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J.-P. Laigneau

Researcher at French Institute of Health and Medical Research

Publications -  21
Citations -  2071

J.-P. Laigneau is an academic researcher from French Institute of Health and Medical Research. The author has contributed to research in topics: Leptin & Leptin receptor. The author has an hindex of 13, co-authored 21 publications receiving 2018 citations.

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The stomach is a source of leptin

TL;DR: It is shown that leptin messenger RNA and leptin protein are present in rat gastric epithelium, and that cells in the glands of the gastric fundic mucosa are immunoreactive for leptin, indicating that gastric leptin may be involved in early CCK-mediated effects activated by food intake, possibly including satiety.
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Leptin secretion and leptin receptor in the human stomach

TL;DR: These data provide the first evidence of the presence of leptin and leptin receptor proteins in the human stomach and suggest that gastric epithelial cells may be direct targets for leptin.
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Leptin stimulates the proliferation of human colon cancer cells in vitro but does not promote the growth of colon cancer xenografts in nude mice or intestinal tumorigenesis in Apc(Min/+) mice.

TL;DR: The findings do not support a pivotal role for hyperleptinaemia in intestinal carcinogenesis and leptin acts as a growth factor on colon cancer cells in vitro but does not promote tumour growth in vivo in the two models tested.
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Leptin reduces the development of the initial precancerous lesions induced by azoxymethane in the rat colonic mucosa.

TL;DR: This study provides the first evidence that leptin reduces the development of chemically induced precancerous lesions in colon, perhaps through decreased insulinemia, and thus does not support an important role for leptin in carcinogenesis promotion.
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Physiological role of cholecystokinin B/gastrin receptor in leptin secretion.

TL;DR: Data argue for a physiological role for the cholecystokinin or its structurally related peptide gastrin in long term regulation of adipocyte leptin secretion, and suggest a role for gastrin/CCK-B receptor mRNA, but not CCK-A receptor mRNA.