- Open Access
Hyperhomocysteinemia induced by excessive methionine intake promotes rupture of cerebral aneurysms in ovariectomized rats
© The Author(s). 2016
Received: 10 December 2015
Accepted: 21 June 2016
Published: 27 June 2016
Hyperhomocysteinemia (HHcy) is associated with inflammation and a rise in the expression of matrix metalloproteinase-9 (MMP-9) in the vascular wall. However, the role of HHcy in the growth and rupture of cerebral aneurysms remains unclear.
Thirteen-week-old female Sprague-Dawley rats were subject to bilateral ovariectomy and ligation of the right common carotid artery and fed an 8 % high-salt diet to induce cerebral aneurysms. Two weeks later, they underwent ligation of the bilateral posterior renal arteries. They were divided into two groups and methionine (MET) was or was not added to their drinking water. In another set of experiments, the role of folic acid (FA) against cerebral aneurysms was assessed.
During a 12-week observation period, subarachnoid hemorrhage due to aneurysm rupture was observed at the anterior communicating artery (AcomA) or the posterior half of the circle of Willis. HHcy induced by excessive MET intake significantly increased the incidence of ruptured aneurysms at 6–8 weeks. At the AcomA of rats treated with MET, we observed the promotion of aneurysmal growth and infiltration by M1 macrophages. Furthermore, the mRNA level of MMP-9, the ratio of MMP-9 to the tissue inhibitor of metalloproteinase-2, and the level of interleukin-6 were higher in these rats. Treatment with FA abolished the effect of MET, suggesting that the inflammatory response and vascular degradation at the AcomA is attributable to HHcy due to excessive MET intake.
We first demonstrate that in hypertensive ovariectomized rats, HHcy induced by excessive MET intake may be associated with the propensity of the aneurysm wall to rupture.
Subarachnoid hemorrhage (SAH) due to the rupture of cerebral aneurysms is a catastrophic event; its mortality rate is high despite advances in surgical techniques and perioperative management. Surgical clipping or endovascular coiling can be performed to prevent aneurysmal rupture. However, the mortality and morbidity rate after the clipping or coiling of unruptured aneurysms is not negligible . A better understanding of the pathogenesis underlying the growth and rupture of cerebral aneurysms is needed to establish new therapeutic strategies.
Homocysteine (Hcy) is a non-protein-forming, sulphur-containing, non-essential amino acid that functions as a key intermediate in the methionine (MET) metabolism . Hcy connects the MET- with the folate cycle. Several B vitamins play a role in the Hcy metabolism and an imbalance in the formation and removal of Hcy elicits changes in the plasma Hcy level. Some clinical studies suggested hyperhomocysteinemia (HHcy) as a strong independent factor in coronary disease, stroke, and abdominal aortic aneurysms [3–5]. Halazun et al.  reported that inflammation and matrix metalloproteinase (MMP)-2 and MMP-9 induced by HHcy are key factors in the growth of abdominal aortic aneurysms. Xu et al.  reported that in rats, HHcy induced by a MET-containing diet accelerated the formation of cerebral aneurysms, and Semmler et al.  suggested that polymorphisms affecting the Hcy metabolism were associated with the formation of cerebral aneurysms. However, the role of HHcy in the cerebral vascular structure and in the growth and rupture of cerebral aneurysms remains poorly understood.
Based on epidemiologic evidence of a high incidence of cerebral aneurysms in postmenopausal women, we established a cerebral aneurysm model in female rats subjected to hemodynamic stress, estrogen deficiency, and hypertension [9, 10]. We demonstrated that estrogen deficiency was associated with endothelial damage and that hypertension promoted the progression of cerebral aneurysms . Activation of the local renin-angiotensin system (RAS), oxidative stress, inflammation, and sodium retention were associated with the formation of cerebral aneurysms [12–14]. Despite the high incidence of aneurysm formation at the anterior cerebral artery-olfactory artery (ACA-OA) bifurcation of rats, none of these aneurysms ruptured [9–15]. However, some aneurysms developed not only at the anterior communicating artery (AcomA) but also at the posterior half of the circle of Willis (PW), and they ruptured . The PW includes the posterior communicating and the posterior cerebral artery (PcomA, PCA).
