400038 重庆,陆军军医大学(第三军医大学)第一附属医院心血管内科,重庆市介入心脏病学研究所
Received:15 December 2017,
Revised:2018-03-15,
Published:30 May 2018
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Chenliang ZHANG, Yizhang LIN, Xin ZHOU, et al. Effect of high salt intake on browning of white adipose tissue in mice and mechanism of its central regulation[J]. Journal of Third Military Medical University, 2018, 40(10): 868-874.
Chenliang ZHANG, Yizhang LIN, Xin ZHOU, et al. Effect of high salt intake on browning of white adipose tissue in mice and mechanism of its central regulation[J]. Journal of Third Military Medical University, 2018, 40(10): 868-874. DOI: 10.16016/j.1000-5404.201712261.
目的
2
研究高盐摄入对小鼠白色脂肪组织(white adipose tissue,WAT)棕色化的影响,探讨其可能的中枢调控机制。
方法
2
采用随机数字表法将20只8周龄的C57BL/6J小鼠分为4组(
n
=5):短期高盐组与短期对照组(饲养24 h后处死,免疫组化法检测小鼠大脑c-Fos表达情况),长期高盐组与长期对照组(连续饲养8周,每周对体质量、体温、饮水、进食进行监测)。对照组正常饮水,高盐组给予含2%氯化钠的盐水。长期组实验结束后收集血清检测血脂水平。收集性腺脂肪和脑标本,用荧光定量PCR法检测性腺脂肪组织中解耦联蛋白-1(uncoupling protein-1,UCP-1)等棕色化相关调控基因的改变以及下丘脑室旁核脑源性生长因子(brain derived neurotrophic factor,BDNF)的mRNA表达。
结果
2
短期高盐刺激后,小鼠下丘脑室旁核c-Fos表达高盐组(112.67±11.24)较对照组(30.67±5.51)明显增加(
P
<
0.01)。给予小鼠8周的高盐刺激后,小鼠血中甘油三酯[(0.75±0.19)mmol/L
vs
(1.07±0.08)mmol/L,
P
<
0.05
]
和游离脂肪酸含量下降[(0.64±0.14)mmol/L
vs
(0.92±0.15)mmol/L,
P
<
0.05
]
,单侧
性腺脂肪质量明显减轻[(0.11±0.01)g
vs
(0.15±0.01)g,
P
<
0.01
]
。荧光定量PCR法检测发现高盐组WAT棕色化标志基因UCP-1含量(4.62±0.94)较对照组(1.00±0.16)明显增加(
P
<
0.01);下丘脑室旁核BDNF高盐组mRNA表达(3.14±0.31)较对照组(1.00±0.12)明显增加(
P
<
0.01)。
结论
2
长期高盐可诱导小鼠WAT棕色化,而下丘脑室旁核BDNF参与了其中的中枢调控过程。
Objective
2
To investigate the effect of high salt intake on the browning of white adipose tissue (WAT) in mice and explore the central regulatory mechanism underlying this effect.
Methods
2
Twenty male C57BL/6J mice were randomly allocated into control and high salt intake groups and were given free access to normal water and 2% NaCl solution
respectively. Each group was further divided into 2 subgroups for observation at 24 h and at 8 weeks. The mice in 24 h groups were sacrificed for immunohistochemistry of c-Fos expression in the brain at 24 h. In 8 weeks groups
the mice were examined for body weight
body temperature
water intake and food intake on a weekly basis for 8 weeks
after which the mice were sacrificed for measurement of blood lipid levels and detection of mRNA expression of uncoupling protein-1 (UCP-1) in epididymal WAT and brain derived neurotrophic factor (BDNF) in the paraventricular nucleus (PVN) using qRT-PCR.
Results
2
The mice with high salt intake for 24 h showed significantly increased number of c-Fos-positive neurons in the PVN compared with the corresponding control group (112.67±11.24
vs
30.67±5.51
P
<
0.01). Compared with the control group
high-salt intake for 8 weeks caused a significant decrease in the weight of WAT (0.11±0.01
vs
0.15±0.01 g
P
<
0.01)
content of TG (0.75±0.19
vs
1.07±0.08 mmol/L
P
<
0.05) and levels of free fatty acids (0.64±0.14
vs
0.92±
0.15 mmol/L
P
<
0.05)
and significantly increased the transcriptional level of UCP-1 in the WAT (4.62±0.94
vs
1.00±0.16
P
<
0.01) and the mRNA expression of BDNF in the PVN (3.14±0.31
vs
1.00±0.12
P
<
0.01).
Conclusion
2
Long-term high salt intake can induce the browning of WAT
and BDNF in the PVN participates in the central regulation of this process.
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