dc.creator | Fonseca, Liza | |
dc.creator | Castillo, Valeska | |
dc.creator | Aguirre, Carolina | |
dc.creator | Silva, Paulo | |
dc.creator | Ronco, Ana M. | |
dc.creator | Llanos, Miguel | |
dc.date.accessioned | 2019-10-15T12:23:45Z | |
dc.date.available | 2019-10-15T12:23:45Z | |
dc.date.created | 2019-10-15T12:23:45Z | |
dc.date.issued | 2019 | |
dc.identifier | Journal of Nutrition and Metabolism, Volumen 2019, | |
dc.identifier | 20900732 | |
dc.identifier | 20900724 | |
dc.identifier | 10.1155/2019/2806519 | |
dc.identifier | https://repositorio.uchile.cl/handle/2250/171609 | |
dc.description.abstract | Several reports have shown that stress during lactation causes long-term metabolic and hormonal disruptions. In this study, we designed experiments to evaluate the effects of stress during lactation on the abundance of Type 1 cannabinoid/endocannabinoid receptors (CB1R) in epididymal fat and liver and development of insulin resistance in adult mice. During the whole lactation, male mice pups were daily subcutaneously injected (days 1-21) with a saline solution to produce a soft nociceptive stress (NS). Mice body weight and food intake were periodically evaluated. Adult animals were subsequently subjected to an insulin tolerance test and some days later sacrificed to evaluate the amount of epididymal fat and abundance of CB1R and adipophilin in liver and epididymal adipose tissue. Lipoprotein lipase (LPL) activity and circulating levels of leptin, adiponectin, and corticosterone were also evaluated. In this model, NS during lactation significantly increased th | |
dc.language | en | |
dc.publisher | Hindawi Limited | |
dc.rights | http://creativecommons.org/licenses/by-nc-nd/3.0/cl/ | |
dc.rights | Attribution-NonCommercial-NoDerivs 3.0 Chile | |
dc.source | Journal of Nutrition and Metabolism | |
dc.subject | Endocrinology, Diabetes and Metabolism | |
dc.subject | Food Science | |
dc.subject | Nutrition and Dietetics | |
dc.title | Stress during lactation induces insulin resistance associated with an increase in type 1 cannabinoid receptors in liver and adipose tissue | |
dc.type | Artículo de revista | |