Atherosclerosis is the most frequently occurring form of arteriosclerosis, and it can lead to severe diseases such as myocardial infarction and cerebral infarction. During the development of atherosclerosis, low-density lipoprotein (LDL) first enters into the intima of blood vessels that have been damaged by high blood pressure and/or hyperglycemia and becomes oxidized. Monocytes then infiltrate the endothelium and differentiate into macrophages. When macrophages mainly absorb large quantities of oxidized LDL, they become foam cells, forming atheromas and inducing local inflammation1,2. Atheromas contain senescent cells (SCs) and are thought to be related to atherogenesis, which is associated with the progression of atherosclerosis3. SCs cannot divide, due to arrest of the G1/S phase checkpoint. The cyclin-dependent kinase (CDK) inhibitors p16INK4a and p21 promote cellular senescence and play a role specifically in vascular EC senescence4,5. Senescence-associated secretion phenotype (SASP) factors such as inflammatory cytokines are secreted by SCs and act on healthy peripheral tissues6,7. These findings indicate that SCs are involved in the biological alterations that accompany aging and many age-related diseases, including arteriosclerosis8,9,10. Recent studies using LDL receptor-deficient mice (Ldlr−/− mice) as a model of atherosclerosis showed that the selective removal of active foam cells expressing senescence-associated β-galactosidase (SA-β-Gal) using the Bcl-2 family protein inhibitor ABT-263 perturbs the proatherogenic environament11.

Molecular hydrogen (H2) reduces highly reactive oxygen species (ROS) including the hydroxyl radical and peroxynitrite, and functions as an antioxidant and anti-inflammatory agent12. The routes of H2 administration in animal models and human clinical studies are roughly classified into three types: inhalation of H2 gas, drinking H2-rich water (HW), and injection of H2-dissolved saline13. Inhalation of H2 gas ameliorates acute diseases such as ischemia-reperfusion injury and graft injury in several organs. Injecting H2-dissolved saline is as effective against ischemia-reperfusion injury as the inhalation of H2 gas13,14. Although drinking HW, the most convenient method of H2 administration, results in lower H2 concentrations in the blood than inhalation of H2 gas, it can be more effective at reducing oxidative stress and inflammation13. For example, drinking HW ameliorated symptoms of Parkinson’s disease in a rat model, whereas both H2 gas inhalation and lactulose-induced production of intestinal H2 did not15. We recently reported that pre-administration of HW was sufficient to attenuate septic inflammation in mice, strongly indicating that the therapeutic effects of HW derive from a mechanism distinct from the direct reduction of ROS by H216.

In our previous study, H2 administration prevented arteriosclerosis in apolipoprotein E-deficient (Apoe−/−) mice, a model of spontaneous atherosclerosis development17, suggesting that H2 administration suppresses vascular aging. Here, we examined whether drinking HW affects cellular senescence in atherosclerosis using Ldlr−/− mice.


Drinking HW decreased senescence markers in Ldlr −/− mice fed a high-fat diet

To induce SCs in atheromas, Ldlr−/− mice on a B6.129S7-Ldlrtm1Her/J background were fed a high-fat diet (HFD) consisting of 36% calories from fat. To determine whether drinking HW eliminates SCs, age-matched, 10-week-old Ldlr−/− mice were randomly divided into five groups: 1) regular chow diet (control diet) with control water; 2) control diet with HW; 3) HFD with control water; 4) HFD with HW; and 5) HFD with ABT-263, which was used as a positive control. Age-matched C57BL/6 J mice were fed a control diet and provided control water in the same facility over the same time period, as an additional control. All mice were sacrificed at 13 weeks from the start of the experiment. Immunohistochemical staining of the ascending aorta with antibodies against the senescence markers p16INK4a and p21 was performed to determine whether HW ameliorates HFD-induced cellular senescence in Ldlr−/− mice. As previously reported, p16INK4a and p21 were expressed in CD31-positive endothelial cells (ECs) in atheromas in HFD-fed Ldlr−/− mice (Fig. 1a,b). Monoclonal rat anti-macrophages/monocytes antibody (MOMA-2)-positive macrophages and α-smooth muscle actin (SMA)-positive smooth muscle cells mostly did not stain with the p16INK4a and p21 antibodies (Fig. 1c–f).

