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Article

Coreopsis tinctoria and Its Flavonoids Ameliorate Hyperglycemia in Obese Mice Induced by High-Fat Diet

by
Feng Zhang
1,†,
Minglan Yang
1,2,†,
Jia Xu
1,
Yanzhou Hu
1,
Ruxin Gao
1,
Kunlun Huang
1,3 and
Xiaoyun He
1,3,*
1
Key Laboratory of Precision Nutrition and Food Quality, Ministry of Education, College of Food Science and Nutritional Engineering, China Agricultural University, Beijing 100083, China
2
Department of Clinical Nutrition, West China Hospital, Sichuan University, Chengdu 610041, China
3
Key Laboratory of Safety Assessment of Genetically Modified Organism (Food Safety), The Ministry of Agriculture and Rural Affairs of the P.R. China, Beijing 100083, China
*
Author to whom correspondence should be addressed.
†
These authors contributed to this work equally.
Nutrients 2022, 14(6), 1160; https://doi.org/10.3390/nu14061160
Submission received: 23 December 2021 / Revised: 17 February 2022 / Accepted: 18 February 2022 / Published: 9 March 2022
(This article belongs to the Special Issue Medicine and Food Homologous Plants and Human Health)
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Abstract

:
With the prevalence of obesity all over the world, human health has been seriously affected. In particular, the number of diabetic and cardiovascular diseases has increased dramatically. The herb Coreopsis tinctoria (C. tinctoria) shows diverse biological and pharmacological activities, which are mainly attributed to its flavonoids. However, the specific functional substances that play an active role in C. tinctoria remain unclear, and its mechanism has not been deeply explored. In this study, we established a diet-induced obesity (DIO) mice model and treated mice with C. tinctoria or kaempferol for 8 weeks. The results showed that both C. tinctoria and kaempferol lowered body weight, reduced fasting blood glucose, and improved glucose tolerance and insulin resistance to alleviate obesity in DIO mice. The level of hemoglobin A1c also decreased significantly after treatment with C. tinctoria and kaempferol. Moreover, the administration of C. tinctoria and kaempferol also restored gut microbiota imbalance and significantly increased Desulfovibrio and Butyricimonas levels, which have been reported to improve glucose metabolism and intestinal health. In general, our study shows that C. tinctoria is a potential hypoglycemic substance for obesity and may reduce blood glucose by regulating gut microbiota, and that kaempferol is one of the effective substances of C. tinctoria.

1. Introduction

In recent years, rates of global obesity have increased dramatically. According to World Health Organization (WHO) estimations, one in five adults will be obese by 2025 [1]. In fact, obesity has been almost considered as an epidemic worldwide, associated with diabetes mellitus, cardiovascular disease, fatty liver disease, osteoarthritis, obstructive sleep apnea, several cancers, as well as social and psychological problems [2,3]. Overweight and lack of physical activity are the main determinants of insulin resistance with hyperglycemia and hyperinsulinemia. Furthermore, reports indicate that severe obesity in childhood and adolescence increases the risk of type 2 diabetes (T2DM) in youth and young adults [4,5]. There is sufficient evidence that obesity management can delay the development of T2DM from pre-diabetes and may be beneficial to its treatment [6]. At present, most obesity or diabetes treatment methods have the disadvantages of significant side effects, easy rebound, decreased immunity, and so on [7,8]. Therefore, looking for a safe and effective way to lose weight and reduce blood glucose has become the consistent direction of public health efforts. In recent years, dietary intervention has become a main research hotspot [9].
Coreopsis tinctoria (C. tinctoria) is an annual herb that mainly grows in high-altitude areas above 3000 m in Xinjiang, China, especially the Hotan area [10]. Current studies have shown that its water extracts possess diverse biological and pharmacological activities, among them anti-diabetes, anti-cardiovascular diseases, antioxidant, and protective effects on organs [11,12,13,14]. C. tinctoria flower tea ameliorated hepatic steatosis, glucose intolerance, and insulin resistance in HFD rats, and the regulatory effects may be mediated via the Akt/FoxO1 signaling pathway [15]. A study showed that C. tinctoria tea administration could significantly increase the intestinal microbial richness and diversity of mice induced by a high-fat diet and improve gut microbiota composition to an approximately normal status, thereby regulating blood lipid metabolism [14]. The major bioactive components in C. tinctoria are the flavonoids [16,17]. Previous studies have found that the flavonoids from C. tinctoria extracts can reduce blood lipid by down-regulating adipose differentiation-related protein ADRP [18]. Kaempferol is a major flavonoid glycoside found in many natural products, also found in C. tinctoria, which displays several pharmacological properties, including anti-inflammatory, antioxidant, antitumor, neuroprotective, and antidiabetic activities [19,20]. It is not clear whether kaempferol is one of the hypoglycemic constituents of C. tinctoria.
In this study, we explored the hypoglycemic effects of water extract of C. tinctoria and kaempferol on a hyperglycemia model induced by a high-fat diet, and investigated whether the modulation of gut microbiota is the mechanism for C. tinctoria extracts and kaempferol to exert their effects on the hyperglycemia model.

