Nobiletin exhibits protective potential on inflammation and inhibits the activation of transcription factors nuclear factor-κB (NF-κB). However, its effects on the progression of endometriosis remain unsettled. The present study aimed to explore the in vivo alleviation of nobiletin on endometriosis and its mechanism of action. The mouse model of endometriosis was established and administered with nobiletin. The ectopic lesion size was measured and the hotplate test was performed to assess the amelioration of nobiletin on endometriosis. The expression of proliferation and angiogenesis relevant genes including proliferating cell nuclear antigen (PCNA), vascular endothelial growth factor (VEGF), and E-cadherin was measured by immunostaining and the mRNA expression of proinflammatory mediators including interleukin (IL)-6, IL-1β, tumor necrosis factor (TNF)-α, matrix metalloproteinases (MMP)-1, and MMP-3 was measured by RT-PCR. The change of NF-κB activity in endometriotic cells was evaluated by Western blotting and confirmed by luciferase assay. Administration of nobiletin significantly reduced lesions size and pain in endometriosis mice. Nobiletin significantly altered the expression of PCNA, VEGF, and E-cadherin in ectopic endometrium, as well as the levels of IL-6, IL-1β, TNF-α, MMP-1, and MMP-3. Nobiletin also showed remarkably impairment on the activation of NF-κB in promoting endometriotic cells, likely targeting on the activity of IκB kinases (IKKs). The present study provides the first evidence that nobiletin exerts protection on endometriosis via inhibition the activation of NF-κB, specifically on the activity of IκB kinases.
Endometriosis is defined as the presence of endometrial tissue outside the uterine cavity . It is one of the most common gynecological disorders, affecting up to 10% of reproductive-aged women who suffer from chronic pelvic pain, dysmenorrhea, dyspareunia, and subfertility [2,3]. New discoveries on the genetic and immune systems in the endometrium of women with endometriosis, and the secreted cytokines of endometriotic lesions have given insights into the pathogenesis of this disorder, providing the foundation for new treatments for disease-associated pain and infertility . It is widely accepted that local inflammation occurs in the peritoneal cavity of patients with endometriosis, which is characterized by the alteration of the immunologic components and inflammatory mediators in peritoneal fluid . A number of studies have shown that hormone such as gonadotropin-releasing hormone (GnRH) agonists and progestogens reduced endometriotic lesion development. Anti-inflammatory drugs including tumor necrosis factor (TNF)-α inhibitors, peroxisome proliferator-activated receptor-g (PPAR-g) agonists, and antibody against matrix metalloproteinases (anti-MMP) exert therapeutic effects on endometriosis [6–8]. Along with this, the presence of nuclear factor-κB (NF-κB) in human endometrium supports its role in the physiology and pathophysiology of endometrial cells (ECs). Studies on the effects of NF-κB inhibitors in ECs and promoting endometriotic cells (EcCs) have shown that the inhibition of NF-κB could reduce endometriosis development and maintenance . Aberrant cytokine levels in the peritoneal fluid, which is regulated by NF-κB pathway, result in a proinflammatory local environment, promoting survival and growth of EcC in endometriosis patients . NF-κB is a transcriptional factor that plays a crucial role in inflammation, immunity, cell adhesion, invasion, cellular proliferation, apoptosis, and angiogenesis . Usage of NF-κB inhibitory agents in experimental endometriosis models has highlighted the role of the NF-κB pathway in endometriosis initiation and progression, making this pathway to be an attractive target for the treatment and prevention of endometriosis.
