SÁNDOR, Roman, Jiří SLANINA, Adam MIDLIK, Kristýna ŠEBRLOVÁ, Lucie NOVOTNÁ, Martina ČARNECKÁ, Iva SLANINOVÁ, Petr TÁBORSKÝ, Eva TÁBORSKÁ and Ondřej PEŠ. Sanguinarine is reduced by NADH through a covalent adduct. Phytochemistry. Oxford: Pergamon-Elsevier Science LTD, vol. 145, JAN 2018, p. 77-84. ISSN 0031-9422. doi:10.1016/j.phytochem.2017.10.010. 2018.
Other formats:   BibTeX LaTeX RIS
Basic information
Original name Sanguinarine is reduced by NADH through a covalent adduct
Authors SÁNDOR, Roman (703 Slovakia, belonging to the institution), Jiří SLANINA (203 Czech Republic, belonging to the institution), Adam MIDLIK (703 Slovakia, belonging to the institution), Kristýna ŠEBRLOVÁ (203 Czech Republic, belonging to the institution), Lucie NOVOTNÁ (203 Czech Republic, belonging to the institution), Martina ČARNECKÁ (703 Slovakia, belonging to the institution), Iva SLANINOVÁ (203 Czech Republic, belonging to the institution), Petr TÁBORSKÝ (203 Czech Republic, belonging to the institution), Eva TÁBORSKÁ (203 Czech Republic, belonging to the institution) and Ondřej PEŠ (203 Czech Republic, guarantor, belonging to the institution).
Edition Phytochemistry, Oxford, Pergamon-Elsevier Science LTD, 2018, 0031-9422.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10608 Biochemistry and molecular biology
Country of publisher United Kingdom of Great Britain and Northern Ireland
Confidentiality degree is not subject to a state or trade secret
Impact factor Impact factor: 2.905
RIV identification code RIV/00216224:14110/18:00102093
Organization unit Faculty of Medicine
Doi http://dx.doi.org/10.1016/j.phytochem.2017.10.010
UT WoS 000423245300009
Keywords in English Benzophenanthridine alkaloids; Ene adduct; Hydride transfer; LC-MS; NADH; NADH depletion; Redox cycling; Sanguinarine
Tags 14110512, 14110513, EL OK, podil, rivok
Tags International impact, Reviewed
Changed by Changed by: Soňa Böhmová, učo 232884. Changed: 2/5/2019 13:05.
Abstract
Sanguinarine is a benzo[c]phenanthridine alkaloid with interesting cytotoxic properties, such as induction of oxidative DNA damage and very rapid apoptosis, which is not mediated by p53-dependent signaling. It has been previously documented that sanguinarine is reduced with NADH even in absence of any enzymes while being converted to its dihydro form. We found that the dark blue fluorescent species, observed during sanguinarine reduction with NADH and misinterpreted by Matkar et al. (Arch. Biochem. Biophys. 2008, 477, 43–52) as an anionic form of the alkaloid, is a covalent adduct formed by the interaction of NADH and sanguinarine. The covalent adduct is then converted slowly to the products, dihydrosanguinarine and NAD+, in the second step of reduction. The product of the reduction, dihydrosanguinarine, was continually re-oxidized by the atmospheric oxygen back to sanguinarine, resulting in further reacting with NADH and eventually depleting all NADH molecules. The ability of sanguinarine to diminish the pool of NADH and NADPH is further considered when explaining the sanguinarine-induced apoptosis in living cells.
Links
MUNI/A/0810/2016, interní kód MUName: Molekulární a buněčná biologie
Investor: Masaryk University, Category A
MUNI/A/1205/2016, interní kód MUName: Příspěvek biochemických metodik ke studiu molekulární podstaty vybraných patologických stavů a onemocnění (Acronym: mopopas)
Investor: Masaryk University, Category A
MUNI/A/1237/2016, interní kód MUName: Vývoj metod a instrumentace pro analýzu biologicky významných látek 2017
Investor: Masaryk University, Category A
PrintDisplayed: 18/4/2024 21:46