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[松花粉干预卵巢早衰大鼠肝脏的伪靶向代谢组学分析]

[Pseudotargeted metabolomics analysis of pine pollen intervention in the liver of premature ovarian failure rats].

作者信息

Qu Tao, Chen Yang, Yang Changjun, Liu Qisong, Chen Hui, He Zhiyong, Wang Zhaojun, Chen Jie, Zeng Maomao

机构信息

2. New Era Health Industry (Group) Co., Ltd., Yantai 264006, China.

1. State Key Laboratory of Food Science and Technology, Jiangnan University, Wuxi 214122, China.

出版信息

Se Pu. 2023 Jan;41(1):47-57. doi: 10.3724/SP.J.1123.2022.04017.

Abstract

Premature ovarian failure (POF) is a prevalent gynecological disease. In traditional Chinese medicine, it is believed that POF is directly related to abnormal function of the liver and kidneys. As such, regulation of the liver metabolism through the use of medicinal and edible substances is important for the treatment of POF. Pine pollen, a traditional Chinese medicinal and edible pollen variety, contains various active substances, such as sex hormones and phytohormones, which have been used to inhibit inflammation, regulate the immune system, and protect reproductive tissues. Using ultra-high performance liquid chromatography-triple quadrupole mass spectrometry (UHPLC-MS/MS), this study examined the influence of pine pollen on the liver metabolome of cyclophosphamide-induced POF model Sprague Dawley (SD) rats. The variations in the metabolites present in the liver tissue of control SD rats, model SD rats, and SD rats treated with various doses of pine pollen or estrogen were analyzed using principal component analysis (PCA) in combination with orthogonal partial least squares discriminant analysis (OPLS-DA) and other multivariate statistical methods to reveal the mechanism of pine pollen intervention in the livers of POF SD rats. An animal model experiment was conducted using six groups of ten-week-old rats. Cyclophosphamide was administered intraperitoneally to the model group and four intervention groups at a dosage of 60 mg/kg for 1 d followed by a dosage of 10 mg/kg for 14 d. Within the following four weeks, each of the four intervention groups received the intragastric administration of 0.1, 0.5, or 1.5 g/kg bodyweight (BW) of pine pollen, or 0.075 g/kg BW of conjugated estrogens (positive control). Equal quantities of normal saline were administered to the control and cyclophosphamide-treated model groups. Subsequently, the rat livers were subject to pseudotargeted metabolomics, and a total of 687 liver metabolites were discovered using both positive and negative ions. The metabolites differing in content were screened using the -test (<0.05) and the fold change (FC>2 or <0.5) in univariate analysis, and the variable importance in projection (VIP>1) in multivariate analysis. It was found that in comparison with the control group, the contents of 32 metabolites significantly increased, while those of 28 metabolites significantly decreased in the model group. The majority of these metabolites were involved -linolenic acid metabolism, vitamin B6 metabolism, and purine metabolism, along with the lysine degradation and glycolysis/gluconeogenesis metabolic pathways. Compared with the cyclophosphamide-induced model group, the estrogen group exhibited increased levels of 47 metabolites and decreased levels of 29 metabolites, wherein 34 metabolites were restored to the levels found in the control group. These metabolites mainly involved the vitamin B6, lysine, glycolysis/gluconeogenesis, arginine and proline, and cysteine and methionine metabolic pathways. In the low/medium/high-dose pine pollen groups, the contents of 34/32/34 metabolites increased, the contents of 30/37/24 metabolites decreased, and the contents of 47/38/34 metabolites were restored to the levels found in the control group, respectively. These metabolites were mainly involved in vitamin B6 metabolism, purine metabolism, and the glycolysis/gluconeogenesis metabolic pathway. These results therefore indicate that the restoring effect of pine pollen is equivalent or superior to that of conjugated estrogen. Additionally, based on the known metabolic pathways, it appears that when estrogen interferes with the liver metabolism, the key metabolic pathways that become affected are the arginine and proline metabolism and cysteine and methionine metabolism pathways. In contrast, pine pollen intervention affected existing metabolic pathways that were known to be disordered by cyclophosphamide. The use of pine pollen may therefore restore the levels of many metabolites. It should be noted that 23 overlaps exist between the estrogen-restored metabolites and the pine pollen-restored metabolites, including a variety of acylcarnitines, such as ACar 10∶0. As a result, pine pollen extract may be able to normalize the liver metabolic abnormalities induced by POF. This study therefore establishes a theoretical reference for the development of functional applications for pine pollen and for the treatment of POF.