Flavonoids have been reported to be functioned as anti-inflammatory agent and certain flavonoids affect stress/cytokine-induced NF-κB signal transduction. Among them, nobiletin is a polymethoxylated flavonoid found in citrus fruit peel and has been widely used as herb medicine for centuries, playing important roles in tumor suppression, immune stimulation, anti-inflammation, antioxidation, as well as some cardiovascular disease mitigation [11,12]. For example, nobiletin inhibits the expression of the allergic cytokines, interleukin (IL)-4 and TNF-α as well as the activation of their transcription factors NF-κB . Given the inhibition of nobiletin on the NF-κB signaling which plays important roles in endometriosis pathogenesis, the objective of the present study was to investigate the effects of nobiletin on the development of endometriotic lesions and how the process is regulated by NF-κB in an in vivo experimental mice model of endometriosis.
Materials and methods
All animal procedures for these experiments were approved by the Institutional Animal and Use Committee at Liaocheng People’s Hospital. All mice were housed within environmentally controlled temperature and at a 12/12 h (light/dark) schedule. All procedures were conducted in accordance with the approved animal protocol.
Nobiletin was isolated from Citrus depressa as described  and dissolved in saline containing 0.5% (v/v) Tween 80 (Sigma-Aldrich, PA, U.S.A.). The following primary antibodies were used: Primary antibodies used in immunohistochemistry against proliferating cell nuclear antigen (PCNA), vascular endothelial growth factor (VEGF), and E-cadherin were purchased from Santa Cruz Biotechnology (Santa Cruz, CA, U.S.A.). Rabbit monoclonal antibodies used in Western blotting against IκB kinase (IKK)α, p-IKKα, IκBα, p-IκBα, β-actin, and Lamin B were purchased from Abcam (Cambridge, MA, U.S.A.). Rabbit monoclonal antibody against p65 was purchased from Beyotime (AN365, Jiangsu, China). The horseradish peroxidase-conjugated secondary antibodies were purchased from Thermofisher Scientific (Rockville, MD, U.S.A.).
Establishment of mouse model with endometriosis
Endometriosis was experimentally induced as previously described . Briefly, C57BL/6 female mice at 3–4 weeks were injected subcutaneously with pregnant mare serum gonadotropin (PMSG, 2 IU per mouse; Sigma-Aldrich). Approximately 42–44 h post PMSG injection, uteri tissues were harvested from these donor mice. Uterine stroma and epithelium (endometrium) were carefully separated from myometrium under dissecting microscope and were cut into 1 mm3 pieces. Further, endometrial pieces were suspended in saline, and 400 µl of suspension was injected into the peritoneal cavity of the recipient mice at 8–10 weeks. Recipient mice (2- to 4-month-old wild-type C57BL/6 immunocompetent, reproductively intact females) were anesthetized with ketamine/xylazine (87.5 and 12.5 mg/kg body weight), and Carprofen (5 mg/kg body weight) was given as analgesic upon surgery conclusion immediately and 48 h post-operatively. According to our preliminary study, after the establishment of endometriosis, the animals were divided randomly into four groups (n=12): Sham control group, endometriosis (EM) group, EM plus nobiletin at 10 and 20 mg/kg groups. In the treatment group, mice were administered nobiletin intraperitoneally daily for 28 consecutive days, and then killed through cervical dislocation and the total surface area of ectopic lesions in each mouse was evaluated. Specifically, the abdominal cavity was immediately reopened, and all lesions were measured with two perpendicular diameters (the length D1 and the width D2). The surface area of each endometrial implant tissue was calculated by the formula: S = π × D1 × D2/4 (in mm2).
The sensitivity of the nociception was evaluated by the hotplate test  with a commercially available Hot Plate Analgesia Meter (Model BME-480, Tianjin, China) consisting of a metal plate of 25 × 25 cm in size, which can be heated to a constant temperature of 54.0 + 0.1°C. As described in the manufacture’s instruction, the latency to respond to thermal stimulus is defined to be the time length (in second) elapsed from the moment when the mouse was placed in the cylinder to the time when it licked hind paws or jumped off the hot plate. The latency was calculated as the mean of two readings recorded at intervals of 24 h. To assess the time-course progression in thermal latency as a result of induced endometriosis, mice went through hotplate procedure at day 3, 7, 14, 21, and 28 respectively.