Figure 1
figure 1

Expression of p16INK4a/p21 was detected in CD31-positive ECs in the aortas of Ldlr−/− mice. Immunohistochemical staining of the ascending aorta in control-fed C57BL/6 and HFD-fed Ldlr−/− mice with anti-p16INK4a (a,c,e) and anti-p21 (b,d,f) antibodies. The aorta was coimmunostained with anti-CD31 (an ECs marker), MOMA-2 (a monocyte/macrophage marker), or anti-SMA (a marker for smooth muscle cells), and counterstained with Hoechst 33342 (blue). Dotted lines indicate the borders between blood vessel layers (intima and media). Scale bar: 50 μm.

The number of p16INK4a-positive cells in the aortic intima was markedly increased in the HFD/control water mice, whereas both drinking HW and oral administration (o.p.) of ABT-263 significantly suppressed this increase (Fig. 2a,b). Similarly, the number of p21-positive cells was markedly increased in the aortic intima in the HFD/control water group, and both HW and ABT-263 significantly suppressed this increase (Fig. 2a,c). To further examine whether cellular senescence was altered by HW, the mRNA levels of cellular senescence markers (p16INK4a, p21, p53) in the aortic arch were analyzed by quantitative reverse-transcription PCR (qPCR). Transcript levels of p16INK4a were significantly increased in all the HFD-fed groups compared with the groups that received a standard diet (Fig. 2d). Both drinking HW and ABT-263 o.p. significantly suppressed the increase in p16INK4a transcript levels. These results suggest that HW attenuates HFD-induced cellular senescence in the aorta, similarly to ABT-263.

Figure 2
figure 2

Drinking HW decreased HFD-induced p16INK4a and p21 expression in the ascending aorta in Ldlr−/− mice. (a) Immunohistochemical staining for p16INK4a and p21 (red) and Hoechst nuclear staining (blue) in the aortic intima. p16INK4a- and p21-positive cells were increased in HFD mice given control water (CW). These increases were suppressed in both HFD mice given HW and HFD mice treated with ABT-263 (ABT). Scale bar: 100 μm. (b) Quantitative analysis of p16-positive cells out of total cells. (c) Quantitative analysis of p21-positive cells out of total cells. (d) Transcript levels of cell senescence markers (p16INK4a, p21, and p53). Values are the mean ± SD (n = 6). *P < 0.05, **P < 0.01, and ***P < 0.001. ##P < 0.01 and ###P < 0.001 vs. C57BL/6 Ldlr+/+ control mice.

Drinking HW had little effect on lipid metabolism in HFD-fed Ldlr −/− mice

Atherosclerosis is induced by the accumulation of oxidized LDL in ECs. Oil Red O is a lysochrome (fat-soluble dye) diazo dye used for staining neutral triglycerides (TGs) and lipids, and conventionally used for measurement of the gross area of the atherosclerotic lesion18. The Oil Red O-positive area in the ascending aorta was markedly increased in all the HFD-fed groups, and drinking HW slightly suppressed this increase (Fig. 3a,b), indicating the possibility that lipid metabolism is affected by HW.

Figure 3
figure 3

Drinking HW had little effect on lipid metabolism in HFD-fed Ldlr−/− mice. (a) Oil Red O-positive areas in the vicinity of the aortic valve. The increase in the Oil Red O-positive area in HFD-fed mice given control water (CW) was not suppressed by either HW or ABT-263 (ABT). Scale bar: 500 μm. (b) Quantitative analysis of the Oil Red O-positive area in the ascending aorta. (c) TG, T-chol, HDL, and LDL levels in the plasma. (d) Representative images of fatty liver. Scale bar: 5 mm. (e) Quantitative analysis of the liver weight. Values are the mean ± SD (n = 6). *P < 0.05. ##P < 0.01 and ###P < 0.001 vs. C57BL/6 Ldlr+/+ control mice.