2. Materials and Methods

2.1. Preparation of Water Extract of C. tinctoria and Single Flavonoids Substance

C. tinctoria was collected from the planting base 5500 m above sea level in Saitula, Xinjiang, China. The petals of the plants were crushed and sieved with a 60 mesh sieve with 0.3 mm square holes. Afterwards, C. tinctoria was collected using water as an extractant. C. tinctoria was extracted by rotating and evaporating at 80 °C for 45 min according to the ratio of material to liquid of 1:10, and the process was repeated three times. The water extract was then freeze-dried for 48 h to obtain C. tinctoria. The components of water extract in C. tinctoria were determined by liquid chromatography mass spectrometry (LC-MS) with TripleTOF5600+ (AB SCIEX™, Boston, MA, USA). Kaempferol (Purity ≥ 95%, HPLC grade) was purchased from Dalian Meilun Biotechnology Co., Ltd. (Dalian, China).

2.2. Animals and Experimental Design

This study was performed in accordance with protocols approved by the Animal Ethics Committee of Agricultural Product Quality Supervision, Inspection, and Testing Center (Beijing) of Ministry of Agriculture, China Agricultural University (KY19037, Beijing, China). Four-week-old male C57BL/6J mice (12–15 g) were purchased from Vital River Laboratory Technology Co., Ltd. (Beijing, China). Animals received sterile water and food ad libitum and were housed in standard plastic cages under a 12 h light/dark cycle at a controlled temperature (23 ± 2 °C). The 45% high-fat diet used in this experiment was purchased from Beijing HFK Bioscience Co., Ltd. (Beijing, China), and the normal diet was purchased from Beijing KEAO XIELI Feed Co., Ltd. (Beijing, China). Prior to the experiment, the mice were acclimated to the new environment for 1 week. Then, the diet-induced obesity (DIO) mice models (n = 32) were established by feeding the high-fat diet and the control check (CK, n = 8), which allowed access to the normal diet, until there were significant differences in body weight and blood glucose between DIO mice and CK mice at 10 weeks. After that, the DIO mice (n = 32) were randomly divided into four groups: the high-fat diet group (HFD, n = 8), the HFD+Kaempferol-Low group (KaeL, n = 8), the HFD+Kaempferol-High group (KaeH, n = 8), and the HFD+water extract of C. tinctoria group (Ct, n = 8). The KaeL group and KaeH group were administered kaempferol at concentrations of 25 mg/kg or 50 mg/kg (0.1 mL/10 g bodyweight) daily by oral gavage. Mice in the Ct group were treated with 0.4 g/mL water extract of C. tinctoria (0.1 mL/10 g bodyweight). CK and HFD groups were administered sterile water (0.1 mL/10 g bodyweight) daily by oral gavage. The mice were treated for eight weeks. During the treatment period, the animal behavior was observed daily, and body weight was measured weekly. Fasting blood glucose was measured at the 10th week, at the 12th week, at the 15th week, and at the 18th week. At the 18th week, mouse fecal samples were collected. Then, mice were anesthetized and euthanized by exsanguination, and blood samples and tissues were collected.