Mice ectopic lesions were fixed with 10% neutral buffered formalin for 24 h at room temperature, followed by immersion in 70% ethanol overnight at 4°C, then embedded in paraffin and sectioned at 4-μm thickness. For each paraffin-embedded tissue block, slide was stained by hematoxylin and eosin (H&E) and immunostained for different antibodies. For antigen retrieval, the slides were heated at 98°C in the EDTA buffer (pH 8.0) or the citric acid solution (pH 6.0) for a total of 30 min and cooled naturally at room temperature. The slides were incubated with primary antibodies against PCNA, VEGF, and E-cadherin, diluted to 1:2,000, 1:50, and 1:100 respectively at 4°C for 12 h. Further, after sufficient PBS wash, the slides were incubated with HRP-conjugated goat polyclonal antibody. The number and intensity of positive cells were counted by Image Pro-Plus 6.0 (Media Cybernetics, Inc., MD, U.S.A.). Images were obtained with the microscope fitted with a digital camera (Olympus, SD, U.S.A.).
Quantitative real-time polymerase chain reaction (qRT-PCR)
Ectopic endometrial samples were collected from the pelvic lesion region, and mRNA was extracted with RNeasy Mini Kit (Qiagen, Germany) according to manufacturer’s instruction. Concentration and quality of total RNA were assessed with a NanoDrop 2000 spectrophotometer (ThermoFisher Scientific, DE, U.S.A.). RNA was reverse transcribed using cDNA synthesis kits (Takara, Dalian, China), the expression levels of IL-6, IL-1β, TNF-α, MMP-1, and MMP-3 were determined using Taqman Real-Time PCR assays (Thermofisher Scientific) on CFX96 Touch™ Real-Time PCR Detection System (Bio-Rad, CA, U.S.A.). The designed primers were as follows: β-actin, F: 5′-CTGGGACGACATGGAGAAAA-3′, R: 5′-AAGGAAGGCTGGAAGAGTGC-3′; TNF-α, F: 5′-GCCACCACGCTCTTCTGTC-3′, R: 5′-TGCTCCTCCACTTGGTGGTT-3′; IL-1β, F: 5′-TTGACGGACCCCAAAAGATG-3′, R: 5′-AGCTGCCACAGCTTCTCCAC-3′; IL-6, F: 5′-CCATCCAGTTGCCTTCTTGG-3′, R: 5′-TGCAAGTGCATCATCGTTGT-3′; MMP-1, F: 5′-GGACTCTGAGCTCTTCTACC-3′; R: 5′-CACTAGAGACAAGAGTGGC-3′; MMP-3, F: 5′-GGCAGAACCAAACAGGAGC-3′, R: 5′- GGCCCAGGAGTGCCTTCCCTCC-3′.
Cell culture and treatment
Endometrial and endometriotic stromal cells were isolated and characterized according to previous studies . Briefly, minced tissues were digested with type IV collagenase (Millipore, Shanghai, China), and stromal cells were separated from epithelial glands by passing through nylon meshes. The obtained stromal cells were then cultured in Dulbecco Modified Eagle Medium (Gibco, MD, U.S.A.) supplemented with 10% fetal bovine serum (FBS) and antibiotics at 37°C.
The endometrial stromal cells were lysed and protein concentrations were determined by the Bradford method (Thermofisher Scientific, Gaithersburg, MD). Twenty-five micrograms of protein was loaded on 8% SDS-PAGE and transferred onto a polyvinylidene difluoride membrane (Millipore, Bedford, MA). Nonspecific binding was blocked in 5% nonfat milk at 4°C overnight. Membrane was then incubated with rabbit monoclonal antibodies against IKKα, p-IKKα, IκBα, p-IκBα, β-actin, P65, and Lamin B at a 1:1000 dilution for 1 h at 37°C. After washing with PBST buffer for three times, membrane was further incubated with HRP-conjugated second antibody at a 1:25,000 dilutions for 1 h at room temperature and detected by ECL substrate (Pierce, Rockville, MD).
