Abstract
Honokiol is a natural bioactive product with anti-tumor, anti-inflammatory, anti-oxidative, anti-angiogenic and neuroprotective properties. The present study aimed to investigate the effects of honokiol treatment on intimal thickening following vascular balloon injury. The current study determined that perivascular honokiol application reduced intimal thickening in rabbits 14 days after carotid artery injury, it may inhibit vascular smooth muscle cell (VSMCs) proliferation and reduce collagen deposition in local arteries. The findings of the presents study also suggested that honikiol may increase the mRNA expression levels of matrix metalloproteinase-1 (MMP-1), MMP-2 and MMP-9 and decrease tissue inhibitor of metalloproteinase-1 (TIMP-1) mRNA expression in the rabbit arteries. Additionally, perivascular honokiol application inhibited intimal thickening, possibly via inhibition of the phosphorylation of SMAD family member 2/3.
Keywords: honokiol, intimal thickening, vascular smooth muscle cells, matrix metalloproteinase, phosphorylated-Smad2/3
Introduction
Intimal hyperplasia contributes to the pathological process of several vascular disorders, including restenosis following angioplasty, transplant vasculopathy, vein graft stenosis and atherosclerosis (1). During vascular remodeling, vascular smooth muscle cells (VSMCs) proliferate, migrate and change from a contractile phenotype to a synthetic phenotype (2), inhibition of VSMC proliferation, migration and phenotypic modulation is a feasible treatment strategy to prevent intimal hyperplasia. The extracellular matrix (ECM) is composed of collagen subtypes and proteoglycans and has an important role in the process of intimal thickening. Collagen is the most abundant matrix protein in ECM, regulating collagen synthesis and degradation may also be a therapeutic target for intimal hyperplasia (3).
Honokiol (3′,5-di-(2-propenyl)-1,1′-biphenyl-2,4′-diol) (Fig. 1A) is a natural bioactive product obtained from plants in the genus Magnolia and has been determined to have multiple biological activities, including anti-cancer, anti-angiogenic, anti-inflammatory, anti-hypertensive, neuroprotective, anti-oxidative and anti-thrombosis properties (4–7). Honokiol has been shown to have the ability to protect endothelial cells and stimulate prostacyclin release in a rat carotid thrombosis model (6), which was revealed to have potential in preventing intimal hyperplasia (8,9). Lee et al determined that honokiol treatment inhibited VSMC growth by activating p38 mitogen activated protein kinase (10). A previous study suggested that honokiol may suppress tumor necrosis factor-a (TNF-α)-induced rat aortic smooth muscle cell proliferation via caspase and mitochondria-dependent apoptosis (11). These studies revealed that honokiol may have therapeutic potential in the prevention of vascular remodeling in cardiovascular diseases.
Figure 1.
(A) Chemical structure of honokiol. (B) Representative hematoxylin and eosin sections of injured arteries 14 days after balloon angioplasty. The distance between arrows indicated the intima area. Magnification, ×200. (C) Average intima area for the three treatment groups (n=8). ***P<0.001. (D) Average intima/media area ratios for the three treatment groups (n=8). ***P<0.001.
The present study investigated the effect of honokiol on intimal thickening following vascular balloon injury. Perivascular drug/gene delivery may effectively prevent intimal hyperplasia in preclinical experiments (12,13). Therefore, the present study hypothesized that perivascular honokiol application may inhibit neointimal hyperplasia in rabbits following carotid artery balloon injury through anti-proliferative ability. The present study investigated the effect of perivascular honokiol application on the expression of collagen, matrix metalloproteinases (MMPs), the tissue inhibitor of metalloproteinase-1 (TIMP-1) and the underlying mechanism involved in this process.