2.3. ITT

At the 16th week, mice were fasted for 4 h, and then an intraperitoneal insulin tolerance test (ITT) was performed after insulin injection (0.70 U per kg body weight). The tail blood was collected at 0 min, 15 min, 30 min, 45 min, and 60 min, and blood glucose was measured. The AUC for ITT was calculated by the trapezoidal rule.

2.4. GTT

At the 17th week, GTT was performed. Mice were fasted for 16 h, and then intraperitoneally (i.p.) injected with 1.5 g/kg body weight glucose. The blood glucose values of each mouse were measured at 0 min, 15 min, 30 min, 60 min, 90 min, and 120 min. The area under the curve (AUC) was given as the incremental AUC calculated by the conventional trapezoid rule.

2.5. Biochemical Analysis

High-density lipoprotein (HDL), low-density lipoprotein (LDL), triacylglycerols (TG), total cholesterol (TC), alkaline phosphatase (ALP), aspartate transaminase (AST), alanine aminotransferase (ALT), total protein (TP), albumin (ALB), uric acid (UA), creatinine (CREA), blood urea nitrogen (BUN) and glucose (GLU) in serum were determined using an automatic biochemical analyzer (Hitachi, 7600-020, Tokyo, Japan). Free fat acid (FFA) in the serum was measured with the kits of enzyme-linked immunosorbent assay according to the manufacturer’s recommendations (Nanjing Jiancheng Bioengineering Institute, Nanjing, China).

2.6. Hemoglobin A1c Analysis

In the last week of the experiment, mice were sacrificed and hemoglobin a1c (HbA1c) was measured in whole blood with glycosylated hemoglobin enzyme-linked immunosorbent assay kits (Beijing Sinouk Institute of Biological Technology, Beijing, China).

2.7. Gut Microbiota Analysis

Fresh mouse fecal samples were collected from all groups and immediately frozen at −80 °C in the last week. Fecal microbial genomic DNA was extracted using the Stool Genomic DNA Extraction Kit (Beijing Solarbio Technology Co., Ltd., Beijing, China) following the manufacturer’s protocol. Then, the V3–V4 hypervariable regions of 16S ribosomal DNA (rDNA) were amplified with High-Fidelity Polymerase and Phusion® High-Fidelity PCR Master Mix with GC Buffer using specific primers with barcode. Sequencing libraries were established by the TruSeq® DNA PCR-Free Sample Preparation Kit, and all samples were sequenced on the HiSeq2500 PE250 platform (Illumina, San Diego, CA, USA). Further processing of raw sequencing data was performed according to the Qiime quality control procedure (V1.7.0, http://qiime.org/scripts/split_libraries_fastq.html (accessed on 3 January 2020)). The lowest amount of data in the sample is used as the standard for normalization. Gut microbiota data analyses were performed by PAST3 software, Excel, Heatmap Illustrator1.0, and Huttenhower Lab Galaxy Server.

2.8. Statistical Analysis

Experimental data are presented as mean ± standard deviation (SD). The significant differences between groups were determined by one-way ANOVA with Tukey’s post hoc test. A difference was considered to be significant at p < 0.05. p values of less than 0.05, 0.01, 0.001, and 0.0001 are expressed as * p < 0.05 (vs. HFD group), ** p < 0.01 (vs. HFD group), *** p < 0.001, and **** p < 0.0001 (vs. HFD group), respectively. Graphing of the data was carried out using Graph Prism.

3. Results

3.1. Components of the Extract of C. tinctoria

As shown in Table 1, flavonoids are the main components of water extract in C. tinctoria, among them kaempferol, eriodictyol, luteolin, and quercetin-3-O-glucoside.

3.2. C. tinctoria and Kaempferol Reduced Body Weight and Improved Obesity in DIO Mice

To explore the effects of C. tinctoria and kaempferol on hyperglycemia in obese mice, an obese mouse model was successfully established by feeding HFD. After 10 weeks, the body weight and fasting blood glucose of the HFD (before treatment with C. tinctoria and kaempferol) were significantly elevated compared to those of the control group. During the administration of C. tinctoria, the weight of mice in the Ct group was lower than that in HFD group, although the difference was not significant (Figure 1a). Treatment with kaempferol also reduced the body weight gain; especially, the KaeH was more effective in ameliorating the increase in body weight. During the 18-week feeding, no significant difference in food intake was observed between the treatment group and the HFD group (Figure 1b). Similar results were observed in organ coefficients (Figure 1c). Furthermore, the fasting blood glucose of C. tinctoria group appeared to decrease at the 15th week and kaempferol groups reached a significant level at the 18th week (Figure 1d) (p < 0.0001). These results show that C. tinctoria and kaempferol effectively improved the obesity of hyperglycemic mice induced by HFD without affecting the food intake of DIO mice.

