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1.
Neurosci Lett ; 709: 134378, 2019 09 14.
Article in English | MEDLINE | ID: mdl-31325582

ABSTRACT

Oxaliplatin is a third-generation platinum drug commonly used as the first line treatment of metastatic colorectal cancer. Oxaliplatin-based anticancer regimens course with dose-limiting neurotoxicity. The pharmacological strategies used to manage such side effect are not totally effective. Metformin is an anti-diabetic drug that is described to negatively modulate painful diabetic neuropathy. Then, this study aimed to assess the effect of metformin in the oxaliplatin-induced peripheral sensory neuropathy in mice. For that purpose, Swiss male mice were injected with oxaliplatin (1, 2 or 4 mg/kg, i.v., twice a week with a total of nine injections) alone or in combination with daily administration of metformin (250 mg/kg, p.o.). Thermal and mechanical nociceptive tests were performed once a week for five weeks. Then, the animals were euthanized on day 35 post-first injection of oxaliplatin and the dorsal root ganglia were harvested for the assessment of c-Fos and ATF3 expressions. Oxaliplatin caused a nociceptive response accompanied by the increased expression of c-Fos and ATF3 in the dorsal root ganglia and spinal cord. In addition, the oxaliplatin-associated nociception was significantly attenuated by metformin (P < 0.05), which also reduced the expression of c-Fos and ATF3 (P < 0.05). Therefore, metformin protected from the peripheral sensory neuropathy induced by oxaliplatin, which was confirmed by the reduction of c-Fos and ATF3 expression, two known neuronal activation and damage markers, respectively.


Subject(s)
Activating Transcription Factor 3/antagonists & inhibitors , Ganglia, Spinal/metabolism , Metformin/therapeutic use , Oxaliplatin/toxicity , Peripheral Nervous System Diseases/metabolism , Proto-Oncogene Proteins c-fos/antagonists & inhibitors , Activating Transcription Factor 3/biosynthesis , Activating Transcription Factor 3/genetics , Animals , Antineoplastic Agents/toxicity , Ganglia, Spinal/drug effects , Gene Expression , Hypoglycemic Agents/pharmacology , Hypoglycemic Agents/therapeutic use , Male , Metformin/pharmacology , Mice , Peripheral Nervous System Diseases/drug therapy , Peripheral Nervous System Diseases/genetics , Proto-Oncogene Proteins c-fos/biosynthesis , Proto-Oncogene Proteins c-fos/genetics
2.
Int Immunopharmacol ; 62: 96-108, 2018 Sep.
Article in English | MEDLINE | ID: mdl-29990699

ABSTRACT

Ifosfamide (IFO) is an antineoplastic drug that is commonly used to treat gynecological and breast cancers. Hemorrhagic cystitis (HC) is a common side effect associated with IFO injection, which courses with neutrophil accumulation and affects 6-50% of patients depending on dose intensity. Here, we investigated the role of neutrophils in this inflammatory process. Female Swiss mice (n = 8/group) were injected with saline, IFO (400 mg/kg, i.p.), fucoidan (a P- and L-selectins inhibitor, 100 mg/kg, i.v.) or IFO + fucoidan (1-100 mg/kg) alone or combined with mesna (80 mg/kg i.p.). Another group of mice received anti-Ly6G antibody (500 µg/mouse, once daily for 2 days) for neutrophil depletion before IFO injection. In another experimental setting, animals received granulocyte colony-stimulating factor (G-CSF, 400 µg/kg), IFO (200 mg/kg), G-CSF (25-400 µg/kg, for 5 days) + IFO (200 mg/kg, i.p.) or fucoidan + G-CSF + IFO. Bladder injury was evaluated 12 h after IFO injection. IFO 400 mg/kg significantly increased visceral hyperalgesia, bladder edema, hemorrhage, vascular permeability, MPO, IL-1ß and IL-6 tissue levels, and COX-2 immunostaining and expression versus the saline group (P < 0.05). Conversely, fucoidan (100 mg/kg) significantly attenuated these parameters compared to IFO-injected mice (P < 0.05). Additionally, fucoidan potentiated mesna protective effect when compared with IFO + mesna group (P < 0.05). Accordingly, neutrophil depletion with anti-Ly6G reduced inflammatory parameters and bladder injury compared to IFO (P < 0.05). In contrast, G-CSF enhanced IFO (200 mg/kg)-induced HC, which was significantly attenuated by treatment with fucoidan (P < 0.05). Therefore, neutrophils contribute to the pathogenesis of HC.


Subject(s)
Antineoplastic Agents, Alkylating/adverse effects , Cystitis/chemically induced , Hemorrhage/chemically induced , Ifosfamide/adverse effects , Neutrophil Infiltration/drug effects , Protective Agents/therapeutic use , Animals , Cystitis/immunology , Cystitis/pathology , Cystitis/prevention & control , Drug Therapy, Combination , Female , Hemorrhage/immunology , Hemorrhage/pathology , Hemorrhage/prevention & control , Mesna/administration & dosage , Mesna/therapeutic use , Mice , Polysaccharides/administration & dosage , Polysaccharides/therapeutic use , Protective Agents/administration & dosage
3.
Acta Cir Bras ; 29(12): 787-93, 2014 Dec.
Article in English | MEDLINE | ID: mdl-25517491