Materials and methods
Materials
F-127 pluronic gel was purchased from Sigma-Aldrich; Merck Millipore (Darmstadt, Germany). Honokiol was purchased from Selleck Chemicals (Houston, TX, USA). 3F Fogarty embolectomy catheters were obtained from Edwards Lifesciences (Irvine, CA, USA). The primer sequences used in mRNA analysis are presented in Table I. The primary antibodies used in western blotting analysis were: Smad2/3 (Santa Cruz Biotechnology, Inc., Dallas, TX, USA; catalog no. sc-6032), phosphorylated-Smad2/3 (p-Smad2/3; Santa Cruz Biotechnology, Inc.; catalog no. sc-11769), transforming growth factor-β1 (TGF-β1; Novus Biologicals, LLC, Littleton, CO, USA; catalog no. MAB240), TGF-β receptor type I (TGF-βRI; Santa Cruz Biotechnology, Inc.; catalog no. sc-398-G), TGF-βRII (Santa Cruz Biotechnology, Inc.; catalog no. sc-17792) and GAPDH (Abcam, Cambridge, UK; catalog no. ab8245). Mouse monoclonal α-smooth muscle actin (α-SMA; Abcam; catalog no. ab7817) and rabbit monoclonal anti-proliferating cell nuclear antigen (PCNA; Abcam; catalog no. ab19166) were used for immunohistochemistry analysis. The secondary antibodies were: Mouse anti-goat IgG horse radish peroxidase (HRP) (Santa Cruz Biotechnology, Inc.; catalog no. sc-2354) (for Smad2/3, p-Smad2/3, TGF-βRI), goat anti-mouse IgG HRP (Abcam; catalog no. ab205719) (for TGF-β1, TGF-βRII, GAPDH and a-SMA), goat anti-rabbit IgG HRP (Abcam; catalog no. ab205718) (for PCNA). Remaining solvents and reagents were analytical grade.
Table I.
Primer pairs used for quantitative polymerase chain reaction analysis in this study.
| Gene | Forward (5′-3′) | Reverse (5′-3′) |
|---|---|---|
| MMP-1 | AAAGGCCAGTATGCACAGCTTTC | TTCAACCACTGGGCCACTATTTC |
| MMP-2 | GAAGAGCGTGAAGGTTGGAA | TATCAGGTGGGGGTGAGAAG |
| MMP-9 | TGAGCTTTGACATCCTGCAC | TTTGTATCCGGCAAACTGGT |
| TIMP-1 | TTCTCATCGCTGGACAACTG | AGCGTAGGTCTTGGTGAAGC |
| GAPDH | GCACCGTCAAGGCTGAGAAC | TGGTGAAGACGCCAGTGGA |
MMP, matrix metalloproteinase; TIMP-1, tissue inhibitor of metalloproteinase-1.
Preparation of the honokiol-containing pluronic gel
F-127 pluronic gel (30% w/v) in saline was prepared and stored at −20°C for future use. Honokiol (10 mg) was dissolved in 1 ml dimethylsulphoxide (DMSO) and honokiol-containing pluronic gel was prepared by adding 1 ml of this solution to 9 ml of the previously prepared 30% pluronic gel at 4°C. Therefore, 1 ml of this solution contained 1 mg of honokiol. The resulting honokiol-containing pluronic gel was stored at −20°C for future use. It is of note that DMSO was used for the dilution because honokiol is insoluble in water and has a relatively poor solubility in ethanol.
Balloon endothelial denudation in rabbit carotid artery and perivascular honokiol application
Male New Zealand White rabbits (3.0–3.5 kg, n=24, aged 4–5 months) were obtained from the Laboratory Animal Center of The Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine (Shanghai, China), animals were housed at a temperature of 23±1°C and a humidity of 50±20% for 1 week with free access to food and water. General anesthesia was induced by intravenous injection of 3% pentobarbital sodium (1 ml/kg). A midline neck incision was made and the left carotid artery (left common carotid artery, left external carotid artery, left internal carotid artery) was exposed. Subsequently, a permanent ligature was made on the left external carotid artery ~5 mm away from the bifurcation, the left internal carotid artery was ligated by a bulldog clamp, another bulldog clamp was also placed on the proximal end of left common carotid artery. A 3F Fogarty embolectomy catheter was then introduced into the left common carotid artery through left external carotid artery to establish the animal model of vascular balloon injury. The balloon catheter was inflated with ~0.1 ml saline solution three times to denude the aorta endothelium, the length was about 3 cm. Immediately following balloon injury, 1 ml Pluronic gel containing honokiol or DMSO was applied around the injured carotid artery. Rabbits were randomly divided into three experimental groups: i) Honokiol treated group (1 mg, n=8); ii) vehicle (equal quantity of Pluronic gel containing DMSO) treated group (vehicle alone, n=8); and iii) untreated group (balloon injury without any treatment, n=8). The left external carotid artery was ligated immediately after treatment, the bulldog clamps were removed and the incision was closed. All animals recovered after 40–60 min surgery and showed no symptoms of stroke. Animals were euthanized and sacrificed in order to collect the carotid arteries 14 days post-surgery, three segments were cut from each artery, one segment was fixed in 10% buffered formalin and the remaining two segments were stored in liquid nitrogen. The protocols were approved by the Animal Care and Use Committee of Shanghai Jiao Tong University School of Medicine.