3.3. C. tinctoria and Kaempferol Ameliorated Glucose Metabolism in DIO Mice

In order to determine the hypoglycemic effects of C. tinctoria and kaempferol, GTTs and ITTs were performed at the 17th week and 16th week, respectively. The 16 h fasting blood glucose levels of the HFD group were significantly elevated compared to the CK group (p < 0.0001), and treatment with C. tinctoria and kaempferol significantly mitigated HFD-induced blood glucose elevation (Figure 2a,b) (p < 0.05). The results of GTTs show that C. tinctoria and kaempferol could effectively improve glucose tolerance of DIO mice. Significant differences were observed in insulin tolerance for the 4 h fasting blood glucose levels (Figure 2c,d). Insulin sensitivities of the HFD group were impaired compared to the CK group, but kaempferol significantly reversed the insulin resistance induced by high-fat diet. Based on the above results, C. tinctoria and kaempferol could effectively lower serum glucose and improve glucose intolerance and insulin resistance in DIO mice.
If HbA1c > 9% indicates that patients have persistent hyperglycemia, complications such as diabetic nephropathy, arteriosclerosis, and cataract will occur [21,22]. As shown in Figure 2e, kaempferol groups showed significantly lower concentrations of HbAc1 compared with HFD groups in DIO mice.

3.4. C. tinctoria and Kaempferol Improve Obesity without Effect on the Liver and Kidney in DIO Mice

The concentrations of serum TC, TG, HDL, LDL, and FFA in all groups were determined at 8 weeks of administration (Figure 3a–d,f). TC, HDL, and FFA levels were reversed in the HFD group after treatment with C. tinctoria and kaempferol, but no significant difference was observed. Moreover, kaempferol significantly decreased serum glucose levels in DIO mice compared to the HFD group (Figure 3e) (p < 0.01). In addition, no significant changes in liver or kidney function indicators were observed in the administration groups compared to the HFD groups (Figure 3g,h). These results indicate that C. tinctoria and kaempferol were capable of mitigating obesity progress, and had no effect on liver and kidney function parameters.

3.5. Effect of C. tinctoria and Kaempferol on Gut Microbe in DIO Mice

To evaluate the impact of C. tinctoria and kaempferol treatment on gut microbiota diversity, the α and β diversity of all groups were measured (Figure 4a,b). The α diversity had no significant difference, while the β diversity was significantly elevated after treatment with C. tinctoria and kaempferol compared to the HFD groups (p < 0.05). The analysis of nonmetric multidimensional scaling analysis (NMDS) showed that there was a significant difference in gut microbial composition between high-fat diet-induced obese hyperglycemic mice and normal diet mice (p < 0.01, Figure 4c). Administration of C. tinctoria and kaempferol had significant effects on the composition of intestinal flora in DIO mice and enabled the composition of HFD mice to migrate to that of CK mice.
As shown in Figure 4d, Firmicutes, proteus, Bacteroidetes, and actinomycetes were important components of the gut microbe, accounting for more than 90%, and there were also some TM7, desferribacilli, verruca, soft wall bacteria, and cyanobacteria in all groups. Compared with the CK group, Bacteroidetes in the HFD group decreased. After treatment with C. tinctoria and kaempferol, Bacteroidetes increased. Actinomycetes increased from 1.34% to 13.51% compared with CK to HFD. C. tinctoria and kaempferol treatment reduced Actinomycetes in high-fat diet mice. Similar improvements were observed for Bacteroidetes/Firmicutes (Figure 4e).
Heat map cluster analysis of gut microbiota was performed, and the results are illustrated in Figure 4f. As expected, there was a significant difference in intestinal flora between HFD and CK, represented as Dehalobacterium of the phylum Firmicutes decreasing significantly (p < 0.01), Desulfovibrio of the phylum Proteus decreasing significantly (p < 0.01), and collinella of the phylum actinobacteriaceae increasing significantly (p < 0.01). These changes were significantly reversed in Ct, KaeL, and KaeH groups (p < 0.01).
The results of LEfSe cluster analysis were consistent with those of NMDS analysis. There was a significant decrease in dehalobacterium (p < 0.05), Desulfovibrio (p < 0.05), s24-7 (muribaculaceae), and Collins (coriobacteriaeae) of actinobacteria (collinsella). The content of Bifidobacterium pseudolongum, allobaculum, and Bacillus cereus increased significantly (p < 0.05) compared with CK (Figure 5a,b). After treatment with C. tinctoria, the number of Vibrio butyricimonas (p < 0.01), dehalobacterium, anaerostipes, lachnospira, and Mycoplasma increased significantly (p < 0.05) compared with the HFD group (Figure 5c,d), while muciniphila of akkermansia and caccae of bacteroidea decreased significantly (p < 0.05) in KaeL (Figure 5e,f). Oscillospira (p < 0.05), schaedleri species (p < 0.05), dehalobacterium (p < 0.05), and Vibrio butyricimonas (p < 0.01) of Firmicutes increased significantly and Proteus flexispira and sutterella decreased significantly (p < 0.05) in KaeH (Figure 5g,h). Therefore, C. tinctoria and kaempferol treatment ameliorated the whole gut microbe in DIO mice.

