Dopaminergic D2 receptor knockout mouse: An animal model of prolactinoma
Dopamine receptor type 2 (D2R) knockout mice (KO) have chronic hyperprolactinemia, pituitary hyperplasia, and a moderate decrease in MSH content. They are also growth retarded evidencing an alteration in the GH-IGF-I axis. In D2R KO, lactotropes do not show dense secretory granules but degranulated...
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2006
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| Acceso en línea: | https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03013073_v35_n_p50_Cristina http://hdl.handle.net/20.500.12110/paper_03013073_v35_n_p50_Cristina |
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paper:paper_03013073_v35_n_p50_Cristina2023-06-08T15:27:53Z Dopaminergic D2 receptor knockout mouse: An animal model of prolactinoma dopamine 2 receptor vascular endothelial growth factor A, mouse vasculotropin A animal cell adhesion conference paper disease model drug resistance female genetics hyperplasia hypophysis hypophysis tumor male mouse mouse mutant neovascularization (pathology) pathology peliosis hepatis physiology prolactinoma sexual development vascularization Animals Cell Adhesion Disease Models, Animal Drug Resistance, Neoplasm Female Hyperplasia Male Mice Mice, Knockout Neovascularization, Pathologic Peliosis Hepatis Pituitary Gland Pituitary Neoplasms Prolactinoma Receptors, Dopamine D2 Sex Characteristics Vascular Endothelial Growth Factor A Dopamine receptor type 2 (D2R) knockout mice (KO) have chronic hyperprolactinemia, pituitary hyperplasia, and a moderate decrease in MSH content. They are also growth retarded evidencing an alteration in the GH-IGF-I axis. In D2R KO, lactotropes do not show dense secretory granules but degranulated cells and fewer somatotropes, gonadotropes and thyrotropes. Prolactin levels are always higher in female than in male knockouts, and in accordance, pituitary hyperplasia is observed at 8 months only in females. After 16 months of age, highly vascularized adenomas develop, especially in females. Prominent vascular channels in the hyperplastic and adenomatous pituitaries, as well as extravasated red blood cells not contained in capillaries is also a common finding. Prolactin is not the factor that enhances the hyperplastic phenotype in females while estrogen is a permissive factor. VEGF-A expression is increased in pituitaries from D2R KO. VEGF-A is expressed in follicle stellate cells. Because D2R receptors are found in lactotropes and not in follicle stellate cells, it may be inferred that a paracrine-derived factor from lactotropes is acting on follicle stellate cells to increase VEGF-A expression. VEGF-A does not induce pituitary cell proliferation, even though it enhances prolactin secretion. But it may act on adjacent endothelial cells and participate in the angiogenic process that increases the availability of different growth factors and mitogens. The D2R knockout mouse represents a unique animal model to study dopamine-resistant prolactinomas, and VEGF-A may be an alternative therapeutic target in this pathology. Copyright © 2006 S. Karger AG. 2006 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03013073_v35_n_p50_Cristina http://hdl.handle.net/20.500.12110/paper_03013073_v35_n_p50_Cristina |
| institution |
Universidad de Buenos Aires |
| institution_str |
I-28 |
| repository_str |
R-134 |
| collection |
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) |
| topic |
dopamine 2 receptor vascular endothelial growth factor A, mouse vasculotropin A animal cell adhesion conference paper disease model drug resistance female genetics hyperplasia hypophysis hypophysis tumor male mouse mouse mutant neovascularization (pathology) pathology peliosis hepatis physiology prolactinoma sexual development vascularization Animals Cell Adhesion Disease Models, Animal Drug Resistance, Neoplasm Female Hyperplasia Male Mice Mice, Knockout Neovascularization, Pathologic Peliosis Hepatis Pituitary Gland Pituitary Neoplasms Prolactinoma Receptors, Dopamine D2 Sex Characteristics Vascular Endothelial Growth Factor A |
| spellingShingle |
dopamine 2 receptor vascular endothelial growth factor A, mouse vasculotropin A animal cell adhesion conference paper disease model drug resistance female genetics hyperplasia hypophysis hypophysis tumor male mouse mouse mutant neovascularization (pathology) pathology peliosis hepatis physiology prolactinoma sexual development vascularization Animals Cell Adhesion Disease Models, Animal Drug Resistance, Neoplasm Female Hyperplasia Male Mice Mice, Knockout Neovascularization, Pathologic Peliosis Hepatis Pituitary Gland Pituitary Neoplasms Prolactinoma Receptors, Dopamine D2 Sex Characteristics Vascular Endothelial Growth Factor A Dopaminergic D2 receptor knockout mouse: An animal model of prolactinoma |
| topic_facet |
dopamine 2 receptor vascular endothelial growth factor A, mouse vasculotropin A animal cell adhesion conference paper disease model drug resistance female genetics hyperplasia hypophysis hypophysis tumor male mouse mouse mutant neovascularization (pathology) pathology peliosis hepatis physiology prolactinoma sexual development vascularization Animals Cell Adhesion Disease Models, Animal Drug Resistance, Neoplasm Female Hyperplasia Male Mice Mice, Knockout Neovascularization, Pathologic Peliosis Hepatis Pituitary Gland Pituitary Neoplasms Prolactinoma Receptors, Dopamine D2 Sex Characteristics Vascular Endothelial Growth Factor A |
| description |
Dopamine receptor type 2 (D2R) knockout mice (KO) have chronic hyperprolactinemia, pituitary hyperplasia, and a moderate decrease in MSH content. They are also growth retarded evidencing an alteration in the GH-IGF-I axis. In D2R KO, lactotropes do not show dense secretory granules but degranulated cells and fewer somatotropes, gonadotropes and thyrotropes. Prolactin levels are always higher in female than in male knockouts, and in accordance, pituitary hyperplasia is observed at 8 months only in females. After 16 months of age, highly vascularized adenomas develop, especially in females. Prominent vascular channels in the hyperplastic and adenomatous pituitaries, as well as extravasated red blood cells not contained in capillaries is also a common finding. Prolactin is not the factor that enhances the hyperplastic phenotype in females while estrogen is a permissive factor. VEGF-A expression is increased in pituitaries from D2R KO. VEGF-A is expressed in follicle stellate cells. Because D2R receptors are found in lactotropes and not in follicle stellate cells, it may be inferred that a paracrine-derived factor from lactotropes is acting on follicle stellate cells to increase VEGF-A expression. VEGF-A does not induce pituitary cell proliferation, even though it enhances prolactin secretion. But it may act on adjacent endothelial cells and participate in the angiogenic process that increases the availability of different growth factors and mitogens. The D2R knockout mouse represents a unique animal model to study dopamine-resistant prolactinomas, and VEGF-A may be an alternative therapeutic target in this pathology. Copyright © 2006 S. Karger AG. |
| title |
Dopaminergic D2 receptor knockout mouse: An animal model of prolactinoma |
| title_short |
Dopaminergic D2 receptor knockout mouse: An animal model of prolactinoma |
| title_full |
Dopaminergic D2 receptor knockout mouse: An animal model of prolactinoma |
| title_fullStr |
Dopaminergic D2 receptor knockout mouse: An animal model of prolactinoma |
| title_full_unstemmed |
Dopaminergic D2 receptor knockout mouse: An animal model of prolactinoma |
| title_sort |
dopaminergic d2 receptor knockout mouse: an animal model of prolactinoma |
| publishDate |
2006 |
| url |
https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03013073_v35_n_p50_Cristina http://hdl.handle.net/20.500.12110/paper_03013073_v35_n_p50_Cristina |
| _version_ |
1768542839564664832 |