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1.
Parasitology ; 145(8): 1059-1064, 2018 07.
Article in English | MEDLINE | ID: mdl-29208061

ABSTRACT

Cathelicidins are antimicrobial peptides produced by humans and animals in response to various pathogenic microbes. Crotalicidin (Ctn), a cathelicidin-related vipericidin from the South American Crotalus durissus terrificus rattlesnake's venom gland, and its fragments have demonstrated antimicrobial and antifungal activity, similarly to human cathelicidin LL-37. In order to provide templates for the development of modern trypanocidal agents, the present study evaluated the antichagasic effect of these four peptides (Ctn, Ctn[1-14], Ctn[15-34] and LL-37). Herein, Ctn and short derived peptides were tested against the epimastigote, trypomastigote and amastigote forms of Trypanosoma cruzi Y strain (benznidazole-resistant strain) and cytotoxicity in mammalian cells was evaluated against LLC-MK2 lineage cells. Ctn inhibited all T. cruzi developmental forms, including amastigotes, which is implicated in the burden of infection in the chronic phase of Chagas disease. Moreover, Ctn showed a high selective index against trypomastigote forms (>200). Ctn induced cell death in T. cruzi through necrosis, as determined by flow cytometry analyses with specific molecular probes and morphological alterations, such as loss of membrane integrity and cell shrinkage, as observed through scanning electron microscopy. Overall, Ctn seems to be a promising template for the development of antichagasic agents.


Subject(s)
Peptide Fragments/pharmacology , Trypanocidal Agents/pharmacology , Trypanosoma cruzi/drug effects , Animals , Antimicrobial Cationic Peptides/pharmacology , Cell Line , Cell Survival/drug effects , Crotalid Venoms/pharmacology , Flow Cytometry , Haplorhini , Inhibitory Concentration 50 , Microscopy, Electron, Scanning , Trypanosoma cruzi/ultrastructure , Cathelicidins
2.
Toxicon ; 61: 38-46, 2013 Jan.
Article in English | MEDLINE | ID: mdl-23127898

ABSTRACT

Bites from snake (Bothrops genus) cause local tissue damage and systemic complications, which include alterations such as hemostatic system and acute renal failure (ARF). Recent studies suggest that ARF pathogenesis in snakebite envenomation is multifactorial and involves hemodynamic disturbances, immunologic reactions and direct nephrotoxicity. The aim of the work was to investigate the effects of the Bothrops leucurus venom (BlV) in the renal perfusion system and in cultured renal tubular cells of the type MDCK (Madin-Darby Canine kidney). BlV (10 µg/mL) reduced the perfusion pressure at 90 and 120 min. The renal vascular resistance (RVR) decreased at 120 min of perfusion. The effect on urinary flow (UF) and glomerular filtration rate (GFR) started 30 min after BlV infusion, was transient and returned to normal at 120 min of perfusion. It was also observed a decrease on percentual tubular transport of sodium (%TNa(+)) at 120 min and of chloride (%TCl(-)) at 60 and 90 min. The treatment with BlV caused decrease in cell viability to the lowest concentration tested with an IC(50) of 1.25 µg/mL. Flow cytometry with annexin V and propidium iodide showed that cell death occurred predominantly by necrosis. However, a cell death process may involve apoptosis in lower concentrations. BlV treatment (1.25 µg/mL) led to significant depolarization of the mitochondrial membrane potential and, indeed, we found an increase in the expression of cell death genes in the lower concentrations tested. The venom also evoked an increase in the cytosolic Ca(2+) in a concentration dependent manner, indicating that Ca(2+) may participate in the venom of B. leucurus effect. The characterization of the effects in the isolated kidney and renal tubular cells gives strong evidences that the acute renal failure induced by this venom is a result of the direct nephrotoxicity which may involve the cell death mechanism.


Subject(s)
Bothrops , Crotalid Venoms/toxicity , Epithelium/pathology , Kidney Diseases/chemically induced , Kidney Diseases/pathology , Kidney Tubules/pathology , Animals , Annexin A5 , Apoptosis Regulatory Proteins/biosynthesis , Apoptosis Regulatory Proteins/genetics , Calcium/metabolism , Cell Survival/drug effects , Cells, Cultured , Coloring Agents , Dogs , Epithelial Cells/drug effects , Epithelial Cells/pathology , Epithelium/drug effects , Fluorescein-5-isothiocyanate , Fluorescent Dyes , Gene Expression/drug effects , Kidney Tubules/drug effects , Male , Organ Culture Techniques , Propidium , Rats
3.
Nat Prod Commun ; 5(7): 1103-6, 2010 Jul.
Article in English | MEDLINE | ID: mdl-20734950

ABSTRACT

The effect was investigated of the K+ channel blocker, glibenclamide, on the ability of Crotalus durissus cumanensis venom (CDCM) to promote peripheral antinociception. This was measured by formalin-induced nociception in male Swiss mice. CDCM (200 and 300 microg/kg) produced an antinociceptive effect during phase 2 in the formalin test. The effect of CDCM (200 microg/kg) was unaffected by the ATP-sensitive K+ channel blocker glibenclamide (2 mg/kg). These results suggest that CDCM is effective against acute pain. However, the ATP-sensitive K+ channels pathway is not contributable to the antinociceptive mechanism of CDCM.


Subject(s)
Analgesics/therapeutic use , Crotalus/metabolism , KATP Channels/metabolism , Pain/drug therapy , Pain/metabolism , Snake Venoms/therapeutic use , Animals , Glyburide/pharmacology , KATP Channels/antagonists & inhibitors , Male , Mice , Potassium Channel Blockers/pharmacology
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