摘要

卵巢早衰(POF)是一种常见的妇科疾病。在中医中,认为POF与肝肾的功能异常直接相关。因此,通过使用药食两用物质调节肝脏代谢对POF的治疗很重要。松花粉是一种传统的药食两用花粉品种,含有多种活性物质,如性激素和植物激素,已被用于抑制炎症、调节免疫系统和保护生殖组织。本研究采用超高效液相色谱-三重四极杆质谱(UHPLC-MS/MS),研究了松花粉对环磷酰胺诱导的POF模型Sprague Dawley(SD)大鼠肝脏代谢组的影响。采用主成分分析(PCA)结合正交偏最小二乘判别分析(OPLS-DA)等多元统计方法,分析对照SD大鼠、模型SD大鼠以及用不同剂量松花粉或雌激素处理的SD大鼠肝脏组织中代谢物的变化,以揭示松花粉对POF SD大鼠肝脏的干预机制。使用六组十周龄大鼠进行动物模型实验。模型组和四个干预组腹腔注射环磷酰胺,剂量为60 mg/kg,持续1天,随后剂量为10 mg/kg,持续14天。在接下来的四周内,四个干预组分别灌胃给予0.1、0.5或1.5 g/kg体重(BW)的松花粉,或0.075 g/kg BW的结合雌激素(阳性对照)。对照和环磷酰胺处理的模型组给予等量的生理盐水。随后,对大鼠肝脏进行准靶向代谢组学分析,使用正离子和负离子共发现687种肝脏代谢物。在单变量分析中,使用t检验(<0.05)和倍数变化(FC>2或<0.5)筛选含量不同的代谢物,在多变量分析中使用变量重要性投影(VIP>1)。结果发现,与对照组相比,模型组中32种代谢物的含量显著增加,28种代谢物的含量显著降低。这些代谢物大多参与了γ-亚麻酸代谢、维生素B6代谢和嘌呤代谢,以及赖氨酸降解和糖酵解/糖异生代谢途径。与环磷酰胺诱导的模型组相比,雌激素组有47种代谢物水平升高,29种代谢物水平降低,其中34种代谢物恢复到对照组水平。这些代谢物主要涉及维生素B6、赖氨酸、糖酵解/糖异生、精氨酸和脯氨酸以及半胱氨酸和蛋氨酸代谢途径。在低/中/高剂量松花粉组中,分别有34/32/34种代谢物含量增加,30/37/24种代谢物含量降低,47/38/34种代谢物含量恢复到对照组水平。这些代谢物主要参与维生素B6代谢、嘌呤代谢和糖酵解/糖异生代谢途径。因此,这些结果表明松花粉的恢复作用等同于或优于结合雌激素。此外,基于已知的代谢途径,当雌激素干扰肝脏代谢时,受影响的关键代谢途径似乎是精氨酸和脯氨酸代谢以及半胱氨酸和蛋氨酸代谢途径。相比之下,松花粉干预影响了已知因环磷酰胺而紊乱的现有代谢途径。因此,使用松花粉可能会恢复许多代谢物的水平。需要注意的是,雌激素恢复的代谢物与松花粉恢复的代谢物之间存在23个重叠,包括多种酰基肉碱,如ACar 10∶0。因此,松花粉提取物可能能够使POF诱导的肝脏代谢异常正常化。本研究因此为松花粉的功能应用开发和POF的治疗建立了理论参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eae1/9837668/93e147c3bab6/cjc-41-01-47-img_1.jpg

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