Adipogenesis Inhibitory Activity of Hypersampsone P from Hypericum subsessile

Hui-Min Zhou 1,2 · Yan-Song Ye 1,2 · Na-Na Jiang 1,2 · Rong-Fang Mu 1,2 · Qian Wang 1,2 · Jing Hu 1 · Xia Liu 3 · Wan-Ying Qin 1,2 · Gang Xu 1,2 · Wen-Yong Xiong 1,2

Abstract

Keywords Adipogenesis · LKB1 · AMPK · Hypericum subsessile · Hypersampsone P

Graphic Abstract

1 Introduction

The overweight and obesity is an important origin for metabolic diseases, including high cholesterol, hyperlipidemia, diabetes and hypertension [ 1]. Prevalence of obesity and overweight has risen substantially in the past three decades, and more and more children became obese [ 2, 3]. The common therapies of obesity are surgery and pharmacotherapy [ 4]. Surgical treatment for severely obese patients has certain risks and postoperative side eあ ects [ 5]. The drugs for obesity treatment are also accompanied by cardiovascular disease, constipation, gastrointestinal adverse reactions and other side eあ ects while alleviating obesity [ 6, 7].

The obesity is mainly the result of over-nutrition on adipocyte tissue and the abnormal development of adipocytes [ 8], known as adipocyte diあ erentiation or adipogenesis, and the disease is related to unbalanced energy homeostasis [ 9]. Therefore, the regulation of adipogenesisis is signifi cant for obesity prevention and treatment [ 10]. Adipogenesis is regulated by complex network of transcription factors that coordinates the expression of many phenotypic proteins in adipocyte diあ erentiation [ 11]. Peroxisome proliferator activated receptor gamma (PPARγ) plays an essential role in white adipose tissue, which is involved in adipogenesis and lipid metabolism [ 12, 13]. And fatty acid binding protein 4 (FABP4) is a marker protein for adipocyte diあ erentiation, regulated by PPARγ [ 14]. These transcription factors regulators are regulated by multiple signaling pathways include AMPK signaling pathway. AMP-activated protein kinase (AMPK), a serine/threonine protein kinase that is widely expressed in eukaryotes [ 15], is a central regulator for obesity and energy homeostasis [ 16, 17]. AMPK is regulated by LKB1 (Liver kinase B1), which performs its biological functions through phosphorylation at sites such as S428 site [ 18]. In skeleton muscles, AMPK is activated in response to exercise and its activators has been proved as a potential target for obesity and T2DM [ 19, 20]. There is increasing evidence that AMPK inhibits the expression of PPAR and FABP4 and blunts adipogenesis in adipocytes [ 20- 22]. It was reported that Euphorbiasteroid blunted the diあ erentiation of human preadipocytes by enhancing the phosphorylation of AMPK for down-regulating PPARγ and fatty acid biosynthesis include sterol regulatory element-binding transcription factor 1 (SREBP1c), fatty acid synthase (FAS), acetyl-CoA carboxylase (ACC)α and stearoyl-CoA desaturase (SCD) [ 23]. Thus, natural products that aあ ect the AMPK signaling pathway may prevent obesity.

Polycyclic polyprenylated acylphloroglucinols (PPAPs) are characteristic secondary metabolites in the plants of Hypericum genus, yet the little is known for its bioactivities [ 24]. Only several PPAPs compounds from Hypericum patulum, has been showed inhibit T-type calcium channels [ 25]. Adamantane polycyclic polyprenylated acylphloroglucinols with caged architecture, a special class of hybrid natural products, is specifically rich in the plant family Guttiferae, especially Hypericum genus [ 26]. However, the bioactivity of Hypersampsone P, one of Adamantane PPAPs compounds extracted from Hypericum subsessile is still unknown [ 27]. Here we have screened a serial of PPAPs for their potential effects in adipocyte differentiation. Among the PPAPs, we identified the hypersampsone P shows a promising activity in regulating of adipogenesis and explored its potential mechanism in the effect. The result supported a novel function of the compound in regulation of adipocyte differentiation, indicating it is a potential candidate for treatment of obesity in near future.

