Repositioning of leishmanicidal [1,2,3]Triazolo[1,5-a]pyridinium salts for Chagas disease treatment: Trypanosoma cruzi cell death involving mitochondrial membrane depolarisation and Fe-SOD inhibition
Abstract Trypanosomatidae is a family of unicellular parasites belonging to the phylum Euglenozoa, which are causative agents in high impact human diseases such as Leishmaniasis, Chagas disease and African sleeping sickness. The impact on human health and local economies, together with a lack of satisfactory chemotherapeutic treatments and effective vaccines, justifies stringent research efforts to search for new disease therapies. Here, we present in vitro trypanocidal activity data and mode of action data, repositioning leishmanicidal [1,2,3]Triazolo[1,5-a]pyridinium salts against Trypanosoma cruzi, the aetiological agent of Chagas disease. This disease is one of the most neglected tropical diseases and is a major public health issue in Central and South America. The disease affects approximately 6–7 million people and is widespread due to increased migratory movements. We screened a suite of leishmanicidal [1,2,3]Triazolo[1,5-a]pyridinium salt compounds, of which compounds 13, 20 and 21 were identified as trypanocidal drugs. These compounds caused cell death in a mitochondrion-dependent manner through a bioenergetic collapse. Moreover, compounds 13 and 20 showed a remarkable inhibition of iron superoxide dismutase activity of T. cruzi, a key enzyme in the protection from the damage produced by oxidative stress..
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2020 |
---|---|
Erschienen: |
2020 |
Enthalten in: |
Zur Gesamtaufnahme - volume:119 |
---|---|
Enthalten in: |
Parasitology research - 119(2020), 9 vom: 01. Juli, Seite 2943-2954 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Martín-Escolano, Rubén [VerfasserIn] |
---|
Links: |
Volltext [lizenzpflichtig] |
---|
BKL: | |
---|---|
Themen: |
Chagas disease |
doi: |
10.1007/s00436-020-06779-0 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
SPR040678164 |
---|
LEADER | 01000caa a22002652 4500 | ||
---|---|---|---|
001 | SPR040678164 | ||
003 | DE-627 | ||
005 | 20230519111209.0 | ||
007 | cr uuu---uuuuu | ||
008 | 201007s2020 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1007/s00436-020-06779-0 |2 doi | |
035 | |a (DE-627)SPR040678164 | ||
035 | |a (SPR)s00436-020-06779-0-e | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
082 | 0 | 4 | |a 590 |a 610 |q ASE |
084 | |a 44.44 |2 bkl | ||
084 | |a 42.00 |2 bkl | ||
100 | 1 | |a Martín-Escolano, Rubén |e verfasserin |4 aut | |
245 | 1 | 0 | |a Repositioning of leishmanicidal [1,2,3]Triazolo[1,5-a]pyridinium salts for Chagas disease treatment: Trypanosoma cruzi cell death involving mitochondrial membrane depolarisation and Fe-SOD inhibition |
264 | 1 | |c 2020 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a Computermedien |b c |2 rdamedia | ||
338 | |a Online-Ressource |b cr |2 rdacarrier | ||
520 | |a Abstract Trypanosomatidae is a family of unicellular parasites belonging to the phylum Euglenozoa, which are causative agents in high impact human diseases such as Leishmaniasis, Chagas disease and African sleeping sickness. The impact on human health and local economies, together with a lack of satisfactory chemotherapeutic treatments and effective vaccines, justifies stringent research efforts to search for new disease therapies. Here, we present in vitro trypanocidal activity data and mode of action data, repositioning leishmanicidal [1,2,3]Triazolo[1,5-a]pyridinium salts against Trypanosoma cruzi, the aetiological agent of Chagas disease. This disease is one of the most neglected tropical diseases and is a major public health issue in Central and South America. The disease affects approximately 6–7 million people and is widespread due to increased migratory movements. We screened a suite of leishmanicidal [1,2,3]Triazolo[1,5-a]pyridinium salt compounds, of which compounds 13, 20 and 21 were identified as trypanocidal drugs. These compounds caused cell death in a mitochondrion-dependent manner through a bioenergetic collapse. Moreover, compounds 13 and 20 showed a remarkable inhibition of iron superoxide dismutase activity of T. cruzi, a key enzyme in the protection from the damage produced by oxidative stress. | ||
650 | 4 | |a Chagas disease |7 (dpeaa)DE-He213 | |
650 | 4 | |a Chemotherapy |7 (dpeaa)DE-He213 | |
650 | 4 | |a Pyridines |7 (dpeaa)DE-He213 | |
650 | 4 | |a Superoxide dismutase |7 (dpeaa)DE-He213 | |
650 | 4 | |a Trypanocidal agents |7 (dpeaa)DE-He213 | |
700 | 1 | |a Martín-Escolano, Javier |e verfasserin |4 aut | |
700 | 1 | |a Ballesteros-Garrido, Rafael |e verfasserin |4 aut | |
700 | 1 | |a Cirauqui, Nuria |e verfasserin |4 aut | |
700 | 1 | |a Abarca, Belén |e verfasserin |4 aut | |
700 | 1 | |a Rosales, María José |e verfasserin |4 aut | |
700 | 1 | |a Sánchez-Moreno, Manuel |e verfasserin |4 aut | |
700 | 1 | |a Ballesteros, Rafael |e verfasserin |4 aut | |
700 | 1 | |a Marín, Clotilde |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Parasitology research |d Berlin : Springer, 1928 |g 119(2020), 9 vom: 01. Juli, Seite 2943-2954 |w (DE-627)SPR005883253 |w (DE-600)1462976-8 |x 1432-1955 |7 nnns |
773 | 1 | 8 | |g volume:119 |g year:2020 |g number:9 |g day:01 |g month:07 |g pages:2943-2954 |
856 | 4 | 0 | |u https://dx.doi.org/10.1007/s00436-020-06779-0 |z lizenzpflichtig |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_SPRINGER | ||
912 | |a SSG-OLC-PHA | ||
936 | b | k | |a 44.44 |q ASE |
936 | b | k | |a 42.00 |q ASE |
951 | |a AR | ||
952 | |d 119 |j 2020 |e 9 |b 01 |c 07 |h 2943-2954 |