In humans, the hazard ratio of rupture was significantly higher for aneurysms at the AcomA and the PcomA than for middle cerebral artery (MCA) aneurysms . A better understanding of the mechanisms underlying their growth and rupture is of clinical importance. We examined the role of HHcy in the growth and rupture of cerebral aneurysms at the AcomA and PW.
Here, we show that HHcy induced by excessive MET intake promoted the rupture of rat cerebral aneurysms at the AcomA and PW and the growth of aneurysms at the AcomA and that these events were associated with an increase in pro-inflammatory-and vascular degradation molecules.
All procedures were performed with the rats under 2–4 % isoflurane inhalation anesthesia.
For aneurysm induction, 13-week-old female Sprague-Dawley rats were subjected to right common carotid artery (CCA) ligation to induce hemodynamic stress at the left ACA-OA bifurcation and the AcomA. They also underwent bilateral ovariectomy immediately after right CCA ligation. Starting on the next day, they were fed a high-salt diet (8 % sodium chloride). Two weeks later, they were subjected to ligation of the bilateral posterior renal arteries to induce hypertension. The time point of aneurysm induction was defined as the time of bilateral posterior renal artery ligation.
Experiment 1: To assess the incidence of SAH and the morphological aneurysmal wall changes, we prepared two groups. One group (MET, n = 25) did, and the other (control, n = 19) did not receive 4 mg/ml MET (Wako, Osaka, Japan) in their drinking water. At 12 weeks after aneurysm induction, we prepared vascular corrosion casts of all asymptomatic rats. In a separate experiment, another set of rats (MET, n = 6; control, n = 6) was used to analyze the mRNA level by quantitative real-time polymerase chain reaction (qRT-PCR) assay and the results were compared with sham-operated rats (sham, n = 6) fed with a standard diet including 0.3 % sodium chloride.
Experiment 2: To test whether folic acid (FA) prevents the growth and rupture of cerebral aneurysms, another set of 19 MET rats was fed FA (Sigma-Aldrich, Tokyo, Japan) daily (4 mg/kg; MET + FA rats) to attenuate the conversion from MET to Hcy. They were compared with 35 MET-only rats. The administration of FA and MET was started at the same time. We also prepared six additional rats in each group for qRT-PCR assay. The MET and FA doses were based on findings reported in earlier studies [7, 17, 18].
Rats that died within 4 weeks after aneurysm induction were excluded. As 2 to 8 weeks are needed for plasma Hcy to return to the normal level in rats given a diet containing FA , we began evaluating its effects on aneurysmal rupture 4 weeks after the start of FA administration. The observation period was 12 weeks. To detect aneurysmal rupture, two blinded observers performed daily neurological examinations and recorded neurological signs, i.e., motor deficits, seizures, absence of spontaneous activity, and death. The brains of all symptomatic rats harbored cerebral aneurysms and manifested SAH. None of the asymptomatic rats that survived for 12 weeks suffered SAH. We defined the incidence of ruptured aneurysms as the ratio of rats with ruptured aneurysms to the total number of rats. Ruptured aneurysms were observed under a stereomicroscope after removing the SAH thrombus.
Blood pressure and plasma Hcy measurements
For blood pressure readings, once every 4 weeks, unanesthetized rats were placed on a 37 °C hot plate (NISSIN, Tokyo, Japan) and covered with a black blanket. After acclimatization, one blinded examiner recorded their average blood pressure based on three measurements obtained with the tail-cuff method (Softron, Tokyo, Japan). Blood was withdrawn 12 weeks after the last procedure; plasma samples were stored at −80 °C until use. In humans, plasma Hcy levels exceeding 15 nmol are recorded as HHcy .
Preparation of vascular corrosion casts
Vascular corrosion casts were prepared as previously described . Rats were transcardially perfused with heparinized phosphate-buffered saline (PBS) followed by the injection of Batson’s No. 17 plastic (Polyscience Inc., Warrington, PA, USA). The left ACA-OA bifurcation and the AcomA on the casts were inspected at 3 kV under a scanning electron microscope (VE8800, Keyence, Osaka, Japan). Morphological changes at the AcomA were evaluated by three blinded observers and classified into four stages where stage 0 = no arterial dilation or irregular shapes, stage 1 = slight protrusion (diameter of the aneurysmal protrusion < half of the diameter of the parent artery), stage 2 = moderate protrusion (half the diameter of the parent artery < diameter of the protrusion < diameter of the parent artery), and stage 3 = a well-developed saccular aneurysm (diameter of the aneurysm > diameter of the parent artery).