TG, total cholesterol (T-chol), high-density lipoprotein (HDL), and LDL levels in the blood plasma were markedly increased in all the HFD-fed groups (Fig. 3c). However, drinking HW did not prevent this increase in lipid levels. Similarly, hepatic steatosis was present in all the HFD-fed groups (Fig. 3d), and drinking HW neither improved the hepatic steatosis nor prevented the increase in liver weight (Fig. 3d,e). These results suggest that drinking HW has little or no effect on lipid metabolism in HFD-fed Ldlr−/− mice.

Drinking HW decreased macrophage infiltration into the aortic intima in HFD-fed Ldlr −/− mice

Foamy macrophages expressing senescence markers accumulate in the subendothelial space and drive atherosclerotic processes by increasing the expression of inflammatory cytokines and matrix metalloproteinases19,20. We therefore examined whether the numbers of infiltrating macrophages in the aortic intima were altered by drinking HW. The MOMA-2-positive area in the ascending aorta was markedly larger in the HFD/control water group (Fig. 4a,b). Both HW and ABT-263 significantly reduced the MOMA-2-positive area. To examine whether the expression of inflammatory cytokines and matrix metalloproteinases was altered by HW, their mRNA levels (Il1α, Tnfα, Mmp3, Mmp13, Mmp12) were measured by qPCR. Their transcript levels were markedly upregulated by HFD (Fig. 4c). Notably, both HW and ABT-263 significantly inhibited the upregulation of Tnfα. Recent studies indicate that CD36, a scavenger receptor of oxidized LDL in macrophage21, plays an important role in establishing the senescent phenotype22. We therefore examined the expression of CD36 in atherosclerotic regions and found that markedly increased level of CD36 in the HFD/control water group was significantly reduced by both HW and ABT-263 (Fig. 4d,e).

Figure 4
figure 4

Drinking HW decreased macrophage infiltration into the aortic intima in HFD-fed Ldlr−/− mice. (a) Immunohistochemical staining for MOMA-2 (red) and Hoechst nuclear staining (blue) in the aortic intima. MOMA-2-positive cells were increased in HFD mice given control water (CW). This increase was suppressed by both HW and ABT-263 (ABT). Scale bar: 100 μm. (b) Quantitative analysis of macrophage infiltration in the aortic intima. (c) Transcript levels of inflammatory cytokines (Il1α and Tnfα) and matrix metalloproteinases (Mmp3, Mmp13, and Mmp12). (d) Immunohistochemical staining for CD36 (green) and Hoechst nuclear staining (blue) in the aortic intima. CD36-positive cells were increased in HFD mice given control water (CW). This increase was suppressed by both HW and ABT-263 (ABT). Scale bar: 100 μm. (e) Quantitative analysis of CD36-positive cells in the aortic intima. Values are the mean ± SD (n = 6). *P < 0.05, **P < 0.01 and ***P < 0.001. #P < 0.05, ##P < 0.01 and ###P < 0.001 vs. C57BL/6 Ldlr+/+ control mice.

Suppression of cellular senescence by HW correlated with attenuation of macrophage infiltration

Immunohistochemical staining revealed that the increased MOMA-2-positive area in the HFD-fed groups shown in Fig. 4a,b significantly correlated with the numbers of p16INK4a- and p21-positive cells shown in Fig. 2a–c (Fig. 5a,d), supporting a strong association between macrophage activation and the development of senescence in the aorta. Both HW and ABT-263 suppressed the infiltration of macrophages and the accumulation of SCs in the aorta. On the other hand, the increased Oil Red O-positive area seen in HFD-fed mice shown in Fig. 3a,b did not correlate with the number of p16INK4a-positive or p21-positive cells (Fig. 5b,e), indicating that the effect of lipid accumulation on the induction of SCs was not stronger in the HFD-fed groups. Increased T-chol in the blood plasma also did not correlate with the number of p16INK4a- or p21-positive cells (Fig. 5c,f).