4. Discussion

C. tinctoria has been used in tea and food for many years [13]. The beneficial effects of C. tinctoria mainly consist of anti-inflammatory and antioxidant effects, which are attributed to its flavonoids [23,24,25]. In addition, polysaccharides, phenylpropanoids, polyacetylenes, and other substances in C. tinctoria also have certain pharmacological activities [26,27,28]. However, these components have not attracted enough attention at present. Here, we verified that the extracts of C. tinctoria and its flavonoid kaempferol could reduce blood glucose and improve insulin sensitivity partly through regulating gut microbiota.
In this study, fasting blood glucose levels significantly decreased with kaempferol treatment in high-fat diet-induced obese mice, but there was no significant difference in the Ct group. It has been observed in cell and animal experiments that kaempferol can improve obesity by inhibiting adipogenesis [29,30].
In GTT and ITT experiments, both C. tinctoria and kaempferol significantly ameliorated glucose tolerance and insulin sensitivity compared with the HFD group. It has been reported that the extracts of C. tinctoria could significantly reduce blood glucose of diabetic mice [31]. Similar studies also showed that daily administration of kaempferol significantly decreased oral glucose tolerance, intraperitoneal insulin tolerance, and serum lipids [32].
In addition, C. tinctoria and kaempferol reduced TC, HDL, FFA, and glycosylated hemoglobin, and improved glucose metabolism and lipid metabolism in DIO mice. This is consistent with previous research results [33].
We also observed that the treatment of C. tinctoria and kaempferol had a significant effect on intestinal flora. Most obviously, the genus dehalobacterium of Firmicutes and Desulfovibrio of Proteus decreased significantly (p < 0.01), and collinella of actinomycetes increased significantly (p < 0.01) in HFD compared with CK, while C. tinctoria and kaempferol could significantly reverse the changes of these flora (p < 0.01). Previous research has shown that there is a correlation between collinella and insulin. The increase in Desulfovibrio can improve glucose metabolism, and the decrease in dehalobacterium will lead to premature aging, which is consistent with the results of collinella and Desulfovibrio regulating glucose metabolism in the literature [34,35,36]. The treatment of C. tinctoria and kaempferol can increase short-chain fatty acid-producing bacteria, such as butyrimionas (Vibrio butyricum), which is consistent with reports that short-chain fatty acids and other bioactive components can target intestines, liver, and other organs so as to improve intestinal health, control blood glucose, and regulate insulin resistance [37]. It was initially reported that obesity was associated with a lower proportion of Bacteroides than Firmicutes. However, this view was challenged by later studies [38].

5. Conclusions

In conclusion, C. tinctoria and its flavonoid kaempferol have protective effects on glucose metabolism disorder and changes in gut microbe in diet-induced obese mice. The alleviating effect may be related to the increase in bacteria regulating glucose metabolism and producing short-chain fatty acids.

