitroso-N-acetyl-DL-penicillamine (SNAP) and sodium nitroprusside (SNP), both of which are known to release nitric oxide (.NO), exhibited cytotoxicity against cultivated endothelial cells. Under hypoxic conditions 5 mM SNAP and 20...
10.
Korth H, Sustmann R, Thater C, Butler A, Ingold K
J Biol Chem
. 1994 Jul;
269(27):17776-9.
PMID: 7517932
The mechanism of oxidation of N omega-hydroxyl-L-arginine (NHA) by the iron-dioxygen complex in nitric oxide synthase (NOS) is still uncertain. The uncertainty has not been helped by a lack of...