ABSTRACT
Orexin-A is a peptide hormone that plays a crucial role in feeding regulation and energy homeostasis. Diurnal intermittent fasting (DIF) has been found to increase orexin-A plasma levels during fasting hours, while Ramadan fasting which resembles DIF, has led to beneficial effects on endothelial function. Herein, we aimed to investigate the effects of orexin-A on the expression of molecules involved in the atherogenesis process: Monocyte chemoattractant protein-1 (MCP-1), matrix metalloproteinases 2 and 9 (MMP-2 and MMP-9) and tissue inhibitor of metalloproteinase-1 and 2 (TIMP-1 and TIMP-2), in human aortic endothelial cells (HAECs). HAECs were incubated with orexin-A at concentrations of 40 ng/mL, 200 ng/mL and 400 ng/mL for 6, 12 and 24 h. The mRNA levels of MCP-1, MMP-2, MMP-9, TIMP-1, and TIMP-2 and orexin-1 receptor were measured by real-time qPCR. We also evaluated the MMP-2, p38, phospho-p38, NF-κΒ/p65 as well as TIMP-1 protein levels by Western blot and ELISA, respectively. MMP-2 activity was measured by gelatin zymography. Short-term 6-h incubation of HAECs with orexin-A at a high concentration (400 ng/mL) decreased MCP-1, MMP-2 expression, MMP-2/TIMP-1 ratio (p < 0.05), and MMP-2 activity, while incubation for 24 h increased MCP-1, MMP-2 expression (p < 0.05), MMP-2/TIMP-1 and MMP-2/TIMP-2 ratio (p < 0.01 and p < 0.05, respectively) as well as MMP-2 activity. The dual effects of orexin-A are mediated, at least in part, via regulation of p38 and NF-κΒ pathway. Orexin-A may have an equivocal role in atherosclerosis process with its effects depending on the duration of exposure.
Subject(s)
Atherosclerosis/prevention & control , Endothelial Cells/drug effects , Orexins/pharmacology , Cell Line , Cell Proliferation/drug effects , Cell Survival/drug effects , Chemokine CCL2/genetics , Chemokine CCL2/metabolism , Drug Administration Schedule , Gene Expression Regulation/drug effects , Humans , Matrix Metalloproteinase 2/genetics , Matrix Metalloproteinase 2/metabolism , Orexins/administration & dosage , Tissue Inhibitor of Metalloproteinase-1/genetics , Tissue Inhibitor of Metalloproteinase-1/metabolismABSTRACT
BACKGROUND: A limited number of pesticides are available for the control of soil pests in potato. This, together with the monoculture nature of potato cultivation, does not favour chemical rotation, increasing the risk of reduced biological efficacy due to microbial adaptation. The dissipation of three major organophosphates (chlorpyrifos, ethoprophos and fosthiazate) was studied in comparison with fipronil, an insecticide recently introduced in potato cultivation, in 17 soils from potato monoculture areas in Greece to explore the extent of enhanced biodegradation development. RESULTS: The dissipation time of the four pesticides varied in the different soils, with DT50 values of 1.7-30.8 days, 2.7-56 days, 7.0-31.0 days and 24.5-116.5 days for fosthiazate, chlorpyrifos, ethoprophos and fipronil, respectively. A rapid dissipation of ethoprophos and fosthiazate in two soils with previous exposure to these nematicides provided first evidence for the development of enhanced biodegradation. Sterilisation of the given soils inhibited the dissipation of fosthiazate. Additionally, fosthiazate dissipation in the soils increased upon repeated applications. CONCLUSION: The development of enhanced biodegradation of fosthiazate in soils from potato monoculture regions was verified. This is the first report of enhanced biodegradation for this chemical. Further studies will focus on the isolation of microorganisms responsible for the dissipation of fosthiazate.
