Angiotensin II receptors and angiotensin II stimulation of ciliary activity in human fallopian tube

Using an antibody (6313/G2) directed against a specific sequence in the extracellular domain of the type 1 angiotensin II receptor (AT1), we demonstrated the presence of angiotensin II (AII) receptors in human fallopian tube. Immunoperoxidase staining for AT1 receptor showed positive staining in the...

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Veröffentlicht in:The journal of clinical endocrinology and metabolism 1996-07, Vol.81 (7), p.2719-2725
Hauptverfasser: SARIDOGAN, E, DJAHANBAKHCH, O, PUDDEFOOT, J. R, DEMETROULIS, C, COLLINGWOOD, K, MEHTA, J. G, VINSON, G. P
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container_end_page 2725
container_issue 7
container_start_page 2719
container_title The journal of clinical endocrinology and metabolism
container_volume 81
creator SARIDOGAN, E
DJAHANBAKHCH, O
PUDDEFOOT, J. R
DEMETROULIS, C
COLLINGWOOD, K
MEHTA, J. G
VINSON, G. P
description Using an antibody (6313/G2) directed against a specific sequence in the extracellular domain of the type 1 angiotensin II receptor (AT1), we demonstrated the presence of angiotensin II (AII) receptors in human fallopian tube. Immunoperoxidase staining for AT1 receptor showed positive staining in the epithelium of the tubal mucosa. The intensity of staining varied depending upon the hormonal status at the time of salpingectomy, being strongest in the proliferative phase of the ovarian cycle and weakest after menopause. Ligand binding assay confirmed that the AII receptor concentration was highest in the mucosa of fallopian tubes from premenopausal women. Mucosa from the ampullary segment had higher concentrations of AII receptor than the fimbrial and isthmic segments in both premenopausal and postmenopausal women. Displacement studies using specific AII receptor subtype antagonists showed that approximately 60% of the total activity could be displaced by CGP42112B (type 2 specific) and 40% by losartan (AT1 specific). Immunoblotting confirmed that the antibody detected a protein of approximately 60 kDa. Functional studies showed that AII had a stimulatory action on tubal ciliary beat frequency, but had no significant effect on myosalpingseal activity. This effect was achieved at nanomolar concentrations of AII; further increases in the AII concentration were without additional effect. The stimulatory effect of AII was inhibited by the specific AT1 antagonist losartan, whereas the type 2 antagonist, CGP42112B, had no effect. The data demonstrate that AII may play an important role in ovum transport and fertility.
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Mucosa from the ampullary segment had higher concentrations of AII receptor than the fimbrial and isthmic segments in both premenopausal and postmenopausal women. Displacement studies using specific AII receptor subtype antagonists showed that approximately 60% of the total activity could be displaced by CGP42112B (type 2 specific) and 40% by losartan (AT1 specific). Immunoblotting confirmed that the antibody detected a protein of approximately 60 kDa. Functional studies showed that AII had a stimulatory action on tubal ciliary beat frequency, but had no significant effect on myosalpingseal activity. This effect was achieved at nanomolar concentrations of AII; further increases in the AII concentration were without additional effect. The stimulatory effect of AII was inhibited by the specific AT1 antagonist losartan, whereas the type 2 antagonist, CGP42112B, had no effect. 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Psychology</subject><subject>Humans</subject><subject>Imidazoles - metabolism</subject><subject>Imidazoles - pharmacology</subject><subject>Immunoenzyme Techniques</subject><subject>Losartan</subject><subject>Mammalian female genital system</subject><subject>Morphology. Physiology</subject><subject>Oligopeptides - metabolism</subject><subject>Oligopeptides - pharmacology</subject><subject>Pregnancy</subject><subject>Premenopause</subject><subject>Receptors, Angiotensin - analysis</subject><subject>Receptors, Angiotensin - physiology</subject><subject>Tetrazoles - metabolism</subject><subject>Tetrazoles - pharmacology</subject><subject>Tissue Distribution</subject><subject>Vertebrates: reproduction</subject><issn>0021-972X</issn><issn>1945-7197</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkM1LxDAQxYMo67p68yr0IJ5szTRpkx6XxY-FBS8K3kKaJpqlTdcmFfa_N4tlwcMwj3k_HsxD6BpwBjngh63KOGQsyxlUJ2gOFS3SKNkpmmOcQ1qx_OMcXXi_xRgoLcgMzXjJihLDHKml-7R90M5bl6zXyaCV3oV-8Il0TZx_pg-2G1sZbO-S3iTKtlYO-0SqYH9s2CeR-ho76RIj27bf2ajCWOtLdBYPXl9Ne4Henx7fVi_p5vV5vVpuUkWgCCkhRGFaUyxrXknGGk4MaGOKMic1q7FilDalKSuqCsZyDnVtKBSyxJjzUjGyQHd_ubuh_x61D6KzXum2lU73oxeMA8GY5RG8_wPV0Hs_aCN2g-3iKwKwOHQqtkpwEEwcOo34zZQ71p1ujvBUYvRvJ196JVszSKesP2IESo4ZJ7-JR38V</recordid><startdate>19960701</startdate><enddate>19960701</enddate><creator>SARIDOGAN, E</creator><creator>DJAHANBAKHCH, O</creator><creator>PUDDEFOOT, J. 