The effect of peroxynitrite decomposition catalyst MnTBAP on aldehyde dehydrogenase-2 nitration by organic nitrates: Role in nitrate tolerance

Vincenzo Mollace, Carolina Muscoli, Concetta Dagostino, Luigino Antonio Giancotti, Micaela Gliozzi, Iolanda Sacco, Valeria Visalli, Santo Gratteri, Ernesto Palma, Natalia Malara, Vincenzo Musolino, Cristina Carresi, Saverio Muscoli, Cristiana Vitale, Daniela Salvemini, Francesco Romeo

Research output: Contribution to journalArticle

7 Citations (Scopus)

Abstract

Bioconversion of glyceryl trinitrate (GTN) into nitric oxide (NO) by aldehyde dehydrogenase-2 (ALDH-2) is a crucial mechanism which drives vasodilatory and antiplatelet effect of organic nitrates in vitro and in vivo. Oxidative stress generated by overproduction of free radical species, mostly superoxide anions and NO-derived peroxynitrite, has been suggested to play a pivotal role in the development of nitrate tolerance, though the mechanism still remains unclear. Here we studied the free radical-dependent impairment of ALDH-2 in platelets as well as vascular tissues undergoing organic nitrate ester tolerance and potential benefit when using the selective peroxynitrite decomposition catalyst Mn(III) tetrakis (4-Benzoic acid) porphyrin (MnTBAP). Washed human platelets were made tolerant to nitrates via incubation with GTN for 4 h. This was expressed by attenuation of platelet aggregation induced by thrombin (40 U/mL), an effect accompanied by GTN-related induction of cGMP levels in platelets undergoing thrombin-induced aggregation. Both effects were associated to attenuated GTN-induced nitrite formation in platelets supernatants and to prominent nitration of ALDH-2, the GTN to NO metabolizing enzyme, suggesting that GTN tolerance was associated to reduced NO formation via impairment of ALDH-2. These effects were all antagonized by co-incubation of platelets with MnTBAP, which restored GTN-induced responses in tolerant platelets. Comparable effect was found under in in vivo settings. Indeed, MnTBAP (10 mg/kg, i.p.) significantly restored the hypotensive effect of bolus injection of GTN in rats made tolerants to organic nitrates via chronic administration of isosorbide-5-mononitrate (IS-5-MN), thus confirming the role of peroxynitrite overproduction in the development of tolerance to vascular responses induced by organic nitrates. In conclusion, oxidative stress subsequent to prolonged use of organic nitrates, which occurs via nitration of ALDH-2, represents a key event in GTN tolerance, an effect counteracted both in vitro and in vivo by novel peroxynitrite decomposition catalyst.

Original languageEnglish
Pages (from-to)29-35
Number of pages7
JournalPharmacological Research
Volume89
DOIs
Publication statusPublished - 2014

Fingerprint

Aldehyde Dehydrogenase
Peroxynitrous Acid
Nitroglycerin
Nitrates
Blood Platelets
Nitric Oxide
isosorbide-5-mononitrate
Thrombin
Free Radicals
Blood Vessels
Oxidative Stress
manganese(III)-tetrakis(4-benzoic acid)porphyrin
Nitrites
Platelet Aggregation
Superoxides
Esters
Injections

Keywords

  • Nitrate tolerance Oxidative stress ALDH-2 nitration Peroxynitrite decomposition catalyst

ASJC Scopus subject areas

  • Pharmacology
  • Medicine(all)

Cite this

The effect of peroxynitrite decomposition catalyst MnTBAP on aldehyde dehydrogenase-2 nitration by organic nitrates : Role in nitrate tolerance. / Mollace, Vincenzo; Muscoli, Carolina; Dagostino, Concetta; Giancotti, Luigino Antonio; Gliozzi, Micaela; Sacco, Iolanda; Visalli, Valeria; Gratteri, Santo; Palma, Ernesto; Malara, Natalia; Musolino, Vincenzo; Carresi, Cristina; Muscoli, Saverio; Vitale, Cristiana; Salvemini, Daniela; Romeo, Francesco.

