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Pregled bibliografske jedinice broj: 821402

Effect of tempol in vivo on flow-induced dilation in vitro in middle cerebral arteries of healthy Sprague-Dawley rats


Ćosić, Anita; Unfirer, Sanala; Jukić, Ivana; Stupin, Ana; Drenjančević, Ines
Effect of tempol in vivo on flow-induced dilation in vitro in middle cerebral arteries of healthy Sprague-Dawley rats // ESCHM 2016 Abstract Book
Lisabon, Portugal, 2016. (poster, međunarodna recenzija, sažetak, znanstveni)


Naslov
Effect of tempol in vivo on flow-induced dilation in vitro in middle cerebral arteries of healthy Sprague-Dawley rats

Autori
Ćosić, Anita ; Unfirer, Sanala ; Jukić, Ivana ; Stupin, Ana ; Drenjančević, Ines

Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni

Izvornik
ESCHM 2016 Abstract Book / - , 2016

Skup
18th Conference of the European Society for Clinical Hemorheology and Microcirculation

Mjesto i datum
Lisabon, Portugal, 05-08.06.2016

Vrsta sudjelovanja
Poster

Vrsta recenzije
Međunarodna recenzija

Ključne riječi
Oxidative stress; flow induced dilation; cerebral arteries

Sažetak
OBJECTIVE: This study aimed to determine if in vivo scavenging of superoxide by TEMPOL influences the mechanisms of flow-induced dilation (FID) of middle cerebral arteries (MCA) in vitro. DESIGN AND METHODS: 11-weeks old healthy male Spraque-Dawley (SD) rats (N=10-16) were given drinking water (control group) or 1 nM/L of TEMPOL in drinking water (TEMPOL group) for 7 days. FID (response to stepwise increase in pressure gradient (Δ10-Δ100 mmHg)) was determined in isolated, pressurized MCA in the absence/presence of the NOS inhibitor L- NAME, COX-1, 2 inhibitor indomethacin (INDO), CYP450 epoxidase inhibitor MS-PPOH. Cu/Zn SOD, MnSOD, EC-SOD, COX 1, 2, GPx4 and catalase mRNA levels were determined by real- time qPCR from brain blood vessels (N=5-8). All experimental procedures were approved by the local Ethical Committee and conformed to the EU Directive 86/609. RESULTS: FID (no inhibitors) was similar between groups (p>0.05). FID was similarly affected byinhibitors in both groups. TEMPOL significantly upregulated Cu/Zn- and MnSODs and COX1, while downregulated COX2 genes compared to control. In control group MnSOD positively correlated to COX1 (r=0.802, p=0.05) and GPx1 (r=0.904, p=0.01). In TEMPOL group, Cu/ZnSOD positively correlated to GPx1 (r=0.979, p=0.004), while MnSOD positively correlated to COX2 (r=0.859, p=0.029). CONCLUSIONS: TEMPOL affected the expression of COX and SOD isoforms, which may be accountable for preserved FID.

Izvorni jezik
Engleski

Znanstvena područja
Temeljne medicinske znanosti



POVEZANOST RADA


Ustanove
Medicinski fakultet, Osijek