RNA isolation and qRT-PCR assay
For rat MMP-9: forward primer (F), 5′-ACA ACG TCT TTC ACT ACC AA-3′, reverse primer (R), 5′-CAA AAG AGG AGC CTT AGT TC-3′
for TIMP1: F, 5′-TCC TGG TTC CCT GGC ATA AT-3′, R, 5′-GGC AAA GTG ATC GCT CTG GT-3′
for TIMP2: F, 5′-CCC TCT GTG ACT TTA TTG TGC-3′, R, 5′-TGA TGC TCT TCT CTG TGA CC-3′
for NOX4: F, 5′-AGA CAT CCA ATC ATT CCA GTG GTT TGC AGA C-3′, R, 5′-TGC TCT ATG TGC TGC ATA ACA AGT TTT GGC AA-3′
for Rac1: F, 5′-CTG TCT TGA GTC CTC GCT GTG TGA GTG CTG-3′, R, 5′-CAG CAG GCA TTT TCT CTT CC-3′
for TNFα, F, 5′-CCC AAC AAG GAG GAG AAG T-3′, R, 5′-CGC TTG GTG GTT TGC TAC-3′
for IL-6, F, 5′-TCT CAG GGA GAT CTT GGA AAT G-3′, R, 5′-TAG AAA CGG AAC TCC AGA AGA C-3′
for GAPDH, F, 5′-TAC ACT GAG GAC CAG GTT G-3′, R, 5′-CCC TGT TGC TGT AGC CAT A-3′.
Primers and probe sets for ACE were from Roche and used according to the manufacturer’s directions. The amplified product was separated on 1.5 % agarose gels containing EtBr solution (Wako, Osaka, Japan) and visualized on an ultraviolet transilluminator. The results were quantified after normalization to the expression of GAPDH mRNA. The PCR conditions were 95 °C for 10 min followed by 40 cycles at 95 °C for 10 s, 60 °C for 10 s, and 72 °C for 8 s. We subjected samples from each group to two independent qRT-PCR assays. GAPDH was the internal control.
In a separate set of experiments, 3 MET and 3 control rats were prepared for immunofluorescence studies. After perfusion with 4 % paraformaldehyde, we inspected the vessels in the circle of Willis under a dissecting microscope. The AcomA was carefully dissected and immersed in 4 % paraformaldehyde. The arteries were rinsed with PBS, embedded in OCT compound (Tissue-Tek, Inc.), and 6-μm-thick serial sections were cut with a cryotome (CM 1850; Leica). After 30-min serum-free protein blockade (Dako, Carpinteria, CA, USA), primary antibodies diluted with Canget signal immunostain (Toyobo, Osaka, Japan) were added for 1-h incubation at room temperature (RT) or overnight at 4 °C. Primary antibodies against MMP-9, CD163 (Abcam, CA, USA), CD11b (BioLegend, CA, USA), and CD68 (Abbiotec, CA, USA) were applied. Sections were then incubated for 1 h at RT with the fluorescein-conjugated secondary antibodies Alexa Fluor 488 or 594 (Molecular Probes, CA, USA) in Canget signal immunostain, mounted with Vectashield (Vector Laboratories, CA, USA), and examined under a fluorescence microscope (Olympus IX71, Tokyo, Japan).
Sequentially obtained data (mean ± SD) were analyzed with Student’s t test for 2-group comparisons and analysis of variance (ANOVA) followed by Scheffe’s test for multiple comparisons. The incidence of ruptured aneurysms and of cerebral aneurysmal changes was analyzed with Fisher’s exact probability test. Statistical analyses were performed with statistical software (StatView 5). Differences were considered statistically significant at p < 0.05.
Excessive MET intake promotes the rupture of rat cerebral aneurysms
Excessive MET intake may increase the vulnerability of the AcomA wall
Excessive MET intake is associated with increased M1 macrophage infiltration into the AcomA wall and with vascular degradation
The inhibition of conversion from MET to Hcy attenuates the development of AcomA aneurysms by inhibiting vascular degradation
In this study, we first demonstrate that HHcy induced by excessive MET intake promotes the growth of AcomA-and the rupture of AcomA and PW aneurysms. In MET rats, we observed an increase in the infiltration of M1 macrophages, the expression of MMP-9, and the ratio of MMP-9 to TIMP2 at the AcomA. Treatment with FA reduced HHcy, attenuated the effects of MET, and prevented the growth and rupture of aneurysms. Our findings suggest that the vulnerability of the AcomA wall in MET rats is at least partly attributable to HHcy and that its suppression may help to prevent the growth and/or rupture of cerebral aneurysms.
