“…Our results showed that PMAE partially but significantly inhibited in a concentration-dependent manner the contractile response elicited by carbachol or histamine on rat duodenum. Smooth muscles contraction, in response to histamine or carbachol is initiated by the increase of the cytoplasmic-free Ca 2 þ concentration.These agonists directly activate their specific receptors on the membrane of gastrointestinal smooth muscle cells (Rodriguez et al, 2006;Gilani et al, 2008), which results in activation of several intracellular pathways and production of second messengers (phospholipase C, inositol triphosphate, diacylglycerol, protein kinase C) which in turn stimulate the release of internal Ca 2 þ from sarcoplasmic reticulum stores and the Ca 2 þ influx through voltage-gated Ca 2 þ channels (Chiwororo et al, 2009;Desire et al, 2010;Dubravka et al, 2010;Hu et al, 2010). Therefore, the inhibitory effects of PMAE on carbachol-or histamine-induced contractions could be produced as a result of a blockage of muscarinic or histaminic receptors on the cell membrane, or a calcium channel blocking activity.…”