Czasopismo
Tytuł artykułu
Autorzy
Warianty tytułu
Języki publikacji
Abstrakty
In this paper, BV-2 mouse small glial cell inflammation model induced by LPS is established. The experiment used 0.1-10 μM of telmisartan and Tek-1 to incubate with small glial cell and used telmisartan and Tek-1 to incubate with PPAR gamma special heterosexual antagonistic anti-agent GW9662. The article used ELISA method to dectect TNF-a effect on small glial cell for telmisartan and Tek-1. The article used real-time quantitative PCR method to dectect mRNA level expression effect of CD11b, CD16 and iNOS on small glial cell for telmisartan and Tek-1 and used Western Blot method to dectect MAPKs signal pathway and NF-κb signal turned guide pathway effect on small glial cell for telmisartan and Tek-1. Results show that Tek-1 had high affinity with AT1 receptor and inhibited intracellular calcium ion activation which can be for the AT1 receptor antagonists. Meanwhile, Tek-1 can partially activate PPAR gamma compared with full agonists of rosiglitazone.
Słowa kluczowe
Czasopismo
Rocznik
Tom
Numer
Opis fizyczny
Daty
wydano
2015-01-01
otrzymano
2015-07-10
zaakceptowano
2015-10-14
online
2015-12-17
Twórcy
autor
- Department of Neurology, Xian Jiao Tong University, Postal code 710061, China, 706329630@qq.com
autor
- Department of Vasculocardiology, Xian Jiao Tong University, Postal code 710061, China
Bibliografia
- [1] Cameron B., Landreth G.E., Inflammation, microglia, and Alzheimer’s disease, Neurobiol Dis., 2010, 37(3), 503-509[WoS][Crossref]
- [2] Lue L.F., et al., Microglia activation and anti-inflammatory regulation in Alzheimer’s disease, Mol. Neurobiol., 2010, 41(2-3), 115-128[WoS][Crossref]
- [3] Joglar B., Rodriguez-Pallares J., et al., The inflammatory response in the MPTP model of Parkinson’s disease is mediated by brain angiotensin: relevance to progression of the disease, J. Neurochem., 2009, 109, 656-669[WoS]
- [4] Lu Q., Zhu Y.Z., et al., Neuroprotective effects of candesartan against cerebral ischemia in spontaneously hypertensive rats, Neuroreport, 2005, 16, 1963-1967
- [5] Jung W.K., et al., Cilostazol is anti-inflammatory in BV2 microglial cells by inactivating nuclear factor-kappaB and inhibiting mitogen-activated protein kinases, Br. J. Pharmacol., 2010, 159(6), 1274-1285[WoS]
- [6] Nagai Y., Akashi S., et al., Essential role of MD-2 in LPS responsiveness and TLR4 distribution, Nat. Immunol., 2002, 3(7), 667-672
- [7] Storer P.D., et al., Peroxisome proliferator-activated receptor-gamma agonists inhibit the activation of microglia and astrocytes: implications for multiple sclerosis, J. Neuroimmunol., 2005, 161(1-2), 113-122
- [8] Wang Y., et al., T33 a novel peroxisome proliferator-activated receptor gamma/alpha agonist, exerts neuroprotective action via its anti-inflammatory activities, Act. Pharmacol. Sin., 2011, 32(9), 1100-1108[Crossref]
- [9] Garrido-Gil, et al., Involvement of PPAR-γ in the Neuroprotective and anti-inflammatory effects of angiotensin type 1 receptor inhibition: effects of the receptor antagonist telmisartan and receptor deletion in a mouse MPTP model of Parkinson’s disease, Journal of Neuroinflammation, 2012, 9, 38[WoS]
- [10] Xiao J., Leung J.C., et al., Crosstalk between peroxisome proliferator-activated receptor-gamma and angiotensin II in renal tubular epithelial cells in IgA nephropathy, Clin. Immunol., 2009, 132, 266-276[WoS]
- [11] Pacher P., Beckman J.S., et al., Nitric oxide and peroxynitrite in health and disease, Physiol. Rev., 2007, 87(1), 315-424[Crossref][WoS]
- [12] Aloisi F., Immune function of microglia, Glia, 2001, 36(2), 165-179[Crossref]
- [13] Pearson Q., Beers G.T., et al., Mitogen-activated protein (MAP) kinase pathways: regulation and physiological functions, Endocr. Rev., 2001, 22(2), 153-183
- [14] Chow Y.L., et al., Cardamom from Alpena rafflesiana inhibits inflammatory responses in IFN-gamma/LPS-stimulated BV2 microglia via NF-kappaB signaling pathway, Int. Immunopharmacol, 2012, 12(4), 657-65[Crossref]
Typ dokumentu
Bibliografia
Identyfikatory
Identyfikator YADDA
bwmeta1.element.-psjd-doi-10_1515_med-2015-0077