Pitavastatin attenuates hypercholesterolemia-induced decline in serotonin transporter availability

被引:1
作者
Chen, Sy-Jou [1 ]
Cho, Rou-Ling [2 ]
Yeh, Skye Hsin-Hsien [3 ,4 ]
Tsai, Min-Chien [5 ]
Chuang, Yi-Ping [6 ,7 ]
Lien, Chih-Feng [2 ]
Chiu, Chuang-Hsin [8 ]
Yeh, Yi-Wei [9 ]
Lin, Chin-Sheng [2 ]
Ma, Kuo-Hsing [10 ]
机构
[1] Triserv Gen Hosp, Natl Def Med Ctr, Dept Emergency Med, Taipei 114, Taiwan
[2] Triserv Gen Hosp, Natl Def Med Ctr, Dept Internal Med, Div Cardiol, Taipei 114, Taiwan
[3] Natl Def Med Ctr, Sch Med, Taipei, Taiwan
[4] Natl Yang Ming Chaio Tung Univ, Brain Res Ctr, Taipei, Taiwan
[5] Grad Inst Physiol, Natl Def Med Ctr, Dept Physiol & Biophys, Taipei, Taiwan
[6] Natl Def Med Ctr, Dept Microbiol & Immunol, Taipei, Taiwan
[7] Natl Def Med Ctr, Grad Inst Microbiol & Immunol, Taipei, Taiwan
[8] Triserv Gen Hosp, Natl Def Med Ctr, Dept Nucl Med, Taipei, Taiwan
[9] Triserv Gen Hosp, Natl Def Med Ctr, Dept Psychiat, Taipei, Taiwan
[10] Natl Def Med Ctr, Dept Biol & Anat, Taipei 114, Taiwan
关键词
Pitavastatin; Hypercholesterolemia; 4-[F-18]-ADAM; Positron emission tomography; Serotonin transporter (SERT); Depression; MAJOR DEPRESSIVE DISORDER; INCREASED RISK; STATIN USE; CHOLESTEROL; HYPERLIPIDEMIA; INFLAMMATION; METAANALYSIS; ANXIETY; PATHOPHYSIOLOGY; SUBSTRATE;
D O I
10.1186/s12944-024-02236-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Introduction Hypercholesterolemia is associated with increased inflammation and impaired serotonin neurotransmission, potentially contributing to depressive symptoms. However, the role of statins, particularly pitavastatin, in modulating serotonin transporter (SERT) function within this context remains underexplored. This study aimed to investigate whether pitavastatin counteracts the neurobiological effects of hypercholesterolemia. Methods Low-density lipoprotein receptor knockout (LDLR-/-) mice on a C57BL/6 background were assigned to three groups: a control group fed a standard chow diet, a group fed a high-fat diet (HFD), and a third group fed a high-fat diet supplemented with pitavastatin (HFD + Pita). We evaluated the effects of HFD with or without pitavastatin on lipid profiles, inflammatory markers, and SERT availability using small-animal positron emission tomography (PET) scans with the radioligand 4-[F-18]-ADAM over a 20-week period. Results Pitavastatin treatment in HFD-fed mice significantly reduced both total cholesterol and LDL cholesterol levels in HFD-fed mice compared to those on HFD alone. Elevated inflammatory markers such as IL-1 alpha, MCP-1/CCL2, and TNF-alpha in HFD mice were notably decreased in the HFD + Pita group. PET scans showed reduced SERT availability in the brains of HFD mice; however, pitavastatin improved this in brain regions associated with mood regulation, suggesting enhanced serotonin neurotransmission. Additionally, the sucrose preference test showed a trend towards increased preference in the HFD + Pita group compared to the HFD group, indicating a potential reduction in depressive-like behavior. Conclusion Our findings demonstrate that pitavastatin not only lowers cholesterol and reduces inflammation but also enhances SERT availability, suggesting a potential role in alleviating depressive symptoms associated with hypercholesterolemia. These results highlight the multifaceted benefits of pitavastatin, extending beyond its lipid-lowering effects to potentially improving mood regulation and neurotransmitter function.
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页数:14
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