Publications by authors named "Jose F Sarmento-Neto"

The current chemotherapy for cutaneous leishmaniasis (CL) is accompanied by side effects and drug resistance emergence, encouraging the proposal of new treatment approaches for this disease. ZnTnHex-2-PyP (ZnP hexyl) is a water-soluble Zn(II) porphyrin that exhibits remarkable potential for photodynamic therapy (PDT). This study aimed to investigate the ZnP hexyl-PDT against CL in vivo.

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Oxidative stress (OS) and endoplasmic reticulum stress (ERS) are at the genesis of placental disorders observed in preeclampsia, intrauterine growth restriction, and maternal hypothyroidism. In this regard, cationic manganese porphyrins (MnPs) comprise potent redox-active therapeutics of high antioxidant and anti-inflammatory potential, which have not been evaluated in metabolic gestational diseases yet. This study evaluated the therapeutic potential of two MnPs, [MnTE-2-PyP] (MnP I) and [MnT(5-Br-3-E-Py)P]5+ (MnP II), in the fetal-placental dysfunction of hypothyroid rats.

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Background: Photodynamic inactivation (PDI) is an attractive alternative to treat infections, especially considering the spread of resistant strains. The combination of the photophysical advantages of Zn(II) porphyrins (ZnPs) and the plasmonic effect of silver nanoparticles (AgNPs) has the potential to further improve PDI. Here, we propose the novel association of polyvinylpyrrolidone (PVP) coated AgNPs with the cationic ZnPs Zn(II) -tetrakis(-ethylpyridinium-2-yl)porphyrin or Zn(II) -tetrakis(-n-hexylpyridinium-2-yl)porphyrin to photoinactivate .

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is the main cause of superficial candidiasis. While the antifungals available are defied by biofilm formation and resistance emergence, antimicrobial photodynamic inactivation (aPDI) arises as an alternative antifungal therapy. The tetracationic metalloporphyrin Zn(II) -tetrakis(-n-hexylpyridinium-2-yl)porphyrin (ZnTnHex-2-PyP) has high photoefficiency and improved cellular interactions.

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Article Synopsis
  • - Photodynamic inactivation (PDI) using ZnTnHex-2-PyP, a potent photosensitizer, shows promise as a safer alternative for treating cutaneous leishmaniasis (CL), especially given the adverse effects and drug resistance seen with current chemotherapy options.
  • - The study demonstrated that ZnTnHex-2-PyP can inactivate over 95% of Leishmania promastigotes at low concentrations and significantly reduce parasite levels in infected macrophages, with minimal toxicity observed to mammalian cells.
  • - Findings suggest that ZnTnHex-2-PyP is stable and more effective than similar compounds, making it a strong candidate for future in vivo studies and potential applications against CL
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Background: Cardiomyopathies remain among the leading causes of death worldwide, despite all efforts and important advances in the development of cardiovascular therapeutics, demonstrating the need for new solutions. Herein, we describe the effects of the redox-active therapeutic Mn(III) -tetrakis(-ethylpyridinium-2-yl)porphyrin, AEOL10113, BMX-010 (MnTE-2-PyP), on rat heart as an entry to new strategies to circumvent cardiomyopathies.

Methods: Wistar rats weighing 250-300 g were used in both and experiments, to analyze intracellular Ca dynamics, L-type Ca currents, Ca spark frequency, intracellular reactive oxygen species (ROS) levels, and cardiomyocyte and cardiac contractility, in control and MnTE-2-PyP-treated cells, hearts, or animals.

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Pain is an unpleasant sensation associated with a wide range of injuries and diseases, and affects approximately 20% of adults in the world. The discovery of new and more effective drugs that can relieve pain is an important research goal in both the pharmaceutical industry and academia. This review describes studies involving antinociceptive activity of essential oils from 31 plant species.

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