In: Pharmacological Research, Vol. 89, 2014, p. 29-35.

Research output: Contribution to journalArticle

Mollace, V, Muscoli, C, Dagostino, C, Giancotti, LA, Gliozzi, M, Sacco, I, Visalli, V, Gratteri, S, Palma, E, Malara, N, Musolino, V, Carresi, C, Muscoli, S, Vitale, C, Salvemini, D & Romeo, F 2014, 'The effect of peroxynitrite decomposition catalyst MnTBAP on aldehyde dehydrogenase-2 nitration by organic nitrates: Role in nitrate tolerance', Pharmacological Research, vol. 89, pp. 29-35. https://doi.org/10.1016/j.phrs.2014.07.007
Mollace, Vincenzo ; Muscoli, Carolina ; Dagostino, Concetta ; Giancotti, Luigino Antonio ; Gliozzi, Micaela ; Sacco, Iolanda ; Visalli, Valeria ; Gratteri, Santo ; Palma, Ernesto ; Malara, Natalia ; Musolino, Vincenzo ; Carresi, Cristina ; Muscoli, Saverio ; Vitale, Cristiana ; Salvemini, Daniela ; Romeo, Francesco. / The effect of peroxynitrite decomposition catalyst MnTBAP on aldehyde dehydrogenase-2 nitration by organic nitrates : Role in nitrate tolerance. In: Pharmacological Research. 2014 ; Vol. 89. pp. 29-35.
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AU - Dagostino, Concetta

AU - Giancotti, Luigino Antonio

AU - Gliozzi, Micaela

AU - Sacco, Iolanda

AU - Visalli, Valeria

AU - Gratteri, Santo

AU - Palma, Ernesto

AU - Malara, Natalia

AU - Musolino, Vincenzo

AU - Carresi, Cristina

AU - Muscoli, Saverio

AU - Vitale, Cristiana

AU - Salvemini, Daniela

AU - Romeo, Francesco

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N2 - Bioconversion of glyceryl trinitrate (GTN) into nitric oxide (NO) by aldehyde dehydrogenase-2 (ALDH-2) is a crucial mechanism which drives vasodilatory and antiplatelet effect of organic nitrates in vitro and in vivo. Oxidative stress generated by overproduction of free radical species, mostly superoxide anions and NO-derived peroxynitrite, has been suggested to play a pivotal role in the development of nitrate tolerance, though the mechanism still remains unclear. Here we studied the free radical-dependent impairment of ALDH-2 in platelets as well as vascular tissues undergoing organic nitrate ester tolerance and potential benefit when using the selective peroxynitrite decomposition catalyst Mn(III) tetrakis (4-Benzoic acid) porphyrin (MnTBAP). Washed human platelets were made tolerant to nitrates via incubation with GTN for 4 h. This was expressed by attenuation of platelet aggregation induced by thrombin (40 U/mL), an effect accompanied by GTN-related induction of cGMP levels in platelets undergoing thrombin-induced aggregation. Both effects were associated to attenuated GTN-induced nitrite formation in platelets supernatants and to prominent nitration of ALDH-2, the GTN to NO metabolizing enzyme, suggesting that GTN tolerance was associated to reduced NO formation via impairment of ALDH-2. These effects were all antagonized by co-incubation of platelets with MnTBAP, which restored GTN-induced responses in tolerant platelets. Comparable effect was found under in in vivo settings. Indeed, MnTBAP (10 mg/kg, i.p.) significantly restored the hypotensive effect of bolus injection of GTN in rats made tolerants to organic nitrates via chronic administration of isosorbide-5-mononitrate (IS-5-MN), thus confirming the role of peroxynitrite overproduction in the development of tolerance to vascular responses induced by organic nitrates. In conclusion, oxidative stress subsequent to prolonged use of organic nitrates, which occurs via nitration of ALDH-2, represents a key event in GTN tolerance, an effect counteracted both in vitro and in vivo by novel peroxynitrite decomposition catalyst.

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