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黄芩素,一种黄酮类化合物,对脂肪细胞代谢的调节作用。

Regulatory effects of baicalin, a flavonoid compound, on adipocyte metabolism.

机构信息

Department of Animal Physiology, Biochemistry and Biostructure, Poznan University of Life Sciences, Poznan, Poland.

出版信息

J Physiol Pharmacol. 2023 Aug;74(4). doi: 10.26402/jpp.2023.4.05. Epub 2023 Oct 16.

DOI:10.26402/jpp.2023.4.05
PMID:37865958
Abstract

Baicalin is a plant-derived, biologically active compound exerting numerous advantageous effects. Adipocytes store and release energy in the process of lipogenesis and lipolysis. Rodent studies have shown that baicalin treatment positively affects fat tissue, however, data on the direct influence of this compound on adipocyte metabolism is lacking. In the present research, the short-term effects of 25, 50, and 100 μM baicalin on glucose transport, conversion to lipids, and oxidation, and also on lipolysis in primary rat adipocytes were explored. Lipolysis was measured as glycerol release from adipocytes. It was shown that 100 μM baicalin reduced glucose oxidation but at any concentration did not affect glucose transport and lipogenesis. Baicalin significantly increased the adipocyte response to physiological and pharmacological lipolytic stimuli (such as epinephrine - adrenergic agonist, DPCPX - adenosine A receptor antagonist, and amrinone - cAMP phosphodiesterase inhibitor). The stimulatory effects of baicalin on epinephrine-induced lipolysis were markedly diminished by insulin (activator of cAMP phosphodiesterases) and H-89 (PKA inhibitor). It was also demonstrated that baicalin evoked a similar rise in epinephrine-induced lipolysis in the presence of glucose and alanine. Our results provided evidence that baicalin may reduce glucose oxidation and is capable of enhancing lipolysis in primary rat adipocytes. The action on lipolysis is glucose-independent and covers both the adrenergic and adenosine A receptor pathways. The rise in cAMP content is proposed to be responsible for the observed potentiation of the lipolytic process.

摘要

黄芩苷是一种植物来源的生物活性化合物,具有多种有益作用。脂肪细胞在脂肪生成和脂肪分解过程中储存和释放能量。啮齿动物研究表明,黄芩苷治疗对脂肪组织有积极影响,然而,缺乏关于该化合物对脂肪细胞代谢直接影响的数据。在本研究中,探索了 25、50 和 100μM 黄芩苷对原代大鼠脂肪细胞葡萄糖转运、转化为脂质和氧化以及脂肪分解的短期影响。脂肪分解通过从脂肪细胞释放甘油来测量。结果表明,100μM 黄芩苷降低了葡萄糖氧化,但在任何浓度下都不影响葡萄糖转运和脂肪生成。黄芩苷显著增加了脂肪细胞对生理和药理学脂肪分解刺激(如肾上腺素-肾上腺素能激动剂、DPCPX-腺苷 A 受体拮抗剂和氨力农-cAMP 磷酸二酯酶抑制剂)的反应。胰岛素(cAMP 磷酸二酯酶激活剂)和 H-89(PKA 抑制剂)显著减弱了黄芩苷对肾上腺素诱导的脂肪分解的刺激作用。还证明,在葡萄糖和丙氨酸存在的情况下,黄芩苷引起肾上腺素诱导的脂肪分解相似增加。我们的结果提供了证据,表明黄芩苷可能降低葡萄糖氧化,并能够增强原代大鼠脂肪细胞的脂肪分解。这种作用与葡萄糖无关,涵盖了肾上腺素能和腺苷 A 受体途径。cAMP 含量的增加被认为是观察到的脂肪分解过程增强的原因。

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