Vasorelaxant effect of isopropyl 3-(3, 4-dihydroxyphenyl)-2-hydroxypropanoate, a novel metabolite from Salvia miltiorrhiza, on isolated rat mesenteric artery

2008 ◽  
Vol 579 (1-3) ◽  
pp. 283-288 ◽  
Author(s):  
Sheng-Peng Wang ◽  
Wei-Jin Zang ◽  
Shan-Shan Kong ◽  
Xiao-Jiang Yu ◽  
Lei Sun ◽  
...  
Author(s):  
Tays Amanda Felisberto Gonçalves ◽  
Renildo Moura da Cunha ◽  
Dionatas Ulises de Oliveira Meneguetti ◽  
Marcio Roberto Viana Santos ◽  
José Maria Barbosa- Filho ◽  
...  

Aims: To evaluate the vasorelaxant effect induced by the essential oil of the leaves of O. duckei Vattimo (ODEO) and its main constituent, trans-caryophyllene, in rat superior mesenteric arteries. Methodology: Isolated rat superior mesenteric rings were suspended by cotton threads for isometric tension recordings in Tyrode’s solution at 37ºC, gassed with 95% O2 and 5% CO2 and different ODEO concentrations (0.1-300 μg/mL) or trans-caryophyllene (1-1000 μg/mL) were added cumulatively to the organ baths. Results: Vasorelaxant effect induced by the essential oil of Ocotea duckei leaves (ODEO) and its main constituent, trans-caryophyllene (60.54 %), was evaluated in this work. In intact isolated rat superior mesenteric rings ODEO (0.1-300 μg/mL, n=6) induced concentration-dependent relaxation of tonus induced by phenylephrine (10 µM) or K+-depolarizing solution (KCl 80 mM) (IC50=31±5, 5±0.4 µg/mL, respectively, n=6). The relaxations of phenylephrine-induced contractions were not significantly attenuated after removal of the vascular endothelium (IC50=25±5 µg/mL). ODEO antagonized the concentration-response curves to CaCl2 (10-6-3x10-2 M) and Bay K 8644 (10-10-3x10-6 M). Furthermore, in nominally without calcium solution, ODEO significantly inhibited, in a concentration-dependent manner, transient contractions induced by 10 µM phenylephrine or 20 µM caffeine. Trans-caryophyllene induced vasorelaxations, however, this effect was 18.6 times less potent when compared to ODEO-induced vasorelaxations. Conclusion: The relaxant effect induced by ODEO in rat superior mesenteric artery rings is endothelium-independent and seems to be related to both, inhibition of Ca2+ influx through L-type voltage-gated Ca2+-channels sensitive to dihydropyridines and inhibition of the calcium release from intracellular IP3-and caffeine-sensitive stores.


2014 ◽  
Vol 28 (12) ◽  
pp. 923-927 ◽  
Author(s):  
Daniel Dias Rufino Arcanjo ◽  
Joaquim Soares da Costa-Júnior ◽  
Lucas Henrique Porfírio Moura ◽  
Alexandre Barros Falcão Ferraz ◽  
Raíssa Rebés Rossatto ◽  
...  

1998 ◽  
Vol 32 (4) ◽  
pp. 405-410 ◽  
Author(s):  
Bernard L Lopez ◽  
Jack W Snyder ◽  
Dale S Birenbaum ◽  
Xin-liang Ma

2020 ◽  
Vol 21 (17) ◽  
pp. 6392
Author(s):  
Emma D. Flood ◽  
Stephanie W. Watts

Background: We previously reported that the adipokine chemerin, when added exogenously to the isolated rat mesenteric artery, amplified electrical field-stimulated (EFS) contraction. The Chemerin1 antagonist CCX832 alone inhibited EFS-induced contraction in tissues with but not without perivascular adipose tissue (PVAT). These data suggested indirectly that chemerin itself, presumably from the PVAT, facilitated EFS-induced contraction. We created the chemerin KO rat and now test the focused hypothesis that endogenous chemerin amplifies EFS-induced arterial contraction. Methods: The superior mesenteric artery +PVAT from global chemerin WT and KO female rats, with endothelium and sympathetic nerve intact, were mounted into isolated tissue baths for isometric and EFS-induced contraction. Results: CCX832 reduced EFS (2–20 Hz)-induced contraction in tissues from the WT but not KO rats. Consistent with this finding, the magnitude of EFS-induced contraction was lower in the tissues from the KO vs. WT rats, yet the maximum response to the adrenergic stimulus PE was not different among all tissues. Conclusion: These studies support that endogenous chemerin modifies sympathetic nerve-mediated contraction through Chemerin1, an important finding relative in understanding chemerin’s role in control of blood pressure.


2010 ◽  
Vol 20 (5) ◽  
pp. 762-765 ◽  
Author(s):  
Ítalo J. A. Moreira ◽  
Maria P. N. Moreno ◽  
Maria F. G. Fernandes ◽  
João B. Fernandes ◽  
Flávia V. Moreira ◽  
...  

2011 ◽  
Vol 60 (04) ◽  
pp. 189-197
Author(s):  
Radica Stepanović-Petrović ◽  
Vladimir Savić ◽  
Maja Tomić ◽  
Zorana Tokic-Vujošević ◽  
Milena Simić ◽  
...  

1991 ◽  
Vol 177 (3) ◽  
pp. 1127-1132 ◽  
Author(s):  
Kazuhiro Hisaki ◽  
Yasuo Matsumura ◽  
Ruriko Ikegawa ◽  
Sumika Nishiguchi ◽  
Kazutaka Hayashi ◽  
...  

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