Author Contributions

Conceptualization, F.Z. and M.Y.; methodology, J.X. and F.Z.; validation, Y.H. and M.Y.; resources, R.G.; data curation, Y.H., F.Z. and M.Y; writing—original draft preparation, F.Z. and M.Y.; writing—review and editing, R.G., K.H. and X.H. All authors have read and agreed to the published version of the manuscript.

Funding

K.L.H. and X.Y.H. would like to thank the 2115 Talent Development Program of China Agricultural University. This research was funded by the Science and Technology Project of Henan Province of P.R. China, grant number 202102310142.

Institutional Review Board Statement

The study was conducted according to the guidelines of the Declaration of Helsinki, and approved by the Animal Ethics Committee of Agricultural Product Quality Supervision, Inspection, and Testing Center (Beijing) of Ministry of Agriculture, China Agricultural University (protocol code KY19037, 9 August 2019).

Informed Consent Statement

Not applicable.

Data Availability Statement

Data are available from the corresponding author ([email protected]) upon reasonable request.

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. Effects of C. tinctoria and kaempferol on mouse physiology and glucose. (a) Weekly body weight of mice. (b) Mean daily food intake. (c) Organ coefficient. (d) Fasting blood glucose. Sub: subcutaneous fat, BAT: brown adipose tissue, Ep: epididymal fat, CK: control group, HFD: high-fat diet group, Ct: HFD+water extract of C. tinctoria group, KaeL: HFD+kaempferol low group, KaeH: HFD+kaempferol high group. Value = mean ± SD (n = 8). * p < 0.05 vs. HFD, ** p < 0.01 vs. HFD, *** p < 0.001 vs. HFD, **** p < 0.0001 vs. HFD.
Figure 1. Effects of C. tinctoria and kaempferol on mouse physiology and glucose. (a) Weekly body weight of mice. (b) Mean daily food intake. (c) Organ coefficient. (d) Fasting blood glucose. Sub: subcutaneous fat, BAT: brown adipose tissue, Ep: epididymal fat, CK: control group, HFD: high-fat diet group, Ct: HFD+water extract of C. tinctoria group, KaeL: HFD+kaempferol low group, KaeH: HFD+kaempferol high group. Value = mean ± SD (n = 8). * p < 0.05 vs. HFD, ** p < 0.01 vs. HFD, *** p < 0.001 vs. HFD, **** p < 0.0001 vs. HFD.
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Figure 2. Effects of C. tinctoria and kaempferol on glucose metabolism in DIO mice. (a) Glucose tolerance test (GTT). (b) The area under the curve (AUC) of GTT. (c) Insulin tolerance test (ITT). (d) The AUC of ITT. (e) Hemoglobin a1c (HbA1c) concentrations of whole blood. GHB: glycated hemoglobin, CK: control group, HFD: high-fat diet group, Ct: HFD+water extract of C. tinctoria group, KaeL: HFD+kaempferol low group, KaeH: HFD+kaempferol high group. Value = mean ± SD (n = 8). * p < 0.05 vs. HFD, ** p < 0.01 vs. HFD, **** p < 0.0001 vs. HFD.
Figure 2. Effects of C. tinctoria and kaempferol on glucose metabolism in DIO mice. (a) Glucose tolerance test (GTT). (b) The area under the curve (AUC) of GTT. (c) Insulin tolerance test (ITT). (d) The AUC of ITT. (e) Hemoglobin a1c (HbA1c) concentrations of whole blood. GHB: glycated hemoglobin, CK: control group, HFD: high-fat diet group, Ct: HFD+water extract of C. tinctoria group, KaeL: HFD+kaempferol low group, KaeH: HFD+kaempferol high group. Value = mean ± SD (n = 8). * p < 0.05 vs. HFD, ** p < 0.01 vs. HFD, **** p < 0.0001 vs. HFD.
