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1.
Parasitol Int ; 73: 101948, 2019 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-31247308

RESUMO

This study aimed to evaluate nucleoside triphosphate diphosphohydrolase (NTPDase) and adenosine deaminase (ADA) activities in lymphocytes from rats supplemented or not with curcumin 30 days prior to experimental infection with Trypanosoma evansi. Thirty-two adult male Wistar rats were divided in four groups. The pre-infection group 20 (PreI20) received orally 20 mg/kg of curcumin and pre-infection group 60 (PreI60) received orally 60 mg/kg of curcumin for 30 days prior inoculation with T. evansi. The infected e non-infected control groups received only oral vehicle for 30 days. Trypanosoma evansi infected groups were inoculated intraperitoneally with 0.2 ml of blood with 1 × 106 parasites. After inoculation the treatment of the groups continued until the day of euthanasia (15 days). The results showed that curcumin pre-treatment, with both doses, reduced (P < .05) NTPDase and increased (P < .05) ADA activity in lymphocytes of treated groups when compared to untreated and infected animals (control). The results of this study support the evidence that the regulation of ATP and adenosine levels by NTPDase and ADA activities appear to be important to modulate the immune response in T. evansi infection, once the treatment with curcumin maintained the NTPDase activity reduced and enhanced ADA activity in lymphocytes. It is possible to conclude that the use of curcumin prior to infection with T. evansi induces immunomodulatory effects, favoring the response against the parasite.


Assuntos
Nucleotídeos de Adenina/metabolismo , Adenosina Trifosfatases/metabolismo , Curcumina/metabolismo , Imunomodulação/efeitos dos fármacos , Tripanossomíase/metabolismo , Ração Animal/análise , Animais , Curcumina/administração & dosagem , Dieta/veterinária , Suplementos Nutricionais/análise , Relação Dose-Resposta a Droga , Linfócitos/parasitologia , Masculino , Distribuição Aleatória , Ratos , Ratos Wistar , Trypanosoma/fisiologia
2.
Mol Cell Biochem ; 386(1-2): 199-210, 2014 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-24130039

RESUMO

This study evaluated the effects of curcumin and/or insulin on antioxidant enzyme activity in blood, liver, and kidney, as well as on lipid peroxidation and delta aminolevulinic dehydratase (δ-ALA-D) activity, and a histopathological analysis of streptozotocin-induced diabetic rats. The animals were divided into six groups (n = 6): control/saline (C); control/curcumin (CCur); diabetic/saline (D); diabetic/insulin (DIns); diabetic/curcumin (DCur); and diabetic/insulin/curcumin (DInsCur). After 30 days of treatment with curcumin and/or insulin, the animals were sacrificed and the liver, kidney, and serum were used for experimental determinations. Results of histopathological analysis showed that the treatment with insulin ameliorate renal and hepatic lesions from both DIns and DInsCur groups. TBARS levels were significantly increased in serum, liver, and kidney in D group and the administration of curcumin and insulin prevented this increase in DIns and DCur groups. The activities of catalase (CAT), superoxide dismutase, and δ-ALA-D presented a significant decrease in the liver and kidney D group when compared to C group (P < 0.05). The animals treated with curcumin and insulin presented an increase of CAT activity, revealing a positive interaction between both substances. The treatments with curcumin or insulin prevented oxidative stress in blood, through modulation of enzymatic antioxidant defenses. These findings contributed to the comprehension that antioxidants from medicinal plants could be used as adjuvant in the treatment of this endocrinopathy and not as single therapy.


Assuntos
Curcumina/administração & dosagem , Diabetes Mellitus Experimental/metabolismo , Insulina/administração & dosagem , Rim/metabolismo , Fígado/metabolismo , Estresse Oxidativo , Animais , Glicemia/análise , Peso Corporal , Catalase/sangue , Diabetes Mellitus Experimental/sangue , Rim/enzimologia , Peroxidação de Lipídeos , Fígado/enzimologia , Masculino , Sintase do Porfobilinogênio/metabolismo , Ratos , Ratos Wistar , Estreptozocina , Superóxido Dismutase/metabolismo
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