Histopathological staining and morphometry
Carotid arteries were fixed in formalin fixative solution for 24 h, then dehydrated in graded ethanol and subsequently embedded in paraffin. Transverse 5 µm slices were cut and then stained with hematoxylin and eosin (H&E) (3 min for hematoxylin and 30 sec for eosin at room temperature) and Masson (5–10 min at room temperature) following the manufacturer's protocol. The cross-sectional intima area, media area and intima-to-media (I/M) area ratio were calculated from the H&E stain slices, collagen fibers were calculated on Masson staining slices (photographed by a Nikon light microscope). All the data was analyzed and calculated using the Image-Pro Plus version 6.0 (Media Cybernetics, Inc., Rockville, MD, USA).
Immunohistochemistry staining
Paraffin-embedded tissues were cut into 5-µm thick slices, the sections were incubated with primary antibodies (α-SMA, 1:2,000 dilution; and PCNA, 1:2,000 dilution) at 4°C overnight and then stained with a labeled DAB Detection kit (Fuzhou Maixin Biotech Co., Ltd., Fuzhou, China), followed by counterstaining with hematoxylin (30 sec at room temperature). Negative control was treated with PBS. A total of 5 sections of each carotid artery were selected for quantification, and 4 random fields were imaged at magnification of ×200 in each section. The number of positively stained cells was quantified using Image-Pro PLUS version 6.0 (Media Cybernetics, Inc.).
Reverse transcription-quantitative polymerase chain reaction analysis (RT-qPCR)
TRIzol reagent (Molecular Research Center, Cincinnati, OH, USA) was used to isolate total RNA from the tissues according to the manufacturer's protocol. cDNA was synthesized from 1 µg of total RNA using iScript cDNA Synthesis kit (Bio-Rad Laboratories, Inc., Hercules, CA, USA) at 42°C for 60 min, 70°C for 10 min and 4°C for storage). qPCR was performed using SYBR Premix Ex Taq kit (Takara, Bio, Inc., Otsu, Japan) on a Stratagene Mx3005 RT-qPCR thermocycler (30 sec at 95°C, followed by 50 cycles of denaturation at 95°C for 5 sec, annealing step at 60°C for 35 sec and extension at 72°C for 15 sec). The mRNA expression levels of samples were measured using the 2−ΔΔCq method (14). The primer sequences used in the current study are presented in Table I.
Western blotting analysis
Carotid arteries were homogenized in radioimmunoprecipitation assay (RIPA) lysis buffer, the protein concentration was determined using Bicinchoninic acid Protein Assay reagent (Thermo Fisher Scientific, Inc., Waltham, MA, USA). Equal quantity protein lysates (30 µg) was separated by 10% sodium dodecyl sulfate-polyacrylamide gel electrophoresis and then transferred to polyvinylidene difluoride membrane (EMD Millipore, Billerica, MA, USA). Membranes were blocked with 5% non-fat milk for 1 h and subsequently incubated with primary antibodies (Smad2/3 1:1,000 dilution; p-Smad2/3 1:1,000 dilution; TGF-β1 1:1,000 dilution; TGF-βRI 1:200 dilution; TGF-βRII 1:200 dilution; GAPDH 1:1,000 dilution) at 4°C overnight, followed by incubation with a secondary antibody for 1 h (at room temperature, 1:200 dilution for all). Protein bands were detected with enhanced chemiluminescence. Protein bands were determined by Quantity One version 4.62 software (Bio-Rad Laboratories, Inc., Hercules, CA, USA), and each band was determined three times.
Statistical analysis
Data are presented as the mean ± standard deviation and were analyzed by one-way analysis of variance with the SPSS version 22.0.0.0 (IBM Corporation, Armonk, NY, USA). P<0.05 was considered to indicate statistically significant difference.
Results
Perivascular honokiol application inhibited intimal hyperplasia 14 days after vascular injury
H&E staining was used to assess the effect of honokiol on intimal thickening following vascular injury, as presented in Fig. 1B. Morphometric analysis of the three treatment groups revealed that the intima area was significantly reduced in the honokiol treatment group when compared with the vehicle and untreated groups (Fig. 1C), the I/M area ratios followed a similar pattern (Fig. 1C). No significant difference was identified between intimal area and I/M area ratios in the vehicle and the untreated groups. These findings suggested that honokiol was effective in inhibiting intimal thickening and the vehicle treatment had no effect on intimal hyperplasia.
