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Pregled bibliografske jedinice broj: 876366

Rational Design of Superoxide Dismutase (SOD) Mimics: The Evaluation of the Therapeutic Potential of New Cationic Mn Porphyrins with Linear and Cyclic Substituents


Tovmasyan, Artak; Carballal, Sebastian; Ghazaryan, Robert; Melikyan, Lida; Weitner, Tin; Maia, Clarissa G. C.; Reboucas, Julio S.; Radi, Rafael; Spasojević, Ivan; Benov, Ludmil et al.
Rational Design of Superoxide Dismutase (SOD) Mimics: The Evaluation of the Therapeutic Potential of New Cationic Mn Porphyrins with Linear and Cyclic Substituents // Inorganic chemistry, 53 (2014), 21; 11467-11483 doi:10.1021/ic501329p (međunarodna recenzija, članak, znanstveni)


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Naslov
Rational Design of Superoxide Dismutase (SOD) Mimics: The Evaluation of the Therapeutic Potential of New Cationic Mn Porphyrins with Linear and Cyclic Substituents

Autori
Tovmasyan, Artak ; Carballal, Sebastian ; Ghazaryan, Robert ; Melikyan, Lida ; Weitner, Tin ; Maia, Clarissa G. C. ; Reboucas, Julio S. ; Radi, Rafael ; Spasojević, Ivan ; Benov, Ludmil ; Batinić-Haberle ; Ines

Izvornik
Inorganic chemistry (0020-1669) 53 (2014), 21; 11467-11483

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
Mn porphyrins ; redox properties ; lipophilicity ; therapeutic potential

Sažetak
Our goal herein has been to gain further insight into the parameters which control porphyrin therapeutic potential. Mn porphyrins (MnTnOct-2-PyP5+, MnTnHexOE-2-PyP5+, MnTE-2- PyPhP5+, and MnTPhE-2-PyP5+) that bear the same positive charge and same number of carbon atoms at meso positions of porphyrin core were explored. The carbon atoms of their meso substituents are organized to form either linear or cyclic structures of vastly different redox properties, bulkiness, and lipophilicities. These Mn porphyrins were compared to frequently studied compounds, MnTE- 2-PyP5+, MnTE-3-PyP5+, and MnTBAP3–. All Mn(III) porphyrins (MnPs) have metal-centered reduction potential, E1/2 for MnIIIP/MnIIP redox couple, ranging from −194 to +340 mV versus NHE, log kcat(O2•–) from 3.16 to 7.92, and log kred(ONOO–) from 5.02 to 7.53. The lipophilicity, expressed as partition between n-octanol and water, log POW, was in the range −1.67 to −7.67. The therapeutic potential of MnPs was assessed via: (i) in vitro ability to prevent spontaneous lipid peroxidation in rat brain homogenate as assessed by malondialdehyde levels ; (ii) in vivo O2•– specific assay to measure the efficacy in protecting the aerobic growth of SOD-deficient Saccharomyces cerevisiae ; and (iii) aqueous solution chemistry to measure the reactivity toward major in vivo endogenous antioxidant, ascorbate. Under the conditions of lipid peroxidation assay, the transport across the cellular membranes, and in turn shape and size of molecule, played no significant role. Those MnPs of E1/2 ∼ +300 mV were the most efficacious, significantly inhibiting lipid peroxidation in 0.5–10 μM range. At up to 200 μM, MnTBAP3– (E1/2 = −194 mV vs NHE) failed to inhibit lipid peroxidation, while MnTE-2- PyPhP5+ with 129 mV more positive E1/2 (−65 mV vs NHE) was fully efficacious at 50 μM. The E1/2 of MnIIIP/MnIIP redox couple is proportional to the log kcat(O2•–), i.e., the SOD-like activity of MnPs. It is further proportional to kred(ONOO–) and the ability of MnPs to prevent lipid peroxidation. In turn, the inhibition of lipid peroxidation by MnPs is also proportional to their SOD-like activity. In an in vivo S. cerevisiae assay, however, while E1/2 predominates, lipophilicity significantly affects the efficacy of MnPs. MnPs of similar log POW and E1/2, that have linear alkyl or alkoxyalkyl pyridyl substituents, distribute more easily within a cell and in turn provide higher protection to S. cerevisiae in comparison to MnP with bulky cyclic substituents. The bell-shape curve, with MnTE-2-PyP5+ exhibiting the highest ability to catalyze ascorbate oxidation, has been established and discussed. Our data support the notion that the SOD-like activity of MnPs parallels their therapeutic potential, though species other than O2•–, such as peroxynitrite, H2O2, lipid reactive species, and cellular reductants, may be involved in their mode(s) of action(s).

Izvorni jezik
Engleski

Znanstvena područja
Kemija



POVEZANOST RADA


Ustanove
Farmaceutsko-biokemijski fakultet, Zagreb

Profili:

Avatar Url Ines Batinić-Haberle (autor)

Avatar Url Tin Weitner (autor)

Citiraj ovu publikaciju

Tovmasyan, Artak; Carballal, Sebastian; Ghazaryan, Robert; Melikyan, Lida; Weitner, Tin; Maia, Clarissa G. C.; Reboucas, Julio S.; Radi, Rafael; Spasojević, Ivan; Benov, Ludmil et al.
Rational Design of Superoxide Dismutase (SOD) Mimics: The Evaluation of the Therapeutic Potential of New Cationic Mn Porphyrins with Linear and Cyclic Substituents // Inorganic chemistry, 53 (2014), 21; 11467-11483 doi:10.1021/ic501329p (međunarodna recenzija, članak, znanstveni)
Tovmasyan, A., Carballal, S., Ghazaryan, R., Melikyan, L., Weitner, T., Maia, C., Reboucas, J., Radi, R., Spasojević, I. & Benov, L. (2014) Rational Design of Superoxide Dismutase (SOD) Mimics: The Evaluation of the Therapeutic Potential of New Cationic Mn Porphyrins with Linear and Cyclic Substituents. Inorganic chemistry, 53 (21), 11467-11483 doi:10.1021/ic501329p.
@article{article, year = {2014}, pages = {11467-11483}, DOI = {10.1021/ic501329p}, keywords = {Mn porphyrins, redox properties, lipophilicity, therapeutic potential}, journal = {Inorganic chemistry}, doi = {10.1021/ic501329p}, volume = {53}, number = {21}, issn = {0020-1669}, title = {Rational Design of Superoxide Dismutase (SOD) Mimics: The Evaluation of the Therapeutic Potential of New Cationic Mn Porphyrins with Linear and Cyclic Substituents}, keyword = {Mn porphyrins, redox properties, lipophilicity, therapeutic potential} }

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE


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