Up to 40 % of patients diagnosed with premature coronary artery disease, peripheral vascular disease, or recurrent venous thrombosis manifested HHcy [21, 22]. However, it is unclear whether HHcy is a causative factor or a result of these diseases. In mice, the oral administration of FA or of a combination of B vitamins decreased HHcy and attenuated atherogenesis . These observations support our present findings that HHcy promotes the growth and rupture of cerebral aneurysms.
In humans, efforts to lower HHcy by therapy with FA and vitamin B did not reduce the incidence of cardiovascular events [22, 24]. The daily combined intake of FA and vitamins B6 and B12 for 5 years failed to significantly reduce the rate of major vascular events in a high-risk population with vascular disease, possibly because it failed to reverse epigenetic changes induced by HHcy . Saposnik et al.  found that while FA helped to lower Hcy and vitamins B6 and B12 reduced the overall risk for stroke, there was no effect on stroke severity and post-stroke disability. On the other hand, among adult hypertensive Chinese with no history of stroke or myocardial infarction, the combined use of enalapril, an angiotensin-converting enzyme inhibitor, and FA significantly reduced the risk for a first stroke, compared to patients treated with enalapril alone . Epigenetic factors may contribute differently to cardiovascular and cerebrovascular diseases. Combination therapies aimed at improving the epigenetic machinery and lowering circulating Hcy levels may be more beneficial. Since the blood pressure in our MET + FA rats was not affected, we posit that HHcy contributed to the growth and rupture of their cerebral aneurysms in a blood pressure-independent manner.
Many macrophages were observed in the human luminal and abluminal layer of large unruptured and ruptured aneurysms [27, 28]. Elsewhere, we demonstrated that in our rat aneurysm model, the degradation of endothelial tight junctions facilitated macrophage infiltration into the vascular wall . While pro-inflammatory M1 and anti-inflammatory M2 macrophages were present in equal proportion in unruptured aneurysms, the number of M1 macrophages was increased in ruptured aneurysms . Yao et al. reported that IL-6 increased MMP-9 activity in human cerebral smooth muscle cells in vitro . Tissue-infiltrating macrophages not only release pro-inflammatory cytokines that lead to the recruitment of additional inflammatory cells, but they also release MMPs that digest the extracellular matrix of the arterial wall, resulting in further damage via the up-regulation of other proteinases. Thus, the infiltration of macrophages and macrophage-derived MMPs may be closely associated with aneurysmal growth. The increase in CD68+/CD11b+ macrophages and the elevated mRNA level of IL-6 in the AcomA wall of MET rats may reflect this phenomenon.
On the other hand, others [32, 33] reported that the highest wall shear stress involved the AcomA rather than other cerebral arterial bifurcations and that it was highly oscillatory. Oscillatory wall shear stress increased the expression of MMP-9 in endothelial cells  and Sho et al.  reported that high flow and shear stress can induce endothelial and smooth muscle cells to express MMP-2 and MMP-9; they also documented a disproportional increase in TIMP2. As we did not directly assess the blood flow, we cannot comment on the relationship between hemodynamics and the propensity of AcomA aneurysms to rupture. Whether the imbalance between MMP-9 and TIMP2 at the AcomA is associated with complex hemodynamics remains to be determined. The expression of macrophage-derived MMP-9 is critical for vascular wall remodeling. It was significantly increased in the wall of cerebral aneurysms in rats exposed to HHcy  and the selective inhibition of MMP blocked aneurysmal progression . Therapies targeting MMP-9 and TIMP2 may be promising candidates in efforts to prevent the growth and rupture of cerebral aneurysms.
Elsewhere [11–15], we reported that RAS, oxidative stress, and inflammation were strongly associated with the formation of cerebral aneurysms. In the current study, the expression of these molecules was higher in both our MET and control rats than in the sham rats. However, there was no significant difference between MET and control rats although the MET rats harbored a significantly higher grade of AcomA aneurysms than the controls, suggesting that these molecules may be associated with the formation of cerebral aneurysms but that they may not be directly associated with aneurysmal growth or rupture.
