Evaluation of the relaxant effect of levetiracetam on isolated rat duodenum

2016 ◽  
Vol 31 (1) ◽  
pp. 75-82 ◽  
Author(s):  
Hesham A. Salem ◽  
Muhammad Y. Al-Shorbagy
2021 ◽  
Vol 4 (2) ◽  
pp. 01-05
Author(s):  
Mirzayeva Yu.T.

The aim of our research is to study the effect relaxant action of diterpenoid alkaloids talatisamine, 14-O-benzoylthalatisamine and 14-O-acetylthalatisamine was studied using isolated rat aortic rings. Alkaloids significantly and dose-dependently inhibited contraction of the aortic rings caused by high KCl content. At the same time, under these conditions, alkaloids significantly reduced Ca2+-induced contraction of the aortic rings. The relaxing effects of alkaloids are significantly suppressed by verapamil, a potent potentiometer-dependent Ca2+ channel blocker. The alkaloids also significantly reduced norepinephrine-induced aortic ring contraction in normal as well as Ca2+ free Krebs solutions. The data obtained indicate that talatisamine, 14-benzoylthalatisamine and 14-O-acetylthalatisamine exhibit a pronounced relaxant effect in almost the same way in the case of contraction induced by a high content of KCl and norepinephrine. The mechanism of the relaxant action of alkaloids is probably complex and may include suppression of Ca2+influx through voltage-dependent and receptor-driven Ca2+ channels, as well as inhibition of Ca2+transport in the sarcoplasmic reticulum.


2002 ◽  
Vol 365 (3) ◽  
pp. 187-192 ◽  
Author(s):  
Emilia Nocerino ◽  
Angelo Izzo ◽  
Francesca Borrelli ◽  
Francesco Capasso ◽  
Raffaele Capasso ◽  
...  

1988 ◽  
Vol 19 (5) ◽  
pp. 655-659 ◽  
Author(s):  
C.R.C. Guimaraes ◽  
L.A. Rodrigues ◽  
O. Vettore ◽  
A. Antonio

1995 ◽  
Vol 275 (1) ◽  
pp. 45-51 ◽  
Author(s):  
Kaoru Irie ◽  
Yoko Uchida ◽  
Emiko Fujii ◽  
Takamura Muraki

Molecules ◽  
2010 ◽  
Vol 15 (5) ◽  
pp. 3391-3401 ◽  
Author(s):  
Dubravka Bigovic ◽  
Suzana Brankovic ◽  
Dusanka Kitic ◽  
Mirjana Radenkovic ◽  
Teodora Jankovic ◽  
...  

2006 ◽  
Vol 34 (04) ◽  
pp. 655-665 ◽  
Author(s):  
Dae Gill Kang ◽  
Li Hua Cao ◽  
Jun Kyoung Lee ◽  
Deok Ho Choi ◽  
Seung Ju Kim ◽  
...  

The butanol extract of Phellinus igniarius (BPI) induced relaxation of the phenylephrin e-precontracted rat aorta in a dose-dependent manner, and its effect was abolished by the removal of functional endothelium. Pretreatment of the aortic tissues with NG -nitro-L-arginine methyl ester (L-NAME), methylene blue, or 1H-[1,2,4]-oxadiazole-[4,3-α]-quinoxalin1-one (ODQ) inhibited the vascular relaxation induced by BPI. BPI-induced vascular relaxations were also markedly attenuated by the addition of verapamil or diltiazem, while the relaxant effect of BPI was not blocked by pretreatment with indomethacine, glibenclamide, tetraethylammonium (TEA), atropine, or propranolol. Incubation of endothelium-intact rat aorta with BPI increased the production of cGMP in a dose-dependent manner. These results suggest that BPI dilates vascular smooth muscle via endothelium-dependent nitric oxide-cGMP signaling pathway, with the possible involvement of L-type Ca 2+ channels.


2019 ◽  
Vol 97 (5) ◽  
pp. 413-421 ◽  
Author(s):  
Deniz Kaleli-Durman ◽  
F. İlkay Alp-Yıldırım ◽  
Osman Özdemir ◽  
B. Sönmez Uydeş-Doğan

Statins are determined to have various pleiotropic effects apart from their lipid-lowering properties. Herein, we investigated the direct effects of atorvastatin on gastric smooth muscle tone. Atorvastatin effectively relaxed isolated rat gastric fundus strips precontracted with acetylcholine, potassium chloride, and serotonin. Incubation of the strips with nitric oxide synthase inhibitor, l-NOARG (10−4 M, 20 min), l-type voltage-operated Ca2+ channel (VOCC) blocker, nifedipine (10−6 M, 30 min), KATP channel blocker, glibenclamide (10−5 M, 30 min), or precursor of cholesterol, mevalonate (10−2 M, 45 min) did not change the relaxations to atorvastatin. However, pretreatment of fundus strips with atorvastatin (3×10−5–3×10−4 M, 30 min) inhibited the contractions to calcium chloride (10−4–10−1 M), acetylcholine (10–4 M), and caffeine (20 mM) in the calcium-free medium. Moreover, atorvastatin reduced the contractions induced by sarco-endoplasmic reticulum Ca2+-ATPase (SERCA) inhibitor, cyclopiazonic acid (10−7–3×10−5 M). The current study demonstrated that atorvastatin produces an acute relaxant effect on gastric fundus strips, which appears to be mediated by several Ca2+-signalling mechanisms such as the blockade of l-type VOCC-independent Ca2+ entry, decrease in smooth muscle Ca2+ sensitivity, inhibition of IP3- and ryanodine-sensitive intracellular stores to mediate Ca2+ release, as well as the activation of SERCA. This acute relaxing effect seems unlikely to be related with nitric oxide, KATP channels, and the mevalonate pathway.


2004 ◽  
Vol 67 (6) ◽  
pp. 1203-1214 ◽  
Author(s):  
Karel Chalupsky ◽  
Irina Lobysheva ◽  
Françoise Nepveu ◽  
Irina Gadea ◽  
Petra Beranova ◽  
...  

2015 ◽  
Vol 172 ◽  
pp. 1-9 ◽  
Author(s):  
Njiaza Joseph ◽  
Ngo Lemba Tom Esther ◽  
Nguelefack Télesphore Benoît ◽  
Dzeufiet Djomeni Paul Désiré ◽  
Aboubakar Oumarou Bibi-Farouck ◽  
...  

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