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Toxicol Appl Pharmacol ; 418: 115497, 2021 05 01.
Article in English | MEDLINE | ID: mdl-33744277

ABSTRACT

Medical reports indicate a prevalence of pain in 50% of patients with cancer. In this context, this article investigated the antinociceptive activity of α-PHE using in vivo Sarcoma-180-induced hypernociception in mice to detail its mechanism(s) of antinociception under different conditions of treatment and tumor progression. Firsty, in vitro cytotoxic action was assessed using melanoma B-16/F-10 and S-180 murine cells and colorimetric MTT assays. For in vivo studies, acute treatment with α-PHE (6.25, 12.5, 25 and 50 mg/kg orally by gavage) was performed on the 1st day after S-180 inoculation. Subacute treatments were performed for 8 days starting on the next day (early protocol) or on day 8 after S-180 inoculation (late protocol). For all procedures, mechanical nociceptive evaluations were carried out by von Frey's technique in the subaxillary region peritumoral tissue (direct nociception) and in right legs of S-180-bearing mice (indirect nociception). α-PHE showed in vitro cytotoxic action on B-16/F-10 and S-180 (CI50 values of 436.0 and 217.9 µg/mL), inhibition of in vivo tumor growth (ranging from 47.3 to 82.7%) and decreased direct (peritumoral tissue in subaxillary region) and indirect (right leg) mechanical nociception in Sarcoma 180-bearing mice with early and advanced tumors under acute or subacute conditions of treatment especially at doses of 25 and 50 mg/kg. It improved serum levels of GSH as well as diminished systemic lipid peroxidation, blood cytokines (interleukin-1ß, -4, -6, and tumor necrosis factor-α). Such outcomes highlight α-PHE as a promising lead compound that combines antinociceptive and antineoplasic properties. Its structural simplicity make it a cost-effective alternative, justifying further mechanistic investigations and the development of pharmaceutical formulations. Moreover, the protocols developed and standardized here make it possible to use Sarcoma-180 hypernociception model to evaluate the capacity of new antinociceptive molecules under conditions of cancer-related allodynia.


Subject(s)
Analgesics/pharmacology , Antineoplastic Agents/pharmacology , Cancer Pain/drug therapy , Cyclohexane Monoterpenes/pharmacology , Melanoma, Experimental/drug therapy , Sarcoma 180/drug therapy , Animals , Cancer Pain/etiology , Cancer Pain/metabolism , Cell Line, Tumor , Cell Proliferation/drug effects , Cytokines/metabolism , Female , Glutathione/metabolism , Inflammation Mediators/metabolism , Lipid Peroxidation/drug effects , Melanoma, Experimental/metabolism , Melanoma, Experimental/pathology , Mice , Pain Threshold , Sarcoma 180/complications , Sarcoma 180/metabolism , Sarcoma 180/pathology , Tumor Burden/drug effects , Tumor Cells, Cultured
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