Department of Microbiology and Parasitology, Universidade Federal de Santa Maria, Santa Maria, RS, Brazil.
Department of Physiology and Pharmacology, Universidade Federal de Santa Maria, Santa Maria, RS, Brazil.
Mol Cell Biochem. 2019 Feb;452(1-2):105-110. doi: 10.1007/s11010-018-3416-7. Epub 2018 Jul 31.
Thymol is a phytochemical component present in many plants used as food additive in order to promote animal growth due to its several biological properties. However, possible side effects of thymol remain poorly known limited to few reports. In this sense, we evaluated the enzymes of the purinergic signaling such as, ectonucleoside triphosphate diphosphohydrolase (NTPDase), 5'-nucleotidase and adenosine deaminase (ADA), that play an important role on toxicity induced by excessive adenosine triphosphate (ATP) content in the extracellular environment. Thus, the aim of this study was to evaluate whether purinergic signaling could be considered a potential target of thymol-induced inflammation, and the toxicity in tissues and immune cells of mice after thymol administration. NTPDase activity (ATP as substrate) in serum, spleen, and splenic lymphocytes was lower after 30 days of oral treatment at doses of 10, 20, and 40 mg/kg of thymol, while ADA activity was stimulated at 20 and 40 mg/kg. No differences were observed between groups regarding NTPDase (ADP as substrate) and 5'-nucleotidase activities in all evaluated tissues. Based on these evidences, adenine nucleotide hydrolysis is modified in serum, spleen, and splenic lymphocytes of mice treated with thymol, contributing to inflammation and toxicity by a reduction on ATP hydrolyses and its possible accumulation in the extracellular medium and increased Ado desamination and its possible reduction in the extracellular environment, leading to a self-sustained pro-inflammatory deleterious cycle. In summary, all tested thymol concentrations induced inflammation and toxicity in tissues and immune cells of treated mice.
百里香酚是许多用作食品添加剂的植物中的一种植物化学物质成分,由于其多种生物学特性,可促进动物生长。然而,百里香酚的可能副作用知之甚少,仅限于少数报道。从这个意义上说,我们评估了嘌呤能信号传导的酶,例如三磷酸核苷二磷酸水解酶(NTPDase)、5'-核苷酸酶和腺苷脱氨酶(ADA),它们在外周环境中过多三磷酸腺苷(ATP)含量诱导的毒性中发挥重要作用。因此,本研究旨在评估嘌呤能信号是否可以被认为是百里香酚诱导的炎症和毒性的潜在靶点,以及百里香酚给药后小鼠组织和免疫细胞的毒性。在口服治疗 30 天后,血清、脾脏和脾淋巴细胞中的 NTPDase 活性(以 ATP 为底物)在 10、20 和 40 mg/kg 百里香酚的剂量下降低,而 ADA 活性在 20 和 40 mg/kg 时受到刺激。在所有评估的组织中,各组之间的 NTPDase(以 ADP 为底物)和 5'-核苷酸酶活性均无差异。基于这些证据,用百里香酚处理的小鼠的血清、脾脏和脾淋巴细胞中的腺嘌呤核苷酸水解被改变,通过减少 ATP 水解及其在外周介质中的可能积累以及增加腺苷脱氨酶及其在外周环境中的可能减少,导致自我维持的促炎有害循环,从而导致炎症和毒性。总之,所有测试的百里香酚浓度都会在治疗小鼠的组织和免疫细胞中引起炎症和毒性。