ABSTRACT
Early warning signs of the outbreak of pandemic disease become a high profile from the beginning and they remind more susceptible individuals to keep social distance on social occasions. However, these signs have no way to the Susceptible–Infected–Recovered (SIR) models which have been concerned by medical scientists. Warning signs imply the risk level of the pandemic disease evaluated by the government. The response of susceptible population (S-population) to the warning signs is represented by a chicken game. In order to get a better payoff, the more beneficial behavior of the S-population may be induced in the autonomous society based on the SIR model. We emphasize that participants can choose their strategies whether to follow the health rules or not without coercion in the chicken game while the warning signs released by the policy makers can encourage S-population to choose beneficial behavior, instead of purely following the healthy rules or not. The agile policy helps S-population to make a choice on the basis of risk interests but without losing to protect themselves in a serious pandemic situation. Comparing the classic SIR model with our signal-SIR model, the serious pandemic signal released by the policy makers and the disease awareness to it together play an important role in the outbreak period of the pandemic disease. [ FROM AUTHOR]
ABSTRACT
17,18-Epoxyeicosatetraenoic acid (17,18-EEQ) and 19,20-epoxydocosapentaenoic acid (19,20-EDP) are bioactive epoxides produced from n-3 polyunsaturated fatty acid eicosapentaenoic acid and docosahexaenoic acid, respectively. However, these epoxides are quickly metabolized into less active diols by soluble epoxide hydrolase (sEH). We have previously demonstrated that an sEH inhibitor, t-TUCB, decreased serum triglycerides (TG) and increased lipid metabolic protein expression in the brown adipose tissue (BAT) of diet-induced obese mice. This study investigates the preventive effects of t-TUCB (T) alone or combined with 19,20-EDP (T + EDP) or 17,18-EEQ (T + EEQ) on BAT activation in the development of diet-induced obesity and metabolic disorders via osmotic minipump delivery in mice. Both T + EDP and T + EEQ groups showed significant improvement in fasting glucose, serum triglycerides, and higher core body temperature, whereas heat production was only significantly increased in the T + EEQ group. Moreover, both the T + EDP and T + EEQ groups showed less lipid accumulation in the BAT. Although UCP1 expression was not changed, PGC1α expression was increased in all three treated groups. In contrast, the expression of CPT1A and CPT1B, which are responsible for the rate-limiting step for fatty acid oxidation, was only increased in the T + EDP and T + EEQ groups. Interestingly, as a fatty acid transporter, CD36 expression was only increased in the T + EEQ group. Furthermore, both the T + EDP and T + EEQ groups showed decreased inflammatory NFκB signaling in the BAT. Our results suggest that 17,18-EEQ or 19,20-EDP combined with t-TUCB may prevent high-fat diet-induced metabolic disorders, in part through increased thermogenesis, upregulating lipid metabolic protein expression, and decreasing inflammation in the BAT.