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P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c315t-333c04b40ab89a77d83f1eff5623b7b0c744d6f694c577281bbf415a600886c73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Angiotensin II - pharmacology</topic><topic>Angiotensin Receptor Antagonists</topic><topic>Biological and medical sciences</topic><topic>Biphenyl Compounds - metabolism</topic><topic>Biphenyl Compounds - pharmacology</topic><topic>Cilia - drug effects</topic><topic>Cilia - physiology</topic><topic>Fallopian Tubes - chemistry</topic><topic>Fallopian Tubes - ultrastructure</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Humans</topic><topic>Imidazoles - metabolism</topic><topic>Imidazoles - pharmacology</topic><topic>Immunoenzyme Techniques</topic><topic>Losartan</topic><topic>Mammalian female genital system</topic><topic>Morphology. Physiology</topic><topic>Oligopeptides - metabolism</topic><topic>Oligopeptides - pharmacology</topic><topic>Pregnancy</topic><topic>Premenopause</topic><topic>Receptors, Angiotensin - analysis</topic><topic>Receptors, Angiotensin - physiology</topic><topic>Tetrazoles - metabolism</topic><topic>Tetrazoles - pharmacology</topic><topic>Tissue Distribution</topic><topic>Vertebrates: reproduction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>SARIDOGAN, E</creatorcontrib><creatorcontrib>DJAHANBAKHCH, O</creatorcontrib><creatorcontrib>PUDDEFOOT, J. R</creatorcontrib><creatorcontrib>DEMETROULIS, C</creatorcontrib><creatorcontrib>COLLINGWOOD, K</creatorcontrib><creatorcontrib>MEHTA, J. G</creatorcontrib><creatorcontrib>VINSON, G. 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P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Angiotensin II receptors and angiotensin II stimulation of ciliary activity in human fallopian tube</atitle><jtitle>The journal of clinical endocrinology and metabolism</jtitle><addtitle>J Clin Endocrinol Metab</addtitle><date>1996-07-01</date><risdate>1996</risdate><volume>81</volume><issue>7</issue><spage>2719</spage><epage>2725</epage><pages>2719-2725</pages><issn>0021-972X</issn><eissn>1945-7197</eissn><coden>JCEMAZ</coden><abstract>Using an antibody (6313/G2) directed against a specific sequence in the extracellular domain of the type 1 angiotensin II receptor (AT1), we demonstrated the presence of angiotensin II (AII) receptors in human fallopian tube. Immunoperoxidase staining for AT1 receptor showed positive staining in the epithelium of the tubal mucosa. The intensity of staining varied depending upon the hormonal status at the time of salpingectomy, being strongest in the proliferative phase of the ovarian cycle and weakest after menopause. Ligand binding assay confirmed that the AII receptor concentration was highest in the mucosa of fallopian tubes from premenopausal women. Mucosa from the ampullary segment had higher concentrations of AII receptor than the fimbrial and isthmic segments in both premenopausal and postmenopausal women. Displacement studies using specific AII receptor subtype antagonists showed that approximately 60% of the total activity could be displaced by CGP42112B (type 2 specific) and 40% by losartan (AT1 specific). Immunoblotting confirmed that the antibody detected a protein of approximately 60 kDa. Functional studies showed that AII had a stimulatory action on tubal ciliary beat frequency, but had no significant effect on myosalpingseal activity. This effect was achieved at nanomolar concentrations of AII; further increases in the AII concentration were without additional effect. The stimulatory effect of AII was inhibited by the specific AT1 antagonist losartan, whereas the type 2 antagonist, CGP42112B, had no effect. The data demonstrate that AII may play an important role in ovum transport and fertility.</abstract><cop>Bethesda, MD</cop><pub>Endocrine Society</pub><pmid>8675601</pmid><doi>10.1210/jc.81.7.2719</doi><tpages>7</tpages></addata></record>
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subjects Angiotensin II - pharmacology
Angiotensin Receptor Antagonists
Biological and medical sciences
Biphenyl Compounds - metabolism
Biphenyl Compounds - pharmacology
Cilia - drug effects
Cilia - physiology
Fallopian Tubes - chemistry
Fallopian Tubes - ultrastructure
Female
Fundamental and applied biological sciences. Psychology
Humans
Imidazoles - metabolism
Imidazoles - pharmacology
Immunoenzyme Techniques
Losartan
Mammalian female genital system
Morphology. Physiology
Oligopeptides - metabolism
Oligopeptides - pharmacology
Pregnancy
Premenopause
Receptors, Angiotensin - analysis
Receptors, Angiotensin - physiology
Tetrazoles - metabolism
Tetrazoles - pharmacology
Tissue Distribution
Vertebrates: reproduction
title Angiotensin II receptors and angiotensin II stimulation of ciliary activity in human fallopian tube
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