Tecoma stans is a plant traditionally used in Mexico for the control of diabetes. Amongst the alkaloids isolated from the plant harvested in Egypt, Tecomine was shown to be one of the compounds responsible for the hypoglycemic action. Given the interest in substances able to treat type II diabetes, we isolated the main alkaloids present in the plant growing in Egypt and Brazil and tested them in vivo on db/db mice. Contrary to previous literature reports on different animal models, Tecomine was unable to modify glycemia; the only effect seen being a decrease in plasma cholesterol levels. On the contrary, when tested in vitro on glucose uptake in white adipocytes, the compound showed a marked effect. The two other alkaloids isolated, namely 5beta-Hydroxyskitanthine, early called Base C, and Boschniakine were inactive both in vivo and in vitro assays.

Isolation and pharmacological activities of the Tecoma stans alkaloids / Costantino, L; Raimondi, L; Pirisino, R; Brunetti, T; Pessotto, P; Giannessi, F; Lins, Ap; Barlocco, D; Antolini, L; El-Abady, Sa.. - In: IL FARMACO. - ISSN 0014-827X. - ELETTRONICO. - 58:(2003), pp. 781-785.

Isolation and pharmacological activities of the Tecoma stans alkaloids.

Raimondi, L;PIRISINO, RENATO GIOVANNI PAOLO;
2003

Abstract

Tecoma stans is a plant traditionally used in Mexico for the control of diabetes. Amongst the alkaloids isolated from the plant harvested in Egypt, Tecomine was shown to be one of the compounds responsible for the hypoglycemic action. Given the interest in substances able to treat type II diabetes, we isolated the main alkaloids present in the plant growing in Egypt and Brazil and tested them in vivo on db/db mice. Contrary to previous literature reports on different animal models, Tecomine was unable to modify glycemia; the only effect seen being a decrease in plasma cholesterol levels. On the contrary, when tested in vitro on glucose uptake in white adipocytes, the compound showed a marked effect. The two other alkaloids isolated, namely 5beta-Hydroxyskitanthine, early called Base C, and Boschniakine were inactive both in vivo and in vitro assays.
2003
58
781
785
Costantino, L; Raimondi, L; Pirisino, R; Brunetti, T; Pessotto, P; Giannessi, F; Lins, Ap; Barlocco, D; Antolini, L; El-Abady, Sa.
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/1060145
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