Our study has some limitations. As it was difficult to obtain samples just after rupture, we could not assess differences in the molecule levels between ruptured and unruptured AcomA aneurysms. We also did not determine whether the AcomA used for the analysis of the mRNA level harbored aneurysms. Although we document the relationship between the increase in degradation molecules and AcomA aneurysms with an unstable wall, we were unable to identify the detailed mechanisms underlying aneurysmal rupture. Since we excluded rats with ruptured aneurysms at the PW, there is sampling bias in assessment of aneurysmal changes at AcomA (Figs. 2b and 6b).
We provide new evidence that HHcy elicited by an excessive MET intake is associated with the vulnerability of the vascular wall at the AcomA. Suppressing inflammation, vascular degradation, and macrophage infiltration may prevent aneurysmal rupture. Our findings may pave the way for the development of pharmacological therapies to address human cerebral aneurysms.
ACA-OA, anterior cerebral artery-olfactory artery; ACE, angiotensin-converting enzyme; AcomA, anterior communicating artery; CCA, common carotid artery; FA, folic acid; Hcy, homocysteine; HHcy, hyperhomocysteinemia; IL, interleukin; MMP, matrix metalloproteinase; PW, posterior half of the circle of Willis; qRT-PCR, quantitative real-time polymerase chain reaction; RAS, renin-angiotensin system; SAH, subarachnoid hemorrhage; TIMP, tissue inhibitor of metalloproteinase; TNF, tumor necrosis factor
We thank Dr. Yoshiro Kanasaki of the Faculty of Medicine, Tokushima University Graduate School, for technical assistance.
This work was supported by a Grant-in-Aid for Scientific Research from the Ministry of Education, Science, Sports, and Culture of Japan, by the Strategic Young Researcher Overseas Visits Program for Accelerating Brain Circulation from the Japan Society for the Promotion of Science, and by Kanae Foundation for the Promotion of Medical Science.
Availability of data and materials
Data supporting the conclusions of this article are included within the manuscript.
MK, KTK, and YT participated in the study design. MK and TM performed all experimental studies and data analyses. YT, KS, and NM evaluated the imaging data. MK wrote the paper. YK, JS, TH, and SN supervised the study. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
Ethics approval and consent to participate
All experiments and protocols were approved by the ethics committee of Tokushima University. They were conducted in accordance with the National Institutes of Health Guide for the Care and Use of Laboratory Animals.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
- Wiebers DO, Whisnant JP, Huston 3rd J, Meissner I, Brown Jr RD, Piepgras DG, et al. Unruptured intracranial aneurysms: natural history, clinical outcome, and risks of surgical and endovascular treatment. Lancet. 2003;362(9378):103–10.View ArticlePubMedGoogle Scholar
- Refsum H, Smith AD, Ueland PM, Nexo E, Clarke R, McPartlin J, et al. Facts and recommendations about total homocysteine determinations: an expert opinion. Clin Chem. 2004;50(1):3–32.View ArticlePubMedGoogle Scholar
- Boushey CJ, Beresford SA, Omenn GS, Motulsky AG. A quantitative assessment of plasma homocysteine as a risk factor for vascular disease. Probable benefits of increasing folic acid intakes. JAMA. 1995;274(13):1049–57.View ArticlePubMedGoogle Scholar
- Nygard O, Nordrehaug JE, Refsum H, Ueland PM, Farstad M, Vollset SE. Plasma homocysteine levels and mortality in patients with coronary artery disease. N Engl J Med. 1997;337(4):230–6.View ArticlePubMedGoogle Scholar
