A new study by Chinese researchers suggests that alternate day fasting (ADF), a popular diet trend, may worsen atherosclerosis, a condition where plaque builds up in the arteries and can lead to heart disease. The findings, published in the journal Life Metabolism in March 2024, raise concerns about the potential harmful effects of ADF in people at high risk for atherosclerosis.
The study, conducted by scientists from Nanfang Hospital of Southern Medical University and Shanxi Medical University Second Hospital, used mice that are prone to developing atherosclerosis. They found that ADF aggravated the formation of atherosclerotic lesions in these mice when they were fed a Western diet high in fat and cholesterol.
Although ADF helped prevent obesity, high blood sugar, and fatty liver in the mice, it also increased cholesterol levels in the liver and bloodstream. The researchers discovered that this effect was caused by ADF reducing the expression of a protein called ATF3 in the liver.
“This study provided novel insights into the effects of ADF on atherosclerosis by verifying that the deteriorated cholesterol profiles under ADF intervention might contribute to the worsened atherosclerosis in Apoe-/- mice fed with WD,” the authors stated in the press release.
The study also found that increasing ATF3 levels in the liver could reduce the negative effects of ADF on atherosclerosis. The expression of ATF3 was found to be regulated by another protein called KLF6, and both proteins were influenced by a cellular stress response pathway in the liver.
“Meanwhile, the study indicated that ADF inhibited hepatic ISR signaling pathway and KLF6 expression, and unraveled the previously unknown regulative effects of transcription factor KLF6 on hepatic ATF3 expression,” the authors added.
The findings suggest that ADF may have harmful effects in individuals at high risk for atherosclerosis and highlight the important role of the ATF3 protein in the liver in mediating the effects of ADF on cholesterol metabolism and atherosclerosis.
While more research is needed to fully understand the impact of ADF on human health, this study provides new insights into the complex relationship between diet, liver function, and cardiovascular disease risk.
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Chinese scientists provide novel insights into the effects of alternate day fasting on atherosclerosis
Atherosclerosis is the major contributor to cardiovascular mortality worldwide. Diet-induced metabolic abnormalities including obesity, hyperglycemia, dyslipidemia, insulin resistance (IR), and non-alcoholic fatty liver disease are considered atherogenic risk factors. Alternate day fasting (ADF) has gained growing attention due to its dramatic effects on improving disordered metabolic parameters. However, the roles of ADF in obesity-related cardiovascular diseases remain to be addressed, as the effects of ADF on atherosclerotic plaque formation remain inconsistent and controversial in atherosclerotic animal models.
Using atherogenic mice lacking apolipoprotein E (Apoe−/−), scientists from Nanfang Hospital of Southern Medical University and Shanxi Medical University Second Hospital have worked jointly and reported that ADF aggravated Western diet (WD)-induced atherosclerotic lesion formation, and they also validated that such effects were mediated by inhibiting the expression of hepatic activating transcription factor 3 (ATF3) under ADF intervention. The findings suggest the potentially harmful effects when ADF intervention is applied to the population at high risk of atherosclerosis. This study entitled “Alternate day fasting aggravates atherosclerosis through the suppression of hepatic ATF3 in Apoe−/− mice” was published online in Life Metabolism in March, 2024.
In this study, 11-week-old male Apoe−/− mice fed with WD were randomly grouped to ad libitum and ADF group. ADF aggravated WD-induced early and advanced atherosclerotic lesion formation in Apoe-/- mice. Although ADF protected Apoe−/− mice from obesity, hyperglycemia, and fatty liver and promoted energy expenditure, it deteriorated cholesterol profiles as hepatic cholesterol content and circulating cholesterol levels were increased. Liver RNA sequencing results in these mice demonstrated that ADF treatment significantly inhibited the hepatic integrated stress response (ISR) and decreased hepatic ATF3 expression. Hepatocyte-specific overexpression of Atf3 attenuated the effects of ADF on atherosclerotic plaque formation (Figure 1), indicating that the suppressed ATF3 expression in the liver was one of the contributing factors that mediated the modulatory effects of ADF on hepatic cholesterol accumulation and circulating cholesterol profile. The expression of ATF3 had a significant relevance with the expression of Krüppel-like factor 6 (KLF6), which is a zinc finger transcription factor. In hepatocytes treated with ISR stressor, the expression of ATF3 could be regulated by KLF6, and both the expressions of ATF3 and KLF6 were regulated by the hepatic cellular ISR pathway. Mechanistically, ADF inhibited hepatic ISR and decreased the expression of KLF6 and ATF3.
This study provided novel insights into the effects of ADF on atherosclerosis by verifying that the deteriorated cholesterol profiles under ADF intervention might contribute to the worsened atherosclerosis in Apoe-/- mice fed with WD. Meanwhile, the study indicated that ADF inhibited hepatic ISR signaling pathway and KLF6 expression, and unraveled the previously unknown regulative effects of transcription factor KLF6 on hepatic ATF3 expression. ATF3 could act as a downstream component of ISR in the liver and the study shed light on the role of hepatic ATF3 in mediating the effects of ADF on atherosclerosis, thus providing evidence supporting the diverse effects of hepatic ISR in regulating cholesterol metabolism and atherosclerosis.
