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veratrine/veratrum

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ČlankiKliničnih preskušanjPatenti
14 rezultatov

[Accessory alkaloids of sabadilla. VIII. Veratrine-veratrum alkaloids].

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Studies on Veratrum alkaloids. XXV. Veratrine response and antiveratrinic action in frog sartorius muscle.

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[Isomeric forms of germine. 5. Veratrine Veratrum alkaloid].

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[Hydration products of veratrine-alkamines. 6. Veratrine-Veratrum alkaloids].

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[Veratrine-Veratrum alkaloids. IX. Neosabadin, a new Sabadilla alkamine].

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[Contribution to the knowledge of various veratrum drugs and their alkaloids. VII. Veratrine-veratrum-alkaloids].

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The veratrine alkaloids; the alkaloids of Veratrum viride.

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Lack of cross-tolerance between disodium cromoglycate and veratrum alkaloids.

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We sought to determine if the hypotension and bradycardia caused by disodium cromoglycate (DSC) and veratrine sulfate were due to an action upon a common receptor. Tolerance rapidly developed to the hypotensive and bradycardic action of 10 micrograms/kg iv DSC in anesthetized dogs. Veratrine sulfate

Muscarinic acetylcholine receptors in neuroblastoma cells: lack of effect of Veratrum alkaloids on receptor number.

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The effect of compounds that activate sodium channels on the number of muscarinic acetylcholine receptors in neuroblastoma NIE 115 cells has been investigated. The cells were used in electrically unexcitable ("control" cells) and excitable ("differentiated" cells) states. Although receptor assays

Effects of nerve stimulation on ion transport in mouse jejunum: responses to Veratrum alkaloids.

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Veratrum alkaloids were used to examine the effect of neural stimulation on intestinal ion transport in full-thickness (intact) and serosally stripped (mucosal) preparations of mouse jejunum. When applied to the serosal media of mucosal preparations, veratrine or veratridine evoked a biphasic
Cardiovascular responses to intravenous bolus doses of certain exogenous substances (capsaicin, phenyldiguanide, cryptenamine, veratrine sulphate) which act on chemoreceptors in the pulmonary or proximal arterial circulation were compared to the naturally occurring chemoreceptor agonist,
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