Figure 5
figure 5

HFD-induced macrophage infiltration correlated with p16INK4a/p21 expression. Scatter plots of the number of p16INK4a-positive (ac) and p21-positive (df) cells versus the MOMA-2-positive (a,d) and the Oil Red O-positive (b,e) area in the ascending aorta or versus the T-chol level in the plasma (c,f). Dots correspond to data from individual mice, as indicated. The Pearson’s correlation coefficient (r) and p-value (p) are shown.


The present study demonstrates that drinking HW improves vascular aging in the aorta. Many studies have shown that the cellular senescence markers p16INK4a and p21 are elevated in animal and human atherosclerotic plaques4,23,24,25. We showed that the HFD-induced increase in p16INK4a- and p21-positive ECs in the aortic intima (Fig. 1) was significantly suppressed by HW (Fig. 2). Drinking HW also significantly reduced the increase in p16INK4a transcript levels. Transcript levels of p21 were not significantly altered but tended to be suppressed by HW. However, p53 mRNA expression was not affected by any of the treatment conditions. Thus, p21 expression in this model might be regulated by signals other than p5326. Furthermore, neither HW nor ABT-263 decreased SA-β-Gal activity in the thoracic aorta in HFD-fed mice (Supplementary Fig. 1). Increase in SA-β-Gal activity is known to be an increase in lysosomal β-Gal activity and is not completely senescence-specific marker27,28. The discrepancy may be explained by the differential expression of CDK inhibitors (p16INK4a and p21) and SA-β-Gal. Childs et al. reported that foamy macrophages were highly positive for SA-β-Gal in HFD-fed Ldlr−/− mice11. However, previous studies showed that both p16INK4a- and p21-positive cells in atherosclerotic plaques are largely ECs and vascular smooth muscle cells4,23,24. Another possible explanation is cellular senescence at vascular branches and bends in Ldlr−/− mice29. We may have failed to observe the effects of drinking HW by focusing instead on the thoracic aorta, since the accumulation of SCs is lower there.

ROS can induce senescent growth arrest by triggering DNA damage response (DDR) pathways by transcriptional activation of p16INK4a and p2130. Activation of these CDK inhibitors generates ROS, which act as signaling molecules to promote the continuous induction of cellular senescence30. Remarkably, drinking HW ameliorates oxidative stress in animal disease models, including the Apoe−/− mouse model of atherosclerosis16, and in human clinical trials, including metabolic syndrome17,31 and rheumatoid arthritis32. One possible mechanistic explanation for the suppressive effect of HW on cellular senescence is that the lowering of ROS by HW downregulates DDR pathways. We demonstrated previously that H2 induces a nuclear factor erythroid 2-related factor 2 (Nrf2)-dependent antioxidant response in cultured cells33 and in a mouse model of sepsis16. A direct interaction between Nrf2 and p21 upregulates the antioxidant response34, which may downregulate further activation of DDR pathways. Interestingly, H2-rich medium alleviated dioxin-induced SA-β-Gal-positive cellular senescence in endothelial cells accompanying Nrf2 activation35. However, the atheroscrerotic lesions were markedly attenuated in the Nrf2 and Apoe double KO mice after 12 weeks on HFD and significantly amplified by the presence of Nrf2 in bone marrow-derived cells36. We then stained the aorta with anti-Nrf2 antibody and found that Nrf2 expression and its nuclear translocation tended to be enhanced by drinking HW in HFD-fed Ldlr−/− mice (Supplementary Fig. 2). Nrf2 usually works as an anti-inflammatory factor in various cell types including endotherial cells37. Further precise analysis in vitro and in vivo is needed to investigate whether HW-induced Nrf2 reduces expression of CDK inhibitors by lowering of ROS and inhibits Rb-mediated growth inhibition.