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Figure 3. Effects of C. tinctoria and kaempferol on biochemical parameters of serum. (a) TC. (b) TG. (c) HDL. (d) LDL. (e) GLU. (f) FFA. (g) Liver function parameters. (h) Kidney function parameters. TC: total cholesterol, TG: triglyceride, HDL: high-density lipoprotein, LDL: low-density lipoprotein, GLU: glucose, FFA: free fatty acid, AST: aspartate transaminase, ALT: alanine aminotransferase, ALP: alkaline phosphatase, TP: total protein, ALB: albumin, CREA: creatinine, BUN: blood urea nitrogen, UA: uric acid, CK: control group, HFD: high-fat diet group, Ct: HFD+water extract of C. tinctoria group, KaeL: HFD+kaempferol low group, KaeH: HFD+kaempferol high group. Value = mean ± SD (n = 8). * p < 0.05 vs. HFD, ** p < 0.01 vs. HFD, **** p < 0.0001 vs. HFD.
Figure 3. Effects of C. tinctoria and kaempferol on biochemical parameters of serum. (a) TC. (b) TG. (c) HDL. (d) LDL. (e) GLU. (f) FFA. (g) Liver function parameters. (h) Kidney function parameters. TC: total cholesterol, TG: triglyceride, HDL: high-density lipoprotein, LDL: low-density lipoprotein, GLU: glucose, FFA: free fatty acid, AST: aspartate transaminase, ALT: alanine aminotransferase, ALP: alkaline phosphatase, TP: total protein, ALB: albumin, CREA: creatinine, BUN: blood urea nitrogen, UA: uric acid, CK: control group, HFD: high-fat diet group, Ct: HFD+water extract of C. tinctoria group, KaeL: HFD+kaempferol low group, KaeH: HFD+kaempferol high group. Value = mean ± SD (n = 8). * p < 0.05 vs. HFD, ** p < 0.01 vs. HFD, **** p < 0.0001 vs. HFD.
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Figure 4. Effect of C. tinctoria and kaempferol on gut microbe. (a) Simpson α diversity index among groups. (b) Bray-Curtis β diversity index among groups. (c) The NMDS graph shows the two-dimensional plane distribution of each group of animals (that is, the degree of difference between groups characterized by β diversity). (d) Microbial community analysis at the phylum level in mice. (e) The alteration in the Bacteroidetes to Firmicutes ratio in mice. (f) Heat map analysis of microbial community at the genus level in mice. CK: control group, HFD: high-fat diet group, Ct: HFD+water extract of C. tinctoria group, KaeL: HFD+kaempferol low group, KaeH: HFD+kaempferol high group. Value = mean ± SD (n = 8). * p < 0.05 vs. HFD, ** p < 0.01 vs. HFD, *** p < 0.001 vs. HFD, **** p < 0.0001 vs. HFD.
Figure 4. Effect of C. tinctoria and kaempferol on gut microbe. (a) Simpson α diversity index among groups. (b) Bray-Curtis β diversity index among groups. (c) The NMDS graph shows the two-dimensional plane distribution of each group of animals (that is, the degree of difference between groups characterized by β diversity). (d) Microbial community analysis at the phylum level in mice. (e) The alteration in the Bacteroidetes to Firmicutes ratio in mice. (f) Heat map analysis of microbial community at the genus level in mice. CK: control group, HFD: high-fat diet group, Ct: HFD+water extract of C. tinctoria group, KaeL: HFD+kaempferol low group, KaeH: HFD+kaempferol high group. Value = mean ± SD (n = 8). * p < 0.05 vs. HFD, ** p < 0.01 vs. HFD, *** p < 0.001 vs. HFD, **** p < 0.0001 vs. HFD.
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Figure 5. LEfSe cluster analysis of the structure of gut microbiome. Linear discriminant analysis effect size (LEfse) results are represented by circular cladograms (a,c,e,g). Differentially expressed taxa are highlighted by colored and shaded circles. The diameter of the circle is related to abundance of taxa. (a) CK vs. HFD; (c) Ct vs. HFD; (e) KaeL vs. HFD; (g) KaeH vs. HFD. Linear discriminant analysis (LDA) results are shown in figure (b,d,f,h). The length of the bar represents LDA score, and