2 Results

2.1 Screening the Eあ ects of PPAPs on Adipocyte Diあ erentiation

Here we have screened ten PPAPs by a classic cell model of adipocyte diあ erentiation (Fig. 1 a). Surprisingly, one of them (compounds 168) blunted the process of adipogenesis by measuring the changes of lipid content in the cells after fully inducing of adipogenesis (Fig. 1 b).

Then we choose three compounds, among the ten compounds, with the most similar chemical structure to insure the eあ ect with the unique structure for the bioactivity. As expected, compound 168 (hypersampsone P) was able to inhibit 3T3-L1 diあ erentiation to the degree as that of the positive control-LiCl, whereas higher concentrations of 169 (hypersampsone H) and 170 (hypersampsone M) did not aあ ect the process (Fig. 2 b, c). In combination with the chemical structures, the hydrogen on the 5-position carbon of compound 169 is chiral, and the 28-position carbon of compound 170 has geranyl group substitution (Fig. 2 a). The structure-activity relationships of these three compounds indicated that the hydrogen of 5-position carbon was necessary for the activity. Moreover, if there is the structure on the 28th site of geranyl group, the activity of hypersampsone P on adipogenesis can be reduced. These observations are meant to aid in the understanding of the administration of hypersampsone P in terms of its potential prevention or treatment of obesity.

These results support the eあ ect hypersampsone P on adipocyte diあ erentiation and the unique structure of the chirality of hydrogen on the fi fth site and the absence of geranyl group on the 28th site of hypersampsone P.

2.2 Hypersampsones P Inhibits Adipogenesis Dose-Dependently

We next elucidated the specifi city of hypersampsone P in regulation of the adipogenesis. Similarly, we treated cells with a series of concentrations in the range of 5-25 μM, and measured the lipid contents at the end of inducing adipogenesis. As shown, hypersampsone P blunted the lipid content in cells after inducing of the adipogenesis starting after 5 μM and almost reached a maxim inhibition about 20 μM (Fig. 3 a, b), supporting the eあ ect was dose-dependent (Fig. 3 c).

In consistent to the eあ ect above, the expressions of several diあ erentiation markers during adipogenesis, PPARγ and FABP4, were down-regulated, proving the eあ ect of hypersampsone P on adipogenesis (Fig. 3 d).

2.3 Hypersamsone P Blunts the Adipogenesis at the Early Stage

The adipocyte diあ erentiation is consist of several stages. To elucidate how hypersampsone P aあ ect the adipogenesis, we treated the cells at diあ erent stages of adipogenesis (Fig. 4 a) and measured the lipid content (Fig. 4 b). Not surprisingly, the maxim inhibition of hypersampsone P on the diあ erentiation were observed in the cells incubated by the compound at day 0-3, day0-5, or day 0-7, whereas the treatments at the day 3-5, day 3-7 or day 5-7 with hypersampsone P only inhibited the diあ erentiation mildly (Fig. 4 c), indicating hypersampsone P inhibits adipogenesis at the early stage of diあ erentiation.

2.4 Hypersampsone P Upregulated the LKB1-AMPK Signaling Pathway

During the early stage of adipocyte diあ erentiation, LKB1-AMPK signaling pathway plays a key role. Therefore we collected samples on the third day after induction and elucidated the phosphorylation of the LKB1 S428 . Interestingly, hypersampsone P did induce an increasing of the phosphorylation of LKB1 S428 (Fig. 5 a, b). Moreover, under the circumstances of the phosphorylation of AMPK T172 was blocked by an AMPK inhibitor-compound C, the upregulated AMPK phosphorylation by hypersampsone P was abolished, supporting that 20 μM hypersampsone P aあ ected the AMPK signaling pathway (Fig. 5 c, d). We detected the phosphorylation of the AMPK T172 treated by hypersampsone P (5-20 μM). It also up-regulated by hypersampsone P dose-dependently (Fig. 5 e, f). In addition, hypersampsone P down-regulated the gene expression of SREBP1c, ACCα, SCD1, FAS which all belong to the downstream of AMPK (Fig. 5 g-j).

3 Dissussion

In this study, we demonstrated the activity of hypersampsone P in adipocytes diあ erentiation. It indicated a potential development of the compound, as a new functional structure and a potential probe for exploring mechanism in chemistry biology.