Hyperlipidemic conditions can accelerate atherosclerosis and vascular aging3,38. On the other hand, drinking HW ameliorated hyperlipidemia in HFD-fed hamsters39 and in patients with potential metabolic syndrome31. Administration of hydrogen-saturated saline decreased athero-susceptibility in apoB-containing lipoprotein and aortic atherosclerosis in Apoe−/− mice40. However, in the present study, HW and ABT-263 had little or no effect on lipid metabolism, with only a limited reduction in the area of the atheroma observed in HFD-fed Ldlr−/− mice (Fig. 3). On the other hand, HW significantly reduced an increase of CD36 expression in atherosclerotic region (Fig. 4). CD36 is one of the main scavenger receptors involved in the uptake of oxLDL by macrophages and has generally been viewed as essential for foam cell formation1. CD36 expression is known to be induced by oxLDL41, suggesting that HW-induced decrease of CD36 expression may depend on the slight suppression of lipid accumulation in the aorta by drinking HW. Another possibility is that H2 directly reduces CD36 expression in macrophages. We previously demonstrated that H2 inhibits fatty acid uptake and lipid accumulation through the downregulation of CD36 in human hepatoma HepG2 cells42.

A range of extrinsic and intrinsic stimuli including inflammatory responses, particularly those causing intracellular oxidative stress, can induce stress-induced premature senescence. In the previous study, atheroscrerotic lesions in Apoe KO mice were observed after 12 weeks on HFD diet3. Furthermore, elimination of foamy macrophages in Ldlr−/− mice prevented atherogenesis onset after 9 days on an atherogenic HFD diet11, indicating that atherogenesis after 13 weeks on HFD diet in our model is induced and enhanced by early and continuous inflammatory responses against hyperlipidemia and drinking HW may attenuate them. Indeed, drinking HW significantly suppressed macrophage infiltration and Tnfα transcription in the aortic arch of HFD-fed Ldlr−/− mice (Fig. 4). Tumor necrosis factor (TNF)-α is primarily produced by activated macrophages and can trigger premature senescence43. However, to clarify it, spatiotemporal analyses such as analyzing the atherosclerotic lesion using microdissection or in situ hybridization in different ages are necessary. In addition, immunohistochemical staining revealed that the increase in MOMA-2-positive macrophages significantly correlated with the numbers of both p16INK4a- and p21-ECs in the same aortic region (Fig. 5).

Several studies reported that H2 administration attenuated cellular inflammation and production of inflammatory cytokines in experimental animal models of inflammatory diseases such as zymosan-induced inflammation, inflammatory bowel disease, and lipopolysaccharide (LPS)-induced inflammation44,45,46. H2 inhibited LPS-induced phosphorylation of apoptosis signal-related kinase 1 (ASK1) via Toll-like receptors (TLRs)47. Signaling via TLRs activates macrophages, resulting in increased secretion of inflammatory cytokines48,49. Recent study showed the reduced expression of p16INK4a and p21 in the adipose tissue of TLR4-deficient aged mice50, indicating that drinking HW may attenuate cellular senescence by downregulation of TLR signaling. We then stained the aorta with anti-TLR4 antibody and found that drinking HW tended to suppress the increase TLR4 in atheroma, however it was not significant (Supplementary Fig. 3).

The body weight in the ABT-263 group gradually decreased during the course of this study (Supplementary Fig. 4). ABT-263, known as navitoclax, induces apoptosis through its inhibitory effect of the Bcl-2, Bcl-XL, and Bcl-W, and it acts at 5 nM in and has high specificity to senescent cells in cell experiments51. ABT-263 has been evaluated clinically in a number of trials, both as a monotherapy and in combination with chemotherapy in both solid tumors and hematologic malignancies, with dose-dependent thrombocytopenia as the major adverse effect52. On the other hand, any adverse effects of H2 administration have not been reported in animal and clinical studies53. Here, we showed that drinking HW suppresses cellular senescence in the aorta with no obvious adverse effects. Despite numerous studies reporting the antioxidant and anti-inflammatory effects of H2, the molecular mechanisms underlying its actions remain unclear. In the future, it will be important to clarify these mechanisms from the viewpoint of preventing senescence.

