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Remote Effects of Transplanted Perivascular Adipose Tissue on Endothelial Function and Atherosclerosis
被引:43
|作者:
Horimatsu, Tetsuo
[1
]
Patel, Aaron S.
[1
]
Prasad, Rosaria
[1
]
Reid, Lauren E.
[1
]
Benson, Tyler W.
[1
]
Zarzour, Abdalrahman
[1
]
Ogbi, Mourad
[1
]
do Nascimento, Thiago Bruder
[1
]
de Chantemele, Eric Belin
[1
]
Stansfield, Brian K.
[2
]
Lu, Xin-Yun
[3
]
Kim, Ha Won
[1
]
Weintraub, Neal L.
[1
]
机构:
[1] Augusta Univ, Med Coll Georgia, Vasc Biol Ctr, Dept Med,Cardiol Div, 1460 Laney Walker Blvd, Augusta, GA 30912 USA
[2] Augusta Univ, Med Coll Georgia, Pediat & Vasc Biol Ctr, Augusta, GA USA
[3] Augusta Univ, Med Coll Georgia, Dept Neurosci & Regenerat Med, Augusta, GA USA
基金:
美国国家卫生研究院;
关键词:
Perivascular adipose tissue;
Fat transplantation;
Endothelial dysfunction;
Atherosclerosis;
Inflammation;
NITRIC-OXIDE SYNTHASE;
NEOINTIMAL HYPERPLASIA;
ADIPONECTIN;
INFLAMMATION;
DELETION;
D O I:
10.1007/s10557-018-6821-y
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
PurposePerivascular adipose tissue (PVAT) surrounds the arterial adventitia and plays an important role in vascular homeostasis. PVAT expands in obesity, and inflamed PVAT can locally promote endothelial dysfunction and atherosclerosis. Here, using adipose tissue transplantation, we tested the hypothesis that expansion of PVAT can also remotely exacerbate vascular disease.MethodsFifty milligrams of abdominal aortic PVAT was isolated from high-fat diet (HFD)-fed wild-type mice and transplanted onto the abdominal aorta of lean LDL receptor knockout mice. Subcutaneous and visceral adipose tissues were used as controls. After HFD feeding for 10weeks, body weight, glucose/insulin sensitivity, and lipid levels were measured. Adipocytokine gene expression was assessed in the transplanted adipose tissues, and the thoracic aorta was harvested to quantify atherosclerotic lesions by Oil-Red O staining and to assess vasorelaxation by wire myography.ResultsPVAT transplantation did not influence body weight, fat composition, lipid levels, or glucose/insulin sensitivity. However, as compared with controls, transplantation of PVAT onto the abdominal aorta increased thoracic aortic atherosclerosis. Furthermore, PVAT transplantation onto the abdominal aorta inhibited endothelium-dependent relaxation in the thoracic aorta. MCP-1 and TNF- expression was elevated, while adiponectin expression was reduced, in the transplanted PVAT tissue, suggesting augmented inflammation as a potential mechanism for the remote vascular effects of transplanted PVAT.ConclusionsThese data suggest that PVAT expansion and inflammation in obesity can remotely induce endothelial dysfunction and augment atherosclerosis. Identifying the underlying mechanisms may lead to novel approaches for risk assessment and treatment of obesity-related vascular disease.
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页码:503 / 510
页数:8
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