The HEK293 cells (2 × 105) were seeded on 24-well plates (Corning, Shanghai, China) and transfected with p65 or IKKβ expression plasmids by standard calcium phosphate precipitation. After 34 h of transfection, cells were incubated with nobiletin of 10 and 20 µg/ml for 2 h respectively. Then, cells were harvested for luciferase assays. Luciferase assays were performed with a dual-specific luciferase assay kit (Promega, Durham, NC).
The comparison of distributions of continuous variables between or among two or more groups was made using the t-test, as well as one-way and two-way ANOVA respectively. P-values less than 0.05 were considered statistically significant. All data were analyzed with GraphPad Prism 5.0 software (GraphPad, San Diego, CA, U.S.A.).
Nobiletin reduced lesion size and hotplate latency in endometriosis mouse
As shown in Figure 1A, we found nobiletin reduced lesion size dose dependently in endometriosis mouse. Specifically, the volume of the lesion in the endometriosis group is approximately 60 mm2, while the endometriosis mice treated with 10 mg/kg per day had lesion size down to 30 mm2, and even lower size of 20 mm2 in the endometriosis mice treated with 20 mg/kg per day. In fact, low- and high- dose of nobiletin treatment resulted in average of 50 and 67% reduction in lesion size respectively (P<0.01).
Nobiletin reduced lesions size and pain in endometriosis mouse
We also assessed hotplate responses of mice from 3 days prior to the surgical induction of endometriosis or sham surgery until 4 weeks after the surgery with nobiletin treatment (Figure 1B). There were no differences in hotplate latency among all groups prior to the surgery, indicating the matched selection of mice in the experiment. However, starting from 3 days after surgery, the hotplate latencies decreased in all four groups due to the surgical trauma and adhesion, and the hotplate latencies in endometriosis groups were significantly lower than the one in the Sham surgery (no endometriosis). This trend has been kept to 7 weeks after the surgery. Of note, nobiletin treatment at both low- and high- doses significantly recovered the hotplate latency compared with the endometriosis mice without treatment, indicating the pain reduce in treated groups.
Effects of nobiletin on PCNA, VEGF, and E-cadherin immunochemistry in ectopic endometrium in endometriosis mouse
Figure 2A shows the PCNA, VEGF, and E-cadherin immunostaining in ectopic endometrium in mice with endometriosis. It can be seen that the staining levels of PCNA, VEGF, and E-cadherin vary significantly among different groups (Figure 2B). In particular, mice treated with nobiletin had significantly lower immunostaining to PCNA and VEGF in both low- and high-dose of nobiletin treated groups (P<0.01), and higher staining level of E-cadherin in nobiletin treated group, as compared with the untreated mice (P<0.01).
Effects of nobiletin on the expression of proliferation and angiogenesis relevant genes in ectopic endometrium
Inhibition of nobiletin on inflammatory responses in endometriosis mouse
As indicated in Figure 3A–E, the mRNA levels of IL-6, IL-1β, TNF-α, MMP-1, and MMP-3 in different treatment groups were evaluated by RT-PCR. Compared with the sham group, the expression levels of all these inflammatory factors were significant elevated in the endometriosis mice, suggesting the inflammation caused by the surgery. As expected, the treatment with nobiletin at 10 mg/kg/day decreased the levels of IL-6, IL-1β, and MMP-3 by 41, 30 and 33% respectively (P<0.01) and reduced the levels of TNF-α and MMP-1 by 18 and 24% respectively (P<0.05). Consistently, the treatment with nobiletin at 20 mg/kg/day reduced the levels of IL-6, IL-1β, TNF-α, MMP-1, and MMP-3 by 57, 66, 21, 30 and 47% respectively<0.01).