Materials and Methods


Female B6.129S7-Ldlrtm1Her/ J mice (Ldlr−/− mice) and female C57BL/6 J mice (specific pathogen-free) were purchased from Charles River Japan, Inc. (Tokyo, Japan). Mice were housed at 20–22 °C with a 12 h light/dark cycle and provided sterile food and water. All efforts were made to minimize the number of animals used and their suffering during experimental procedures. All protocols for animal use followed the Principles of Laboratory Animal Care (NIH publication no. 86-23, revised 1985). All study protocols were reviewed and approved by the Animal Care Committee of the Tokyo Metropolitan Institute of Gerontology.

HW administration

HW was prepared using a previously described method17. In brief, H2 gas (G1; Japan fine products, Kawasaki, Japan) was dissolved in reverse osmosis water under high pressure (0.4 MPa) to a super-saturated level in a stainless steel tank (Unicontrols, Chiba, Japan). Saturated HW was poured into aluminum foil bag equipped with an outlet line (Uchida Yoko, Tokyo, Japan) at atmosphere pressure. H2 concentration in water was monitored with Clark-type hydrogen microsensor (Unisense, Aarhus N, Denmark). H2 concentration in a tap HW ingested by mice at the end of outlet line was 400–700 μM. After drinking, H2 concentration in blood and organs was immediately increased and reached approximately 10 μM13,54, which was 100–1000 times higher than that of H2 (0.1–0.01 μM) produced by enterobacteria from their nutrients including lactulose15. Then, H2 was quickly exhaled as a gas15. During the preparation of HW, the H2 concentration in the air was carefully monitored using a H2 sensor with an alarm for safety, because H2 gas is explosive when the concentration in air is greater than 4%. Water obtained by degassing H2 from HW with gentle stirring overnight was used as a control. H2 concentration in a control water was no detectable (<1 nM), similarly to a tap water under the Earth’s standard atmosphere containing 0.5 ppm of H2. Mice were given water freely, and the vessel was freshly refilled with HW or control water every week. Every time before refill, we monitored H2 concentration in a tap HW used for a week and confirmed that it was approximately 400 μM or higher.

Experimental design

To induce atherosclerosis, Ldlr−/− mice were fed a HFD consisting of 36% calories from fat (H2HFD1; Oriental Yeast, Tokyo, Japan). To determine whether HW eliminates SCs, 10-week-old Ldlr−/− mice (n = 30) were randomly divided into five groups: 1) regular chow diet (control diet) with control water (n = 6); 2) control diet with HW (n = 6); 3) HFD with control water (n = 6); 4) HFD with HW (n = 6); and 5) HFD with control water and 50 mg/kg ABT-263 o.p. (Selleck Chemicals, Houston, TX, USA) in vehicle (corn oil with 10% dimethyl sulfoxide) once every 2 days during weeks 5–7 and 10–12 (n = 6). The dose of ABT-263 was referred to previous studies55. Female C57BL/6 J mice fed a control diet and provided control water in the same facility for the same term were used as an additional control.

After overnight fasting, mice were sacrificed at 13 weeks from the start of the experiment via exsanguination under deep anesthesia with combined anesthetic agents according to a previously described protocol16. In brief, three different anesthetic agents [0.75 mg/kg medetomidine hydrochloride (Domitol; Meiji Seika Pharma, Tokyo, Japan), 4 mg/kg midazolam (Dormicum; Astellas Pharma, Tokyo, Japan), and 5 mg/kg butorphanol (Vetorphale; Meiji Seika Pharma)] were mixed and administered to the mice by intraperitoneal injection. Plasma was isolated from heparinized blood by centrifugation at 2000 × g for 10 min at room temperature.

