21 research outputs found
Preclinical students’ experiences in early clerkships after skills training partly offered in primary health care centers: a qualitative study from Indonesia
Effects of Different Selenium Levels on Gene Expression of a Subset of Selenoproteins and Antioxidative Capacity in Mice
PHARMACOLOGICAL PROPERTIES OF MM-706, A NEW PROSTACYCLIN DERIVATIVE
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1. In human platelet-rich plasma, platelet aggregation induced in vitro by collagen (10 \u3bcg/ml) or thrombin (50 mU/ml) was dose-dependently inhibited by increasing concentrations of prostacyclin or of the new derivative (\ub1)(5E)-13,14-didehydro-\u3c9-hexanor(1-hydroxycyclohexyl)-9a-carbaprostacyclin (MM-706) with an IC50 of 20\u201350 nM and 250\u2013500 nM, respectively. In human platelets loaded with fura-2, the intracellular rise of [Ca2+] induced by thrombin was dose-dependently inhibited by MM-706 with an approximate IC50 of 100 \u3bcM.
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2. In rabbit isolated femoral artery, MM-706 (10nM\u201310\u3bcM) was completely ineffective in relaxing the vessel, which was different to prostacyclin which was able to relax vessels at the same concentrations.
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3. In in vitro guinea-pig ileum, prostacyclin produced a contractile effect in the concentration range 1 nM-10\u3bcM, but the derivative MM-706 was ineffective at the same concentrations. Preventive addition of MM-706 did not inhibit prostacyclin contraction.
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4. On isolated guinea-pig tracheal preparation, prostacyclin induced a concentration-dependent contraction but the new compound MM-706 showed a lower activity, in the concentration range 10nM\u201310\u3bcM. The activity of prostacyclin was not affected by the contemporary presence of MM-706.
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5. It is concluded that MM-706 is a prostacyclin analogue with antiaggregating properties but without evident effects on smooth muscle of different regions