- Brunelli T, Prisco D, Fedi S, Rogolino A, Farsi A, Marcucci R, et al. High prevalence of mild hyperhomocysteinemia in patients with abdominal aortic aneurysm. J Vasc Surg. 2000;32(3):531–6.View ArticlePubMedGoogle Scholar
- Halazun KJ, Bofkin KA, Asthana S, Evans C, Henderson M, Spark JI. Hyperhomocysteinaemia is associated with the rate of abdominal aortic aneurysm expansion. Eur J Vasc Endovasc Surg. 2007;33(4):391–4. discussion 5-6.View ArticlePubMedGoogle Scholar
- Xu Y, Tian Y, Wei HJ, Dong JF, Zhang JN. Methionine diet-induced hyperhomocysteinemia accelerates cerebral aneurysm formation in rats. Neurosci Lett. 2011;494(2):139–44.View ArticlePubMedGoogle Scholar
- Semmler A, Linnebank M, Krex D, Gotz A, Moskau S, Ziegler A, et al. Polymorphisms of homocysteine metabolism are associated with intracranial aneurysms. Cerebrovasc Dis. 2008;26(4):425–9.View ArticlePubMedGoogle Scholar
- Jamous MA, Nagahiro S, Kitazato KT, Satomi J, Satoh K. Role of estrogen deficiency in the formation and progression of cerebral aneurysms. Part I: experimental study of the effect of oophorectomy in rats. J Neurosurg. 2005;103(6):1046–51.View ArticlePubMedGoogle Scholar
- Jamous MA, Nagahiro S, Kitazato KT, Tamura T, Kuwayama K, Satoh K. Role of estrogen deficiency in the formation and progression of cerebral aneurysms. Part II: experimental study of the effects of hormone replacement therapy in rats. J Neurosurg. 2005;103(6):1052–7.View ArticlePubMedGoogle Scholar
- Tamura T, Jamous MA, Kitazato KT, Yagi K, Tada Y, Uno M, et al. Endothelial damage due to impaired nitric oxide bioavailability triggers cerebral aneurysm formation in female rats. J Hypertens. 2009;27(6):1284–92.View ArticlePubMedGoogle Scholar
- Tada Y, Kitazato KT, Tamura T, Yagi K, Shimada K, Kinouchi T, et al. Role of mineralocorticoid receptor on experimental cerebral aneurysms in rats. Hypertension. 2009;54(3):552–7.View ArticlePubMedGoogle Scholar
- Yagi K, Tada Y, Kitazato KT, Tamura T, Satomi J, Nagahiro S. Ibudilast inhibits cerebral aneurysms by down-regulating inflammation-related molecules in the vascular wall of rats. Neurosurgery. 2010;66(3):551–9. discussion 9.View ArticlePubMedGoogle Scholar
- Matsushita N, Kitazato KT, Tada Y, Sumiyoshi M, Shimada K, Yagi K, et al. Increase in body Na+/water ratio is associated with cerebral aneurysm formation in oophorectomized rats. Hypertension. 2012;60(5):1309–15.View ArticlePubMedGoogle Scholar
- Tada Y, Kitazato KT, Yagi K, Shimada K, Matsushita N, Kinouchi T, et al. Statins promote the growth of experimentally induced cerebral aneurysms in estrogen-deficient rats. Stroke. 2011;42(8):2286–93.View ArticlePubMedGoogle Scholar
- Morita A, Kirino T, Hashi K, Aoki N, Fukuhara S, et al. The natural course of unruptured cerebral aneurysms in a Japanese cohort. N Engl J Med. 2012;366(26):2474–82.View ArticlePubMedGoogle Scholar
- Dai J, Li W, Chang L, Zhang Z, Tang C, Wang N, et al. Role of redox factor-1 in hyperhomocysteinemia-accelerated atherosclerosis. Free Radic Biol Med. 2006;41(10):1566–77.View ArticlePubMedGoogle Scholar
- Lee H, Kim JM, Kim HJ, Lee I, Chang N. Folic acid supplementation can reduce the endothelial damage in rat brain microvasculature due to hyperhomocysteinemia. J Nutr. 2005;135(3):544–8.PubMedGoogle Scholar
- Austin RC, Lentz SR, Werstuck GH. Role of hyperhomocysteinemia in endothelial dysfunction and atherothrombotic disease. Cell Death Differ. 2004;11 Suppl 1:S56–64.View ArticlePubMedGoogle Scholar
- Jamous MA, Nagahiro S, Kitazato KT, Satoh K, Satomi J. Vascular corrosion casts mirroring early morphological changes that lead to the formation of saccular cerebral aneurysm: an experimental study in rats. J Neurosurg. 2005;102(3):532–5.View ArticlePubMedGoogle Scholar