Analyses of plasma lipids

Plasma TG and T-chol levels were determined with enzymatic colorimetric methods according to the manufacturer’s protocol (Wako, Osaka, Japan). HDL and LDL levels were determined with enzymatic colorimetric methods according to the manufacturer’s protocol (Nittobo, Tokyo, Japan).

Oil Red O staining

Atheromatous plaques in the aorta were fixed in 4% paraformaldehyde, cryoprotected with sucrose, frozen, and cut into 8 μm sections. Sections were incubated with Oil Red O (Muto, Tokyo, Japan) for 15 min at 37 °C. After washing, sections were counterstained with hematoxylin (Wako) for 10 min at room temperature. The sections were scanned and observed on a whole slide scanner (Nanozoomer; Hamamatsu Photonics, Hamamatsu, Japan).


Aortas were fixed with 4% paraformaldehyde (Wako), cryoprotected with sucrose, frozen, and cut into 8 μm sections. Each section was blocked with goat serum and incubated overnight at 4 °C with primary antibodies against mouse antigens, as follows: monoclonal mouse anti-p16INK4a (1:200; Abcam, Cambridge, UK), monoclonal rabbit anti-p21(1:500; Abcam), monoclonal rat anti-CD31 (1:200; Abcam), MOMA-2 (1:25; Bio-Rad, Hercules, CA, USA), polyclonal goat anti-SMA (1:300; Abcam), monoclonal rabbit anti-CD36 (1:200; Abcam), monoclonal mouse anti-TLR4 (1:200; Abcam) and polyclonal rabbit anti-Nrf2 (1:200; C-20, Santa Cruz, Dallas, TX, USA). After washing, sections were further incubated with the appropriate secondary antibodies [Alexa Fluor 546-labeled goat anti-mouse IgG (1:500; ThermoFisher Scientific, Waltham, MA, USA), Alexa Fluor 546-labeled goat anti-rabbit IgG (1:500; ThermoFisher), Alexa Fluor 488-labeled goat anti-rat IgG (1:400; ThermoFisher), Alexa Fluor 594-labeled goat anti-rat IgG (1:400; ThermoFisher), Alexa Fluor 488-labeled donkey anti-goat IgG (1:500; ThermoFisher), Alexa Fluor 546-labeled donkey anti-mouse IgG (1:500; ThermoFisher), or Alexa Fluor 546-labeled donkey anti-rabbit IgG (1:500; ThermoFisher)] for 60 min at room temperature. The aortas were counterstained with Hoechst 33342 (1:2000; Nacalai, Tokyo, Japan) and imaged on a TCS SP8 laser confocal microscope (Leica, Wetzlar, Germany).

qPCR of senescence-associated genes

The fresh-frozen aortic arches were used for quantitative PCR analysis. Their total cellular RNA was extracted using the NucleoSpin kit (Macherey-Nagel, Düren, Germany) and subjected to reverse transcription using a first-strand synthesis system (SuperScript II; ThermoFisher Scientific) according to the manufacturer’s protocol. qPCR was performed using SYBR Green (Toyobo, Osaka, Japan) according to the manufacturer’s recommendations, and target gene expression was normalized to the expression of Rpl4 in each sample. The primers used for amplification of p16INK4a, p19Arf, p21, p53, Il1α, Tnfα, Mmp3, Mmp13, Mmp12, and Rpl4 cDNAs are listed in Table 1.

Table 1 Primers used for semiquantitative PCR.

Statistical analysis

Statistical analyses were performed using SPSS software (version 22.0; SPSS, Chicago, IL, USA). All values are presented as the means ± standard deviation (SEM). Significance was obtained by one-way ANOVA with Tukey’s test. The Pearson’s correlation coefficient was used to test correlations. Results were considered significant at P < 0.05.