2021
DOI: 10.4254/wjh.v13.i11.1611
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Newly discovered endocrine functions of the liver

Abstract: The liver, the largest solid visceral organ of the body, has numerous endocrine functions, such as direct hormone and hepatokine production, hormone metabolism, synthesis of binding proteins, and processing and redistribution of metabolic fuels. In the last 10 years, many new endocrine functions of the liver have been discovered. Advances in the classical endocrine functions include delineation of mechanisms of liver production of endocrine hormones [including 25-hydroxyvitamin D, insulin-like growth factor 1 … Show more

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Cited by 28 publications
(15 citation statements)
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“…Thus, besides direct effects on GLP-1, quinoa with saponin may play a key role on GLP-1 via regulation of TGR5 and gut microbiome. GLP-1 is also expressed in the liver and can function as an important factor in the gut-liver axis ( 32 ). Besides, GLP-1 exists in the brain and the sources of GLP-1 in brains may be circulating GLP-1 or GLP-1 produced in the brain or peripheral GLP-1 via vagal afferents.…”
Section: Discussionmentioning
confidence: 99%
“…Thus, besides direct effects on GLP-1, quinoa with saponin may play a key role on GLP-1 via regulation of TGR5 and gut microbiome. GLP-1 is also expressed in the liver and can function as an important factor in the gut-liver axis ( 32 ). Besides, GLP-1 exists in the brain and the sources of GLP-1 in brains may be circulating GLP-1 or GLP-1 produced in the brain or peripheral GLP-1 via vagal afferents.…”
Section: Discussionmentioning
confidence: 99%
“…Systemic minocycline therapy has been linked with hepatoxicity, nephritis, and thyroid dysfunction, leading to adverse effects on host health ( 55 – 58 ). Importantly, liver, kidney, and thyroid function regulate skeletal metabolism ( 55 , 59 61 ). Histopathology studies did not detect minocycline-induced toxicity effects in the kidney or liver of male SPF mice ( Figure 3F ).…”
Section: Resultsmentioning
confidence: 99%
“…AA's increase is involved in a-cell proliferation particularly through glutamine, which is transported in a-cells through Slc38a5 (AA transporter) and, which increases mTOR expression involved in a-cell proliferation (145,146). This glutamine-dependent a-cell proliferation re-establishes the production of glucagon and, so hepatic glucose's production (147). Thus, this axis presents several target for diabetes' therapies (146).…”
Section: Hepatic/a-cells Axismentioning
confidence: 99%