Effects of nobiletin on inflammatory responses in endometriosis mouse
Impact of nobiletin on NF-κB pathway activation
To examine whether NF-κB pathway is involved in the antagonism of nobiletin on endometriosis, IKKα/β activation and IκBα phosphorylation were evaluated by immunoblotting after stimulation by IL-1β. NF-κB complex (p50 and p65), which is associated with IκB to retain in the cytosol under resting state, is released and translocates to the nucleus . Therefore, we first investigated the time-course of IκBα phosphorylation in promoting endometriotic cells. Cells were treated by IL-1β (10 ng/ml) for 5 and 30 min and total proteins were extracted for Western blotting detection. The results showed that treatment with IL-1β enhanced the phosphorylation of IKKα and IκBα time dependently in human endometrial cells (Figure 4A–C). The phosphorylation of nuclear extract (p65) is also enhanced by IL-1β stimulation. With the treatment of nobiletin, the phosphorylation of these factors was reduced significantly at 30 min. Since p65 subunit is responsible for the transcriptional activity of NF-κB , we also determined the p65 nuclear accumulation. As illustrated in Figure 4D, nobiletin was able to inhibit the levels of p65 in time-dependent manner.
Activation of NF-κB is impaired in ESCs in response to different nobiletin concentration
Suppression of nobiletin on IKK-mediated activation of NF-κB pathway
To detect the effects of nobiletin on NF-κB dependent gene expression, HEK293 cells were transiently transfected with p65 and IKKβ promoter-dependent luciferase reporter construct. Treatment with nobiletin did not show change on p65 expression levels (Figure 5A), while the expression of IKKβ was repressed by pretreatment of nobiletin at low- and high-doses with comparing with control (Figure 5B).
Nobiletin inhibited the activity of IKKs but did not inhibit p65
Endometriosis was first described by Daniel Shroen in 1690  and is considered to be an inflammation type. Immune and inflammatory reactions at the cellular and molecular levels in endometriosis could contribute to the endometriotic implant survival and growth, and thus cause chronic pain and affect fertility . The NF-κB system dysfunction indicated by the molecular alterations of IL-6 and RelA (p65) during the late secretory phase in eutopic endometrium from endometriosis patients suggested that NF-κB could be an important factor in endometriosis etiology .
Nobiletin is polymethoxy flavonoid that is abundant in the pericarp of Citrus. Nobiletin exhibits various biological activities, including anti-inflammatory and antioxidative effects. Citrus aurantium extract, which is rich in nobiletin has been reported to activate lipid metabolism related genes, thus ameliorating ethanol-induced liver injury in mice . Nobiletin attenuates lipopolysaccharide/D galactosamine induced mouse model partly by inhibiting cytokine production mediated by NF-κB . Nobiletin ameliorate scratching in histamine induced mice by inhibited vascular permeability, the expression of IL-4 and TNF-α as well as the activation of NF-κB . To our knowledge, there are no published data on the treatment of nobiletin in the case of endometriosis. To explore the medical usage of nobiletin and better understand the mechanisms underlying the alleviation of endometriosis by nobiletin, we administrated nobiletin in mouse model with endometriosis and the expression of the relevant inflammatory factors and the activation of the NF-κB pathway were evaluated as compared with controls.
It is well accepted that endometriotic lesions require new blood supply to survive under the hypoxic environment of ectopic sites, therefore angiogenesis is essential for the development and progression of endometriosis . VEGF expression has been reported to be elevated in the eutopic glandular epithelium and peritoneal fluid of women with endometriosis during the late secretory phase [26,27]. In our study, we found nobiletin reduced lesion size in dose-dependent manner in endometriosis mouse, and we further detected how nobiletin affects the angiogenic ability with the endometriotic lesions. Compared with the untreated endometriosis mice, treatment with nobiletin significantly lowered PCNA and VEGF immunostaining, and showed higher staining level of E-cadherin in both low- and high-dose of nobiletin treated groups (P<0.01). The expression of several angiogenic factors is regulated by NF-κB, for instance, macrophages have been reported to produce VEGF under the control of NF-κB activation . It is therefore possible that nobiletin inhibited neoangiogenesis in endometriosis is a NF-κB -dependent process.
