Literature DB >> 22734567

Light-dark cycle and feeding time differentially entrains the gut molecular clock of the goldfish (Carassius auratus).

Laura G Nisembaum1, Elena Velarde, Ana B Tinoco, Clara Azpeleta, Nuria de Pedro, Angel L Alonso-Gómez, María J Delgado, Esther Isorna.   

Abstract

The aim of the present study was to investigate how photocycle and feeding-time cues regulate the daily expression of Per1a, Per2a, Per3, and Cry3 in the goldfish hindgut. For this purpose, we studied the daily rhythmicity of these genes in fish maintained under different lighting conditions and under different feeding regimes (scheduled or not). We also studied whether the timing of just one meal is able to reset the hindgut molecular clock. In a first experiment, randomly fed fish were divided into four groups and kept under different light conditions for 30 d: 12 h light and 12 h dark (12L:12D), an inverted photoperiod (12D:12L), constant darkness (24D), and constant light (24L). In a second study, fish maintained under 24L were divided into four groups fed at different time points for 35 d: (1) fish scheduled-fed once a day (at 10:00 h); (2) fish fed with a 12-h shifted schedule (at 22:00 h), (3) fish fed at 10:00 h throughout the experiment, except the last day when fed at 22:00 h; and (4) a randomly fed group of fish. Fish were sacrificed every 6 h throughout a 24-h cycle. In both experiments, gPer1a, gPer2a, gPer3, and gCry3 transcripts were quantified using Real Time-qPCR in the hindgut. Results show the clock genes gPer1a, gPer2a, and gCry3 are synchronized by both zeitgebers, the photocycle and feeding regime, in goldfish hindgut. Moreover, such clock genes anticipate light-on and food delivery, when these cues appear in a cyclic manner. In the absence of both zeitgebers, gCry3 and gPer2a rhythmicity disappeared. In contrast, the gPer1 rhythm was maintained under 24L and random feeding conditions, but not always, suggesting that food when randomly supplied is able to reset the clock depending on other factors, such as the energetic and metabolic conditions of the fish. The expression of gPer2a was not activated during the light phase of the cycle, suggesting the hindgut of goldfish is a non-direct photosensitive organ. In contrast to the other three genes, gPer3 expression in the goldfish hindgut seemed to be dependent on the timing of the last food delivery, even in the presence of a photocycle. This gene was the only one that maintained daily rhythms under both constant lighting conditions (24D and 24L), although with lower amplitude than when a photocycle was present. This indicates that, although the acrophase (peak time) of the gPer3 expression rhythm seems to be driven by feeding time, there is an interaction of both zeitgebers, food and light, to regulate its expression. In conclusion, present data indicate: (1) the hindgut of goldfish can be synchronized in vivo by both the photocycle and feeding time; (2) food is a potent signal that entrains this peripheral oscillator; and (3) both environmental cues seems to target different elements of the molecular clock.

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Year:  2012        PMID: 22734567     DOI: 10.3109/07420528.2012.686947

Source DB:  PubMed          Journal:  Chronobiol Int        ISSN: 0742-0528            Impact factor:   2.877


  9 in total

1.  Performing a hepatic timing signal: glucocorticoids induce gper1a and gper1b expression and repress gclock1a and gbmal1a in the liver of goldfish.

Authors:  Aída Sánchez-Bretaño; María Callejo; Marta Montero; Ángel L Alonso-Gómez; María J Delgado; Esther Isorna
Journal:  J Comp Physiol B       Date:  2015-10-03       Impact factor: 2.200

Review 2.  Rhythms in the endocrine system of fish: a review.

Authors:  Mairi Cowan; Clara Azpeleta; Jose Fernando López-Olmeda
Journal:  J Comp Physiol B       Date:  2017-04-26       Impact factor: 2.200

3.  Timed high-fat diet in the evening affects the hepatic circadian clock and PPARα-mediated lipogenic gene expressions in mice.

Authors:  Xiaoyan Wang; Jie Xue; Juan Yang; Meilin Xie
Journal:  Genes Nutr       Date:  2013-02-17       Impact factor: 5.523

4.  Nuclear Receptors (PPARs, REV-ERBs, RORs) and Clock Gene Rhythms in Goldfish (Carassius auratus) Are Differently Regulated in Hypothalamus and Liver.

Authors:  Miguel Gómez-Boronat; Nuria De Pedro; Ángel L Alonso-Gómez; María J Delgado; Esther Isorna
Journal:  Front Physiol       Date:  2022-06-06       Impact factor: 4.755

5.  Adjunctive agomelatine therapy in the treatment of acute bipolar II depression: a preliminary open label study.

Authors:  Michele Fornaro; Michael J McCarthy; Domenico De Berardis; Concetta De Pasquale; Massimo Tabaton; Matteo Martino; Salvatore Colicchio; Carlo Ignazio Cattaneo; Emanuela D'Angelo; Pantaleo Fornaro
Journal:  Neuropsychiatr Dis Treat       Date:  2013-02-15       Impact factor: 2.570

Review 6.  Hypothalamic Integration of Metabolic, Endocrine, and Circadian Signals in Fish: Involvement in the Control of Food Intake.

Authors:  María J Delgado; José M Cerdá-Reverter; José L Soengas
Journal:  Front Neurosci       Date:  2017-06-26       Impact factor: 4.677

7.  Harm of circadian misalignment to the hearts of the adolescent wistar rats.

Authors:  YunLei Wang; YuanYuan Hou; ShaoFei Song; Yao Zuo; Yan Yu; YaFei Chi; Tong Zhang
Journal:  J Transl Med       Date:  2022-08-06       Impact factor: 8.440

8.  In Situ Localization and Rhythmic Expression of Ghrelin and ghs-r1 Ghrelin Receptor in the Brain and Gastrointestinal Tract of Goldfish (Carassius auratus).

Authors:  Aída Sánchez-Bretaño; Ayelén M Blanco; Suraj Unniappan; Olivier Kah; Marie-M Gueguen; Juan I Bertucci; Ángel L Alonso-Gómez; Ana I Valenciano; Esther Isorna; María J Delgado
Journal:  PLoS One       Date:  2015-10-27       Impact factor: 3.240

9.  The Lack of Light-Dark and Feeding-Fasting Cycles Alters Temporal Events in the Goldfish (Carassius auratus) Stress Axis.

Authors:  Nuria Saiz; Miguel Gómez-Boronat; Nuria De Pedro; María Jesús Delgado; Esther Isorna
Journal:  Animals (Basel)       Date:  2021-03-03       Impact factor: 2.752

  9 in total

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