Relationship between peroxisome proliferator-activated receptor-γ mRNA expression and intracranial aneurysm rupture

被引:0
|
作者
Zhang, Xiong [1 ]
Kang, Yan-Xun [2 ]
Kong, Wei [3 ]
Zhang, Ya-Lan [1 ]
Ju, Tao [4 ]
机构
[1] First Peoples Hosp Xianyang, Dept Lab, Xianyang, Shaanxi, Peoples R China
[2] First Peoples Hosp Xianyang, Dept Med Imaging, Xianyang, Shaanxi, Peoples R China
[3] First Peoples Hosp Xianyang, Dept Neurol, Xianyang, Shaanxi, Peoples R China
[4] Yanan Univ, Dept Neurosurg, Xianyang Hosp, Xianyang, Shaanxi, Peoples R China
关键词
inflammation; interleukin-6; intracranial aneurysm; intracranial aneurysm rupture; peroxisome proliferator-activated receptor-gamma; subarachnoid hemorrhage; RISK; HEMORRHAGE; PPAR; MICE;
D O I
10.1177/20587392211028720
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
It has been reported that the normal adults can suffer from an intracranial aneurysm (IA) that might present the risk of rupture and cause the subarachnoid hemorrhage. Peroxisome proliferator-activated receptor-gamma (PPAR-gamma) as a nuclear hormone receptor has been identified to involve in the progress of the formation and rupture of IAs. Quantitative reverse transcription polymerase chain reaction (qRT-PCR) was used to detect PPAR-gamma mRNA expression in the macrophages of the patients with IAs. The information including fasting blood glucose (FBG), interleukin-6 (IL-6), and systolic blood pressure (SBP) were collected. The aneurysm parameters of all the participants were obtained through the cerebral angiography. Establishing the receiver-operating characteristic curve (ROC curve) evaluated the clinical significances of PPAR-gamma mRNA for IAs rupture. In this study, we observed that the rupture of IAs was caused by the maximum height of aneurysm > 7 mm, the location of aneurysm in posterior communicating artery (PCOM) or anterior communicating artery (ACOM), and the increase of aneurysm size ratio (SR). The levels of SBP and IL-6 in the rupture group were higher than those in the unrupture group, and PPAR-gamma mRNA expression in the rupture group was also significantly reduced. In addition, heavy drinking was statistically significant between the ruptured and unruptured groups. There was no significant difference in serum FBG level between the two groups. The evidences of this study showed that PPAR-gamma mRNA was negatively correlated with SBP, SR, and IL-6 levels in rupture group, respectively. The AUC of PPAR-gamma mRNA in ROC curve was 0.867, indicating that the change of PPAR-gamma mRNA level had obvious effect on IAs rupture. The aim of this study was to evaluate the potential of PPAR-gamma in macrophages to prevent IAs rupture.
引用
收藏
页数:10
相关论文
共 50 条
  • [21] Catalposide is a natural agonistic ligand of peroxisome proliferator-activated receptor-α
    Lee, Ji Hae
    Jun, Hee-jin
    Hoang, Minh-Hien
    Jia, Yaoyao
    Han, Xiang Hua
    Lee, Dong-Ho
    Lee, Hak-Ju
    Hwang, Bang Yeon
    Lee, Sung-Joon
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2012, 422 (04) : 568 - 572
  • [22] Protective Role of Peroxisome Proliferator-activated Receptor-β/δ in Septic Shock
    Kapoor, Amar
    Shintani, Yasunori
    Collino, Massimo
    Osuchowski, Marcin F.
    Busch, Daniel
    Patel, Nimesh S. A.
    Sepodes, Bruno
    Castiglia, Sara
    Fantozzi, Roberto
    Bishop-Bailey, David
    Mota-Filipe, Helder
    Yaqoob, Muhammad M.
    Suzuki, Ken
    Bahrami, Soheyl
    Desvergne, Beatrice
    Mitchell, Jane A.
    Thiemermann, Christoph
    AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2010, 182 (12) : 1506 - 1515
  • [23] Inhibition of corneal neovascularization by a peroxisome proliferator-activated receptor-γ ligand
    Sarayba, MA
    Li, L
    Tungsiripat, T
    Liu, NH
    Sweet, PM
    Patel, AJ
    Osann, KE
    Chittiboyina, A
    Benson, SC
    Pershadsingh, HA
    Chuck, RS
    EXPERIMENTAL EYE RESEARCH, 2005, 80 (03) : 435 - 442
  • [24] Peroxisome proliferator-activated receptor-α regulates postischemic liver injury
    Okaya, T
    Lentsch, AB
    AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2004, 286 (04): : G606 - G612
  • [25] Peroxisome proliferator-activated receptor-γ protects against vascular aging
    Modrick, Mary L.
    Kinzenbaw, Dale A.
    Chu, Yi
    Sigmund, Curt D.
    Faraci, Frank M.
    AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2012, 302 (10) : R1184 - R1190
  • [26] Flexible ligand recognition of peroxisome proliferator-activated receptor-γ (PPARγ)
    Yamagishi, Kenji
    Yamamoto, Keiko
    Mochizuki, Yuji
    Nakano, Tatsuya
    Yamada, Sachiko
    Tokiwa, Hiroaki
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2010, 20 (11) : 3344 - 3347
  • [27] Peroxisome proliferator-activated receptor-α accelerates α-chlorofatty acid catabolism
    Palladino, Elisa N. D.
    Wang, Wen-yi
    Albert, Carolyn J.
    Langhi, Cedric
    Baldan, Angel
    Ford, David A.
    JOURNAL OF LIPID RESEARCH, 2017, 58 (02) : 317 - 324
  • [28] Peroxisome proliferator-activated receptor-/ modulates mast cell phenotype
    Yao, Pei-Li
    Morales, Jose L.
    Gonzalez, Frank J.
    Peters, Jeffrey M.
    IMMUNOLOGY, 2017, 150 (04) : 456 - 467
  • [29] Targeting Peroxisome Proliferator-Activated Receptor-β/δ (PPARβ/δ) for Cancer Chemoprevention
    Peters J.M.
    Yao P.-L.
    Gonzalez F.J.
    Current Pharmacology Reports, 2015, 1 (2) : 121 - 128
  • [30] Selective peroxisome proliferator-activated receptor-α modulator K-877 efficiently activates the peroxisome proliferator-activated receptor-α pathway and improves lipid metabolism in mice
    Takei, Kenta
    Han, Song-iee
    Murayama, Yuki
    Satoh, Aoi
    Oikawa, Fusaka
    Ohno, Hiroshi
    Osaki, Yoshinori
    Matsuzaka, Takashi
    Sekiya, Motohiro
    Iwasaki, Hitoshi
    Yatoh, Shigeru
    Yahagi, Naoya
    Suzuki, Hiroaki
    Yamada, Nobuhiro
    Nakagawa, Yoshimi
    Shimano, Hitoshi
    JOURNAL OF DIABETES INVESTIGATION, 2017, 8 (04) : 446 - 452