Comparative effect of glucagon, dibutyryl cyclic AMP, and epinephrine on the desaturation and elongation of linoleic acid by rat liver microsomes
The effect of glucagon, dibutyryl cyclic adenosine 3′,5′-monophosphate, and epinephrine on the biosynthesis of polyunsaturated fatty acids of the linoleic acid family was studied. The incubations were performed with rat liver microsomes and labeled linoleic acid under desaturating and elongating con...
Autores principales: | , , |
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Formato: | Articulo |
Lenguaje: | Inglés |
Publicado: |
1976
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Materias: | |
Acceso en línea: | http://sedici.unlp.edu.ar/handle/10915/140098 |
Aporte de: |
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I19-R120-10915-140098 |
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record_format |
dspace |
institution |
Universidad Nacional de La Plata |
institution_str |
I-19 |
repository_str |
R-120 |
collection |
SEDICI (UNLP) |
language |
Inglés |
topic |
Medicina Linoleic Acid Theophylline Glucagon Desaturation Activity Purina Chow |
spellingShingle |
Medicina Linoleic Acid Theophylline Glucagon Desaturation Activity Purina Chow Tacconi de Gómez Dumm, Irma Nelva Tacconi de Alaniz, María Josefa Brenner, Rodolfo Roberto Comparative effect of glucagon, dibutyryl cyclic AMP, and epinephrine on the desaturation and elongation of linoleic acid by rat liver microsomes |
topic_facet |
Medicina Linoleic Acid Theophylline Glucagon Desaturation Activity Purina Chow |
description |
The effect of glucagon, dibutyryl cyclic adenosine 3′,5′-monophosphate, and epinephrine on the biosynthesis of polyunsaturated fatty acids of the linoleic acid family was studied. The incubations were performed with rat liver microsomes and labeled linoleic acid under desaturating and elongating conditions. Under desaturating conditions, linoleic acid was converted to γ-linolenic acid, whereas under elongating conditions it was converted to 20∶2ω6. Glucagon, dibutyryl cyclic AMP, and epinephrine decreased the oxidative desaturation of linoleic acid to γ-linolenic acid while the elongating reaction was not modified in the experimental conditions tested. Consequently, the results support the hypothesis that the oxidative desaturation of linoleic acid to γ-linolenic acid is the main controllable step in the biosynthesis of polyunsaturated fatty acids of the linoleic acid family in the microsomes. |
format |
Articulo Articulo |
author |
Tacconi de Gómez Dumm, Irma Nelva Tacconi de Alaniz, María Josefa Brenner, Rodolfo Roberto |
author_facet |
Tacconi de Gómez Dumm, Irma Nelva Tacconi de Alaniz, María Josefa Brenner, Rodolfo Roberto |
author_sort |
Tacconi de Gómez Dumm, Irma Nelva |
title |
Comparative effect of glucagon, dibutyryl cyclic AMP, and epinephrine on the desaturation and elongation of linoleic acid by rat liver microsomes |
title_short |
Comparative effect of glucagon, dibutyryl cyclic AMP, and epinephrine on the desaturation and elongation of linoleic acid by rat liver microsomes |
title_full |
Comparative effect of glucagon, dibutyryl cyclic AMP, and epinephrine on the desaturation and elongation of linoleic acid by rat liver microsomes |
title_fullStr |
Comparative effect of glucagon, dibutyryl cyclic AMP, and epinephrine on the desaturation and elongation of linoleic acid by rat liver microsomes |
title_full_unstemmed |
Comparative effect of glucagon, dibutyryl cyclic AMP, and epinephrine on the desaturation and elongation of linoleic acid by rat liver microsomes |
title_sort |
comparative effect of glucagon, dibutyryl cyclic amp, and epinephrine on the desaturation and elongation of linoleic acid by rat liver microsomes |
publishDate |
1976 |
url |
http://sedici.unlp.edu.ar/handle/10915/140098 |
work_keys_str_mv |
AT tacconidegomezdummirmanelva comparativeeffectofglucagondibutyrylcyclicampandepinephrineonthedesaturationandelongationoflinoleicacidbyratlivermicrosomes AT tacconidealanizmariajosefa comparativeeffectofglucagondibutyrylcyclicampandepinephrineonthedesaturationandelongationoflinoleicacidbyratlivermicrosomes AT brennerrodolforoberto comparativeeffectofglucagondibutyrylcyclicampandepinephrineonthedesaturationandelongationoflinoleicacidbyratlivermicrosomes |
bdutipo_str |
Repositorios |
_version_ |
1764820458261184512 |