First of all, we proposed the function of hypersampsone P in adipogenesis is most likely rely on the chirality of hydrogen on the fi fth site and the absence of geranyl group on the 28th site, because the other two compounds similar to hypersampsone P, hypersampsone H and hypersampsone M, did not aあ ect the process of adipogenesis (Fig. 2), providing an evidence of the unique structure of the compound on the eあ ect.

Regarding of the mechanism, our data demonstrated that hypersampsone P aあ ected the process of adipogenesis remarkably as long as we treated cells during the fi rst 3-day inducing of the diあ erentiation. Yet, the eあ ects were signifi cantly weaken if the diあ erentiation were treated by hypersampsone P after the 3-day inducing (Fig. 4). Furthermore, we hypothesis that hypersampsone P might aあ ect the LKB1, AMPK phosphorylation, along with the downstream SREBP1c, ACCα, SCD1, FAS’s gene expression during the early stage of the diあ erentiation (Fig. 5). LKB1 and AMPK are central sensors and regulators for cell metabolism and energy homeostasis. The eあ ect of hypersampsone P on LKB1-AMPK pathway highlights a reasonable mechanism for the eあ ect. However, lacking of enough amount of hypersampsone P limited our research in cell study only, in addition, how hypersampsone P targets to the LKB1-AMPK signaling pathway is still unknown.

Nevertheless, our results clearly demonstrated hypersampsone P’s function in regulation of adipocytes diあ erentiation, which is related to the overweight and obesity. It might be an alternative candidate as parent-structure for developing drug candidates for treatment of obesity in future.

4 Materials and Methods

4.1 3T3-L1 Culture and Diあ erentiation

3T3-L1 mouse preadipocytes were purchased from the American Type Culture Collection (ATCC, Manassas, VA, USA). Cells were cultured in DMEM supplemented with 10% CS. Two days after confl uence (day 0), cells were induced for diあ erentiation with DMEM supplemented with 10% FBS, IBMX, DEX and insulin (designated hereafter as MDI) as previously described [ 28]. On day 3, the medium was changed to medium containing 10% FBS and 1 μg/mL insulin for 2 days (day 5), and then insulin was removed from the 10% FBS-DMEM for another 2 days. The cells were fully diあ erentiated into mature adipocytes on day 7.

4.2 Oil Red O Staining

After removing the culture medium, 3T3-L1 cells were washed two times with PBS and subsequently fi xed in 10% formaldehyde overnight at room temperature. After fi xing, the cells were washed with water twice and one time with 60% isopropanol then the cells were stained with Oil Red O working solution for 10 min, washed with water, and then photos were taken under microscopy. To quantify lipids content, stained 3T3-L1 cells were washed with 100% isopropanol and the absorbance was measured at 492 nm by a microplate reader (Perkin Elmer Envision Multilabel reader). The absorbance in MDI group was standardized to 100%.

4.3 RNA Isolation and Real-Time PCR

RNA was extracted from 3T3-L1 cells using Trizol reagent (SANGONG BIOTECH), and cDNA was synthesized using cDNA synthesis kits using total RNA (2 μg) (Applied Biological Materials Inc). Real-time PCR cDNA gene expression was detected using the SYBR Green Master kit and a spectrofl uorometric thermal cycler (Applied Biosystems).

4.4 Western Blotting Analysis

Cells were washed twice with ice-cold PBS and subsequently lysed in equal volumes of cell lysis buあ er containing protein inhibitor cocktail (Sigma) for 30 min. Protein concentration was measured by BCA protein assay kit (Pierce). The lysates mixed with a certain amount of 5 × loading buあ er and boiled at 100 ℃ for 10 min. The protein was separated by 10% SDS-PAGE and transferred to PVDF membrane, blocked in 5% non-fat dried milk dissolved in PBS-T for 1 h and immunoblotted with antibodies specifi c for PPARγ, FABP4, t-AMPKα, P-AMPK T172 , t-ACC, P-ACC S79 and β-actin. Finally, the immunoblots were quantifi ed using the Metamorph software and expressed as a ratio of phosphorylated to total protein or total protein to β-actin.

Acknowledgements The work was supported by Yunnan Provincial Science and Technology Department, China (2017FA044), and Chongqing Municipal Natural Science Foundation (cstc2018jcyjAX0388).

Compliance with Ethical Standards

Conflict of interest The authors declare no competing fi nancial interest.

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