- den Heijer M, Koster T, Blom HJ, Bos GM, Briet E, Reitsma PH, et al. Hyperhomocysteinemia as a risk factor for deep-vein thrombosis. N Engl J Med. 1996;334(12):759–62.View ArticleGoogle Scholar
- Krishna SM, Dear A, Craig JM, Norman PE, Golledge J. The potential role of homocysteine mediated DNA methylation and associated epigenetic changes in abdominal aortic aneurysm formation. Atherosclerosis. 2013;228(2):295–305.View ArticlePubMedGoogle Scholar
- Hofmann MA, Lalla E, Lu Y, Gleason MR, Wolf BM, Tanji N, et al. Hyperhomocysteinemia enhances vascular inflammation and accelerates atherosclerosis in a murine model. J Clin Invest. 2001;107(6):675–83.View ArticlePubMedPubMed CentralGoogle Scholar
- Lonn E, Yusuf S, Arnold MJ, Sheridan P, Pogue J, Micks M, et al. Homocysteine lowering with folic acid and B vitamins in vascular disease. N Engl J Med. 2006;354(15):1567–77.View ArticlePubMedGoogle Scholar
- Saposnik G, Ray JG, Sheridan P, McQueen M, Lonn E. Heart outcomes prevention evaluation I. Homocysteine-lowering therapy and stroke risk, severity, and disability: additional findings from the HOPE 2 trial. Stroke. 2009;40(4):1365–72.View ArticlePubMedGoogle Scholar
- Huo Y, Li J, Qin X, Huang Y, Wang X, Gottesman RF, et al. Efficacy of folic acid therapy in primary prevention of stroke among adults with hypertension in China: the CSPPT randomized clinical trial. JAMA. 2015;313(13):1325–35.View ArticlePubMedGoogle Scholar
- Nakajima N, Nagahiro S, Sano T, Satomi J, Tada Y, Yagi K, et al. Kruppel-like zinc-finger transcription factor 5 (KLF5) is highly expressed in large and giant unruptured cerebral aneurysms. World Neurosurg. 2012;78(1-2):114–21.View ArticlePubMedGoogle Scholar
- Chalouhi N, Hoh BL, Hasan D. Review of cerebral aneurysm formation, growth, and rupture. Stroke. 2013;44(12):3613–22.View ArticlePubMedGoogle Scholar
- Tada Y, Yagi K, Kitazato KT, Tamura T, Kinouchi T, Shimada K, et al. Reduction of endothelial tight junction proteins is related to cerebral aneurysm formation in rats. J Hypertens. 2010;28(9):1883–91.View ArticlePubMedGoogle Scholar
- Hasan D, Chalouhi N, Jabbour P, Hashimoto T. Macrophage imbalance (M1 vs. M2) and upregulation of mast cells in wall of ruptured human cerebral aneurysms: preliminary results. J Neuroinflamm. 2012;9:222.View ArticleGoogle Scholar
- Yao JS, Zhai W, Fan Y, Lawton MT, Barbaro NM, Young WL, et al. Interleukin-6 upregulates expression of KDR and stimulates proliferation of human cerebrovascular smooth muscle cells. J Cereb Blood Flow Metab. 2007;27(3):510–20.View ArticlePubMedGoogle Scholar
- Alfano JM, Kolega J, Natarajan SK, Xiang J, Paluch RA, Levy EI, et al. Intracranial aneurysms occur more frequently at bifurcation sites that typically experience higher hemodynamic stresses. Neurosurgery. 2013;73(3):497–505.View ArticlePubMedGoogle Scholar
- Nam SW, Choi S, Cheong Y, Kim YH, Park HK. Evaluation of aneurysm-associated wall shear stress related to morphological variations of circle of Willis using a microfluidic device. J Biomech. 2015;48(2):348–53.View ArticlePubMedGoogle Scholar
- Magid R, Murphy TJ, Galis ZS. Expression of matrix metalloproteinase-9 in endothelial cells is differentially regulated by shear stress. Role of c-Myc. J Biol Chem. 2003;278(35):32994–9.View ArticlePubMedGoogle Scholar
- Sho E, Sho M, Singh TM, Nanjo H, Komatsu M, Xu C, et al. Arterial enlargement in response to high flow requires early expression of matrix metalloproteinases to degrade extracellular matrix. Exp Mol Pathol. 2002;73(2):142–53.View ArticlePubMedGoogle Scholar
- Aoki T, Kataoka H, Morimoto M, Nozaki K, Hashimoto N. Macrophage-derived matrix metalloproteinase-2 and -9 promote the progression of cerebral aneurysms in rats. Stroke. 2007;38(1):162–9.View ArticlePubMedGoogle Scholar