Perivascular honokiol application reduced intimal VSMC proliferation 14 days after vascular injury
Immunohistochemistry staining for α-SMA and PCNA was performed to investigate whether honokiol reduced neointima formation by inhibiting proliferation of VSMCs. It was determined that the majority of neointimal cells were positive for α-SMA, indicating that the cells that proliferated in the intima were VSMCs (Fig. 2A). Additionally, intimal proliferation was observed with immunohistochemistry staining of PCNA (a marker for cell proliferation) and presented in Fig. 2B, the ratio of PCNA-positive cells was significantly reduced in the honokiol-treated group in comparison with vehicle and untreated groups (Fig. 2C). These findings indicated that local honokiol treatment significantly inhibited intimal VSMCs proliferation.
Figure 2.
Effect of perivascular honokiol application on intimal vascular smooth muscle cell proliferation. (A) Representative immunohistochemistry staining of α-smooth muscle actin 14 days after balloon angioplasty. The distance between the arrows indicates the intima area. Magnification, ×200. (B) Representative immunohistochemistry staining of PCNA 14 days after balloon angioplasty. The distance between the arrows indicates the intima area. Magnification, ×200. (C) Ratio of PCNA-positive nuclei to total cell nuclei in the intima area (n=8). ***P<0.001. PCNA, proliferating cell nuclear antigen.
Perivascular honokiol application reduced collagen deposition following vascular injury
Collagen contents in the arteries 14 days after vascular injury were assessed with Masson staining (Fig. 3A), as presented in Fig. 3B, honokiol treatment group had a significantly reduced the collagen content compared with the vehicle and untreated groups, the vehicle treatment group exhibited similar collagen deposition compared with the untreated group.
Figure 3.
Effect of perivascular honokiol application on collagen deposition. (A) Representative Masson staining sections of injured arteries 14 days after balloon angioplasty. The distance between the arrows indicated the intima area. Magnifications, ×200. (B) Masson's staining-positive area to total intimal area in the three injured groups (n=8). **P<0.01, ***P<0.001.
Effects of perivascular honokiol application on the expression of MMPs and TIMP-1
MMPs and TIMP-1 have essential roles in intimal thickening following vascular injury; therefore, the expression of MMPs and TIMP-1 was investigated using RT-qPCR analysis. As presented in Fig. 4, there was a significant increase in the MMP-1, MMP-2 and MMP-9 mRNA expression levels when the honokiol-treated group was compared with the vehicle and untreated groups. TIMP-1 mRNA expression was significantly reduced in the honokiol treated group compared with the vehicle and untreated groups. No significant difference was identified between the vehicle-treated group and untreated group in terms of the expression of MMPs and TIMP-1.
Figure 4.
Effects of perivascular honokiol application on the expression of MMPs and TIMP-1. (A) Reverse transcription-quantitative polymerase chain reaction analysis of (A) MMP-1, (B) MMP-2, (C) MMP-9 and (D) TIMP-1 mRNA expression, GAPDH was used as an internal standard (n=8). *P<0.05, **P<0.01, ***P<0.001. MMP-1,-2,-9, matrix metalloproteinase-1,-2,-9; TIMP-1, tissue inhibitor of metalloproteinase-1.
Perivascular honokiol application downregulated phosphorylation of Smad2/3 expression
TGF-β1/Smad2/3 signaling is a critical regulator in the pathological process of intimal hyperplasia and inhibition of the TGF-β1/Smad2/3 signaling pathway may reduce VSMC proliferation and collagen deposition, thus attenuating intimal hyperplasia (15–17). Therefore, the present study investigated whether the reduced VSMC proliferation and collagen deposition were mediated via TGF-β1/Smad2/3 pathway. It is of note that western blot analysis revealed that honokiol treatment significantly reduced the expression of p-Smad2/3, whereas TGF-β1 and Smad2/3 expression showed no obvious change in the honokiol treatment group compared with vehicle or untreated groups (Fig. 5). TGF-βRII phosphorylates TGF-βRI and then TGF-βRI in turn phosphorylates Smad2/3 (18); therefore, the expression of TGF-βRI and TGF-βRII was subsequently analyzed. However, no significant difference was identified between the honokiol, vehicle or untreated groups (Fig. 5).
Figure 5.
Effect of perivascular honokiol application on the expression of the TGF-β1/Smad2/3 signaling pathway. (A) Representative western blotting indicating the levels of Smad2/3, TGF-β1, p-Smad2/3, TGF-βRI and TGF-βRII. (B) Quantitative analysis of protein expression levels (n=8). ***P<0.001. Smad2/3, SMAD family member 2/3; p-Smad2/3, phosphorylated Smad2/3; TGF-β1, transforming growth factor-β1; TGF-βRI, TGF-β receptor type I; TGF-βII, TGF-β receptor type II.
