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腺苷通过小鼠肾上腺-肝脏串扰刺激肝糖原分解。

Adenosine stimulates hepatic glycogenolysis via adrenal glands-liver crosstalk in mice.

机构信息

Department of Nutritional Science, Faculty of Applied Bioscience, Tokyo University of Agriculture, Tokyo, Japan.

出版信息

PLoS One. 2018 Dec 21;13(12):e0209647. doi: 10.1371/journal.pone.0209647. eCollection 2018.

DOI:10.1371/journal.pone.0209647
PMID:30576384
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6303095/
Abstract

Adenosine signaling is involved in glucose metabolism in hepatocytes and myocytes in vitro. However, no information is available regarding the effect of adenosine on glucose metabolism in vivo. Thus, we examined how extracellular adenosine acts on glucose metabolism using mice. Subcutaneous injections of adenosine (10, 25, and 50 mg/kg bodyweight) dose-dependently increased blood glucose levels, with the peak occurring at 30 min post injection. At 30 min after adenosine injection (25 mg/kg bodyweight), glycogen content in the liver, but not the skeletal muscle, was significantly decreased. Hepatic glycogen depletion by fasting for 12 h suppressed the increase of blood glucose levels at 30 min after adenosine injection. These results suggest that adenosine increases blood glucose levels by stimulating hepatic glycogenolysis. To investigate the effect of adenosine on the adrenal gland, we studied the glycogenolysis signal in adrenalectomized (ADX) mice. Adenosine significantly increased the blood glucose levels in sham mice but not in the ADX mice. The decrease in hepatic glycogen content induced by adenosine in the sham mice was partially suppressed in the ADX mice. The level of plasma corticosterone, the main glucocorticoid in mice, was significantly increased in the sham mice by adenosine but its levels were low in ADX mice injected with either PBS or adenosine. These results suggest that adenosine promotes secretion of corticosterone from the adrenal glands, which causes hepatic glycogenolysis and subsequently the elevation of blood glucose levels. Our findings are useful for clarifying the physiological functions of adenosine in glucose metabolism in vivo.

摘要

腺嘌呤核苷信号参与了肝细胞和心肌细胞的体外葡萄糖代谢。然而,目前尚无关于腺嘌呤核苷对体内葡萄糖代谢影响的信息。因此,我们使用小鼠研究了细胞外腺嘌呤核苷如何作用于葡萄糖代谢。腺嘌呤核苷(10、25 和 50mg/kg 体重)的皮下注射剂量依赖性地增加了血糖水平,峰值出现在注射后 30 分钟。在注射腺嘌呤核苷 30 分钟后(25mg/kg 体重),肝脏而不是骨骼肌中的糖原含量显著减少。禁食 12 小时导致肝糖原耗竭,抑制了注射腺嘌呤核苷 30 分钟后血糖水平的升高。这些结果表明,腺嘌呤核苷通过刺激肝糖原分解来增加血糖水平。为了研究腺嘌呤核苷对肾上腺的影响,我们研究了肾上腺切除术(ADX)小鼠中的糖原分解信号。腺嘌呤核苷显著增加了假手术小鼠的血糖水平,但对 ADX 小鼠没有影响。腺嘌呤核苷在假手术小鼠中引起的肝糖原含量减少在 ADX 小鼠中部分受到抑制。腺嘌呤核苷显著增加了假手术小鼠的血浆皮质酮水平,皮质酮是小鼠中的主要糖皮质激素,但 ADX 小鼠注射 PBS 或腺嘌呤核苷后皮质酮水平较低。这些结果表明,腺嘌呤核苷促进了肾上腺皮质酮的分泌,从而导致肝糖原分解,随后血糖水平升高。我们的发现有助于阐明体内腺嘌呤核苷在葡萄糖代谢中的生理功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec6c/6303095/9dac5e00caa9/pone.0209647.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec6c/6303095/1d3041579f61/pone.0209647.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec6c/6303095/58e06a4a2fa3/pone.0209647.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec6c/6303095/9e03ea7b7cd0/pone.0209647.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec6c/6303095/d6a07d725985/pone.0209647.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec6c/6303095/9dac5e00caa9/pone.0209647.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec6c/6303095/1d3041579f61/pone.0209647.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec6c/6303095/58e06a4a2fa3/pone.0209647.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec6c/6303095/9e03ea7b7cd0/pone.0209647.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec6c/6303095/d6a07d725985/pone.0209647.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec6c/6303095/9dac5e00caa9/pone.0209647.g005.jpg

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