NF-κB is a transcription factor involved in numerous pathologies and known to be a proinflammatory, mitogenic, and antiapoptotic factor in many cell types . Its function was recognized in tumor necrosis factor and IL-1β receptors signaling pathways in several cell types . Human endometrial cells have been shown to express NF-κB proteins [29,30] and to activate NF-κB in response to IL-1β . Altered expression of proinflammatory cytokines in the endometrium has been shown to be associated with female fertility reduction and abortion dysregulation [32,33]. It has been suggested that the level of IL-6 in serum and TNF-α in peritoneal fluid could be used as markers to discriminate patients with endometriosis from others [34,,35]. Our results showed that the treatment with nobiletin significantly decreased the gene expression levels of IL-6, IL-1β and MMP-3 (P<0.01), TNF-α and MMP-1 (P<0.05). Due to the important participation of these factors in the pathophysiology of endometriosis, nobiletin could contribute to suppress the establishment and proliferation of ectopic endometrial implants.
NF-κB is composed of homodimers and heterodimers of five members including p65 (RelA), p105/p50, p100/p52, RelB, and c-Rel. The classic form of NF-κB is the heterodimer of the p50 and p65 subunits . In response to multiple stimuli, the IKKs complex binds with the regulatory subunit IKKγ/NF-κB essential modulator, which subsequently forms the TNF-α receptor complex and promotes IκB phosphorylation. Phosphorylated IκBα is rapidly ubiquitinated and degraded via a proteasome pathway. Degradation of IκBα leads to the expression of NF-κB, which translocates into the nucleus where it binds to specific binding sites within the promoter regions of target genes .
Chemotherapy agents or acute stimuli such as TNF-α, LPS, or PMA lead to the activation of IKKs which in turn phosphorylate two key serine residues, Ser32 and Ser36, on IκBs within the N-terminal response domain . These products are involved in the initiation, maintenance, and progression of endometriosis by inducing endometrial fragment adhesion, proliferation, and neovascularization . The immunocytochemical analysis in cultured epithelial endometrial cells revealed that the staining intensity of p65 was low during the proliferative phase, but increased during the secretory phase and was maximal at the time of implantation . In the present study, we investigated the time-course of IκBa phosphorylation in IL-1β mediated endometriotic cells, and our results showed that the phosphorylation of IKKα, IκBα, and p65 was reduced significantly at 30 min by nobiletin treatment. Further, to detect the effect of nobiletin on NF-κB dependent gene expression, p65 and IKKβ promoter-dependent luciferase reporter constructs were transfected into HEK293 cells, and we found nobiletin repressed the expression of IKKβ rather than p65, suggesting that IKK activation but not NF-κB complex.
To this end, we tested the effects of nobiletin on the development of endometriosis induced in mice and found that nobiletin decreased lesion sizes and pain in the animals. Further, we found that this alleviation was realized through the down-regulation of NF-κB signaling pathway and supported the reduction of the angiogenic and inflammatory gene expression, as well as the NF-κB complex activation.
The present study provides the first evidence that nobiletin exerts protection on endometriosis via inhibition the activation of NF-κB, specifically on the activity of IκB kinases.
Xin Wei and Xu Shao performed the experiments, analyzed, and interpreted the data. Xin Wei and Xu Shao wrote the manuscript. All authors read and approved the final manuscript.
The authors declare that there are no competing interests associated with the manuscript.
The authors confirm that there are no sources of funding to be acknowledged
hematoxylin and eosin
proliferating cell nuclear antigen
pregnant mare serum gonadotropin
quantitative real-time polymerase chain reaction
tumor necrosis factor
vascular endothelial growth factor