ABSTRACT

PURPOSE: To study the anti-inflammatory actions of electroacupuncture (EAc) on an experimental colitis model in mice. METHODS: Thirty-eight male Swiss mice, divided in five groups, were subjected to induction of colitis by TNBS in 50% ethanol. Saline (SAL) and ethanol (ETNL) groups served as controls. TNBS+EAc and TNBS+ dexamethasone subgroups were treated with EAc 100Hz and dexamethasone (DEXA) 1 mg/Kg/day, respectively. After three days, a colon segment was obtained for quantification of myeloperoxidase (MPO) activity, immunohistochemistry for iNOS, malondialdehyde (MDA) and cytokines (IL-1ß and IL-10). RESULTS: Neutrophilic activity, assayed as MPO activity, was significantly higher in the TNBS colitis group than that in the saline control group. TNBS+EAc group showed suppression of IL-10 in the colon. EAc treatment significantly reduced the concentration of MDA and the expression of iNOS, as compared to the other groups. CONCLUSION: Electroacupuncture 100Hz applied to acupoint ST-36 promotes an anti-inflammatory action on the TNBS-induced colitis, mediated by increase of IL-10 and decrease of iNOS expression.


Subject(s)
Anti-Inflammatory Agents/therapeutic use , Colitis/therapy , Electroacupuncture/methods , Interleukin-10/metabolism , Nitric Oxide Synthase Type II/metabolism , Peroxidase/metabolism , Acupuncture Points , Animals , Colitis/chemically induced , Colon/metabolism , Disease Models, Animal , Immunohistochemistry , Inflammatory Bowel Diseases/drug therapy , Inflammatory Bowel Diseases/therapy , Interleukin-1beta/metabolism , Male , Malondialdehyde/metabolism , Mice , Nitric Oxide Synthase Type II/antagonists & inhibitors , Random Allocation , Trinitrobenzenesulfonic Acid
4.
Acta cir. bras ; 29(12): 787-793, 12/2014. tab, graf
Article in English | LILACS | ID: lil-731031

ABSTRACT

PURPOSE: To study the anti-inflammatory actions of electroacupuncture (EAc) on an experimental colitis model in mice. METHODS: Thirty-eight male Swiss mice, divided in five groups, were subjected to induction of colitis by TNBS in 50% ethanol. Saline (SAL) and ethanol (ETNL) groups served as controls. TNBS+EAc and TNBS+ dexamethasone subgroups were treated with EAc 100Hz and dexamethasone (DEXA) 1 mg/Kg/day, respectively. After three days, a colon segment was obtained for quantification of myeloperoxidase (MPO) activity, immunohistochemistry for iNOS, malondialdehyde (MDA) and cytokines (IL-1β and IL-10). RESULTS: Neutrophilic activity, assayed as MPO activity, was significantly higher in the TNBS colitis group than that in the saline control group. TNBS+EAc group showed suppression of IL-10 in the colon. EAc treatment significantly reduced the concentration of MDA and the expression of iNOS, as compared to the other groups. CONCLUSION: Electroacupuncture 100Hz applied to acupoint ST-36 promotes an anti-inflammatory action on the TNBS-induced colitis, mediated by increase of IL-10 and decrease of iNOS expression. .


Subject(s)
Animals , Male , Mice , Anti-Inflammatory Agents/therapeutic use , Colitis/therapy , Electroacupuncture/methods , /metabolism , Nitric Oxide Synthase Type II/metabolism , Peroxidase/metabolism , Acupuncture Points , Colitis/chemically induced , Colon/metabolism , Disease Models, Animal , Immunohistochemistry , Inflammatory Bowel Diseases/drug therapy , Inflammatory Bowel Diseases/therapy , Interleukin-1beta/metabolism , Malondialdehyde/metabolism , Nitric Oxide Synthase Type II/antagonists & inhibitors , Random Allocation , Trinitrobenzenesulfonic Acid
5.
Acta cir. bras ; 29(12): 1-7, 12/2014. graf, tab, ilus
Article in English | LILACS, VETINDEX | ID: biblio-1456222

ABSTRACT

PURPOSE:To study the anti-inflammatory actions of electroacupuncture (EAc) on an experimental colitis model in mice.METHODS:Thirty-eight male Swiss mice, divided in five groups, were subjected to induction of colitis by TNBS in 50% ethanol. Saline (SAL) and ethanol (ETNL) groups served as controls. TNBS+EAc and TNBS+ dexamethasone subgroups were treated with EAc 100Hz and dexamethasone (DEXA) 1 mg/Kg/day, respectively. After three days, a colon segment was obtained for quantification of myeloperoxidase (MPO) activity, immunohistochemistry for iNOS, malondialdehyde (MDA) and cytokines (IL-1β and IL-10).RESULTS:Neutrophilic activity, assayed as MPO activity, was significantly higher in the TNBS colitis group than that in the saline control group. TNBS+EAc group showed suppression of IL-10 in the colon. EAc treatment significantly reduced the concentration of MDA and the expression of iNOS, as compared to the other groups. CONCLUSION: Electroacupuncture 100Hz applied to acupoint ST-36 promotes an anti-inflammatory action on the TNBS-induced colitis, mediated by increase of IL-10 and decrease of iNOS expression.


Subject(s)
Animals , Mice , Colitis/chemically induced , Electroacupuncture/veterinary , Trinitrobenzenes , Nitric Oxide Synthase
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