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Surgical Colic Congestion in a Constipation Model in Rats

Autor: M. Tsivian, G. L. Piras, M. Pariali, R. Aldini, NERI, FLAVIA, BIANCHI, ELISA, CAVALLARI, GIUSEPPE, BERTELLI, RICCARDO, BELTEMPO, PAOLO, NARDO, BRUNO

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______4094::744d8a85808dcf2c9f847fe09c9e48bc
http://hdl.handle.net/11585/128443

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Congestione venosa colica indotta chirurgicamente in un modello di stipsi farmacologica nel ratto

Autor: M. Tsivian, GL Piras, D. Prezzi, M. Pariali, R. Aldini, NERI, FLAVIA, PUVIANI, LORENZA, BERTELLI, RICCARDO, CAVALLARI, GIUSEPPE, NARDO, BRUNO

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______4094::31d68c5ea94694a15e7240afe1fcd65d
http://hdl.handle.net/11585/128300

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Akademický článek

Hepatic bile acid uptake: effect of conjugation, hydroxyl and keto groups, and albumin binding

Autor: R Aldini, A Roda, A M Labate, G Cappelleri, E Roda, L Barbara

Publikováno v: Journal of Lipid Research, Vol 23, Iss 8, Pp 1167-1173 (1982)

Hepatic extraction of trihydroxy (free, glyco- and tauro-conjugated) dihydroxy, and monohydroxy bile acids has been evaluated in single pass liver perfusion experiments in rats. The percentage of each bile acid bound to albumin was also evaluated by

Externí odkaz: https://doaj.org/article/0c3f8edd28354ebc9adf5d836c6f4ffa

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Akademický článek

Quantitative aspects of the interaction of bile acids with human serum albumin.

Autor: A Roda, G Cappelleri, R Aldini, E Roda, L Barbara

Publikováno v: Journal of Lipid Research, Vol 23, Iss 3, Pp 490-495 (1982)

The interaction of human serum albumin with twelve bile acids (ba) has been studied by equilibrium dialysis technique using 3H- and 14C-labeled bile acids. The physiological bile acids studied were: cholic, chenodeoxycholic, deoxycholic, lithocholic,

Externí odkaz: https://doaj.org/article/3df65693831545d48e37cb71708b81ba

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Akademický článek

Bile acids with a cyclopropyl-containing side chain. IV. Physicochemical and biological properties of the four diastereoisomers of 3 alpha,7 beta-dihydroxy-22,23-methylene-5 beta-cholan-24-oic acid.

Autor: A Roda, B Grigolo, R Aldini, P Simoni, R Pellicciari, B Natalini, R Balducci

Publikováno v: Journal of Lipid Research, Vol 28, Iss 12, Pp 1384-1397 (1987)

To define the influence of the side chain modification on physicochemical and biological properties of bile acids, 3 alpha,7 beta-dihydroxy-22,23-methylene-5 beta-cholan-24-oic acid, a cyclopropyl analog of ursodeoxycholic acid (UDCA) was synthesized

Externí odkaz: https://doaj.org/article/21f1303b6256455793560576376f7768

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