the colors of the bar represent the respective groups. The threshold on the logarithmic LDA score was set to 2.0. The taxon of bacteria with significant changes (p < 0.05) in relative abundance is written alongside the horizontal lines. (b) Red represents CK, green represents HFD; (d) red represents Ct, green represents HFD; (f) red represents HFD, green represents KaeL; (h) red represents HFD, green represents KaeH. CK: control group, HFD: high-fat diet group, Ct: HFD+water extract of C. tinctoria group, KaeL: HFD+kaempferol low group, KaeH: HFD+kaempferol high group.
Figure 5. LEfSe cluster analysis of the structure of gut microbiome. Linear discriminant analysis effect size (LEfse) results are represented by circular cladograms (a,c,e,g). Differentially expressed taxa are highlighted by colored and shaded circles. The diameter of the circle is related to abundance of taxa. (a) CK vs. HFD; (c) Ct vs. HFD; (e) KaeL vs. HFD; (g) KaeH vs. HFD. Linear discriminant analysis (LDA) results are shown in figure (b,d,f,h). The length of the bar represents LDA score, and the colors of the bar represent the respective groups. The threshold on the logarithmic LDA score was set to 2.0. The taxon of bacteria with significant changes (p < 0.05) in relative abundance is written alongside the horizontal lines. (b) Red represents CK, green represents HFD; (d) red represents Ct, green represents HFD; (f) red represents HFD, green represents KaeL; (h) red represents HFD, green represents KaeH. CK: control group, HFD: high-fat diet group, Ct: HFD+water extract of C. tinctoria group, KaeL: HFD+kaempferol low group, KaeH: HFD+kaempferol high group.
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Table
Table 1. Components of C. tinctoria.
Table 1. Components of C. tinctoria.
ComponentRetention Time (min)Peak Area (mV·min)Adduct Type
Eriodictyol4.574.42 × 107[M+H]+
Kaempferol5.048.54 × 106[M+H]+
Glycine-Betaine0.967.23 × 106[M+H]+
N-Fructosyl isoleucine1.787.02 × 106[M+H]+
Taxifolin4.622.94 × 106[M-H]-
Luteolin5.832.63 × 106[M+H]+
Anileridine6.322.04 × 106[M+H]+
3,5-Dicaffeoylquininic acid4.551.66 × 106[M-H]-
4-Methoxycinnamic acid6.031.66 × 106[M-H]-
Caffeoyl quinic acid3.371.46 × 106[M-H]-
Coumaric acid6.271.46 × 106[M+H-H2O]+
Quercetin-3-O-glucoside4.461.45 × 106[M+H]+
Eriodictyol-7-O-glucoside3.901.32 × 106[M+H]+
N,N-Dimethyldodecylamine N-oxide6.621.29 × 106[M+H]+
Luteolin-4’-O-glucoside4.901.24 × 106[M+H]+
Luteolin-7-O-glucoside4.331.03 × 106[M+H]+
isookanin-7-O-glucoside4.258.47 × 105[M-H]-
Naringenin6.377.43 × 105[M+H]+
Quercetin-3-O-glucoside; PlaSMA ID-12644.273.39 × 105[M-H]-
Caffeic acid4.063.28 × 105[M+H]+
Hyperoside4.932.70 × 105[M+H]+
Naringenin-7-O-glucoside5.162.66 × 105[M+H]+
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Zhang, F.; Yang, M.; Xu, J.; Hu, Y.; Gao, R.; Huang, K.; He, X. Coreopsis tinctoria and Its Flavonoids Ameliorate Hyperglycemia in Obese Mice Induced by High-Fat Diet. Nutrients 2022, 14, 1160. https://doi.org/10.3390/nu14061160

AMA Style

Zhang F, Yang M, Xu J, Hu Y, Gao R, Huang K, He X. Coreopsis tinctoria and Its Flavonoids Ameliorate Hyperglycemia in Obese Mice Induced by High-Fat Diet. Nutrients. 2022; 14(6):1160. https://doi.org/10.3390/nu14061160

Chicago/Turabian Style

Zhang, Feng, Minglan Yang, Jia Xu, Yanzhou Hu, Ruxin Gao, Kunlun Huang, and Xiaoyun He. 2022. "Coreopsis tinctoria and Its Flavonoids Ameliorate Hyperglycemia in Obese Mice Induced by High-Fat Diet" Nutrients 14, no. 6: 1160. https://doi.org/10.3390/nu14061160

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