Discussion
The present study demonstrated that perivascular honokiol treatment inhibited intimal hyperplasia in rabbits 14 days after carotid artery balloon injury. The findings also revealed that honokiol treatment reduced VSMC proliferation and collagen deposition in the arteries following vascular injury. Additionally, the mRNA expression levels of MMP-1, MMP-2 and MMP-9 were upregulated, whereas TIMP-1 was downregulated in the honokiol treatment group. Subsequently the underlying mechanism was investigated and it was revealed that honokiol treatment reduced the phosphorylation of Smad2/3.
The adventitia has been considered to be an important regulator in vascular diseases, including hypertension, atherosclerosis and restenosis (19). Perivascular drug delivery is an effective method to prevent intimal hyperplasia as it may obtain controlled release and reduce the risk of thrombosis (drug released into the inner wall of vessels can impair reendothelialization, which would increase the risk of thrombosis) (13,20). The present study has demonstrated that local application of honokiol around the injured carotid artery may inhibit intimal thickening.
VSMCs have an important function in intimal thickening, and inhibition of VSMC proliferation is a feasible method to prevent intimal hyperplasia (2). Collagen is the most abundant matrix protein in ECM, treatments reducing collagen deposition are also feasible options to inhibit intimal thickening (3). The present study identified that perivascular honokiol application may reduce VSMCs proliferation 14 days after vascular injury, which was consistent with previous studies in vitro (10,11). Collagen content was also reduced in the honokiol-treated group compared with vehicle and untreated groups (Fig. 3). Additionally, a previous study determined that honokiol was able to reduce collagen deposition in a renal fibrosis model (21), demonstrating a potential antifibrotic effect of honokiol on other diseases.
MMPs and TIMPs have important functions in intimal thickening, MMPs may reduce ECM components and promote VSMC migration/proliferation, whereas TIMP-1 inhibits MMPs activity (22–24). It has been previously reported that honokiol may suppress the expression of MMPs in other diseases, such as cancer (melanoma, non-melanoma, urinary bladder cancer and gastric cancer) (25,26) and arthritis (27,28). However, the current study identified increased MMP-1, MMP-2 and MMP-9 mRNA levels in the honokiol-treated group, whereas TIMP-1 mRNA expression was significantly lower compared with vehicle or untreated groups (Fig. 4), this suggested that honokiol may increase the expression of MMPs and reduce the expression of TIMP-1 in local arteries, one of the possible reasons for this phenomenon is the difference between the cell lines and animal models; however, the underlying mechanism remains to be elucidated.
TGF-β1/Smad2/3 signaling has a key role in intimal hyperplasia; therefore, inhibition of the TGF-β/Smad2/3 signaling pathway may reduce VSMCs proliferation and collagen deposition, thus attenuating intimal hyperplasia (15–17). It is of note that the present study determined that honokiol treatment downregulated the protein expression level of p-Smad2/3, whereas the level of TGF-β1 and total Smad2/3 remained constant. TGF-β receptors may phosphorylate Smad2/3 (17); therefore, the present study investigated the expression of TGF-βRI and TGF-βRII. The results revealed that TGF-βRI and TGF-βRII were not significantly altered in the honokiol-treatment group. The findings of the present study revealed that honokiol may attenuate intimal hyperplasia by suppressing the phosphorylation of Smad2/3. A previous study determined that a natural compound baicalein may block the phosphorylation of Smad2 and Smad3 in hypertrophic scar-derived fibroblasts; however, baicalein did not affect the expression of TGF-β1, Smad2/3, TGF-βRI and TGF-βRII, the previous study determined that underlying mechanism involved baicalein binding directly to the catalytic region of activin receptor-like kinase 5 (ALK5) to inhibit phosphorylation of Smad2 and Smad3 (29). It is possible that in the present study honokiol blocked the phosphorylation of Smad2/3 via a pathway that did not involve any change in TGF-β1/Smad2/3 signaling, similar to ALK5.
In summary, the present study revealed that perivascular honokiol application reduced intimal thickening through inhibiting VSMCs proliferation and reducing collagen deposition in rabbits 14 days after carotid artery injury. Therefore, honokiol may potentially in reduce intimal hyperplasia in the pathological process of vascular disorders. To the best of our knowledge, the current study is the first to determine that honikiol may increase the expression of MMP-1, MMP-2 and MMP-9 and reduce TIMP-1 expression in rabbit arteries. Additionally, perivascular honokiol application inhibited intimal thickening, most likely through inhibiting the phosphorylation of Smad2/3.
Acknowledgements
The present study was supported by the National Natural Science Foundation of China for extending financial support (project no. 81300092).
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