Reduction capacity of untreated and of repeatedly isoproterenol treated parotid gland of the mouse
Osmium impregnation was used to show possible differences of reduction capacity of perinuclear space, rough endoplasmic reticulum and the Golgi apparatus of unstimulated mouse parotid gland and in the gland after repeated pharmacological doses of isoproterenol. There were some significant difference...
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Veröffentlicht in: | Histochemistry 1989-01, Vol.92 (6), p.531-534 |
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description | Osmium impregnation was used to show possible differences of reduction capacity of perinuclear space, rough endoplasmic reticulum and the Golgi apparatus of unstimulated mouse parotid gland and in the gland after repeated pharmacological doses of isoproterenol. There were some significant differences between the staining of acinar and duct cells. In all intercalated and striated duct cells the staining is dense in the perinuclear space and in the rough endoplasmic reticulum. Osmiophility was not detected in the Golgi complex of intercalated duct cells. The staining was also lacking in the perinuclear space and endoplasmic reticulum of the acinar cells. The cis face of the Golgi complex and numerous transitional vesicles in the acinar cells showed variability of the reduction capacity of their membrane segments. In chronically treated acinar cells Os black was lacking in the Golgi cisternae, except that the numerous transitional vesicles were heavily stained. These results reveal characteristic differences of reduction capacity of endomembrane compartments in different parotid glandular cells, as well as between untreated and treated acinar cells. |
doi_str_mv | 10.1007/BF00524765 |
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There were some significant differences between the staining of acinar and duct cells. In all intercalated and striated duct cells the staining is dense in the perinuclear space and in the rough endoplasmic reticulum. Osmiophility was not detected in the Golgi complex of intercalated duct cells. The staining was also lacking in the perinuclear space and endoplasmic reticulum of the acinar cells. The cis face of the Golgi complex and numerous transitional vesicles in the acinar cells showed variability of the reduction capacity of their membrane segments. In chronically treated acinar cells Os black was lacking in the Golgi cisternae, except that the numerous transitional vesicles were heavily stained. These results reveal characteristic differences of reduction capacity of endomembrane compartments in different parotid glandular cells, as well as between untreated and treated acinar cells.</description><identifier>ISSN: 0301-5564</identifier><identifier>EISSN: 1432-119X</identifier><identifier>DOI: 10.1007/BF00524765</identifier><identifier>PMID: 2478509</identifier><identifier>CODEN: HCMYAL</identifier><language>eng</language><publisher>Berlin: Springer</publisher><subject>Animals ; Biological and medical sciences ; Female ; Fundamental and applied biological sciences. Psychology ; Isoproterenol - pharmacology ; Male ; Mice ; Microscopy, Electron - methods ; Morphology. Functional localizations ; Osmium ; Osmium Tetroxide ; Oxidation-Reduction ; Parotid Gland - drug effects ; Parotid Gland - metabolism ; Parotid Gland - ultrastructure ; Staining and Labeling ; Thyroid. Parathyroid. 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There were some significant differences between the staining of acinar and duct cells. In all intercalated and striated duct cells the staining is dense in the perinuclear space and in the rough endoplasmic reticulum. Osmiophility was not detected in the Golgi complex of intercalated duct cells. The staining was also lacking in the perinuclear space and endoplasmic reticulum of the acinar cells. The cis face of the Golgi complex and numerous transitional vesicles in the acinar cells showed variability of the reduction capacity of their membrane segments. In chronically treated acinar cells Os black was lacking in the Golgi cisternae, except that the numerous transitional vesicles were heavily stained. These results reveal characteristic differences of reduction capacity of endomembrane compartments in different parotid glandular cells, as well as between untreated and treated acinar cells.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Isoproterenol - pharmacology</subject><subject>Male</subject><subject>Mice</subject><subject>Microscopy, Electron - methods</subject><subject>Morphology. Functional localizations</subject><subject>Osmium</subject><subject>Osmium Tetroxide</subject><subject>Oxidation-Reduction</subject><subject>Parotid Gland - drug effects</subject><subject>Parotid Gland - metabolism</subject><subject>Parotid Gland - ultrastructure</subject><subject>Staining and Labeling</subject><subject>Thyroid. Parathyroid. Ultimobranchial body</subject><subject>Vertebrates: endocrinology</subject><issn>0301-5564</issn><issn>1432-119X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkM1LxDAQxYMo67p68S7kIB6Ear7bHnVxVVgQRMFbySYTrXTbmqSH_e_Nal1Pj5n5zePxEDql5IoSkl_fLgiRTORK7qEpFZxllJZv-2hKOKGZlEocoqMQPglRJM-LCZokuJCknKLVM9jBxLprsdG9NnXc4M7hoY0edASLdWu3Cw_9z9xscB263ncRPLRdg_-4XqddbfF7M37ED8DrbghwjA6cbgKcjDpDr4u7l_lDtny6f5zfLDPDKY2ZJZQRSYEzaqyVVHNmVFJROG6LQoqCl8JpZawWXAoHObiScboSGgwDwmfo4tc3pfsaIMRqXQcDTQoEKUeVl6xQtBQJvPwFje9C8OCq3tdr7TcVJdW20Oq_0ASfja7Dag12h44Npvv5eNfB6MZ53Zo67DCVc6UE4d9zJn26</recordid><startdate>19890101</startdate><enddate>19890101</enddate><creator>JEZERNIK, K</creator><creator>PIPAN, N</creator><general>Springer</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>19890101</creationdate><title>Reduction capacity of untreated and of repeatedly isoproterenol treated parotid gland of the mouse</title><author>JEZERNIK, K ; PIPAN, N</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c311t-d012051e321cdd51a32c6d5148f3d88548394fa6cda4354fe7ef9231b4aec2e03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Isoproterenol - pharmacology</topic><topic>Male</topic><topic>Mice</topic><topic>Microscopy, Electron - methods</topic><topic>Morphology. Functional localizations</topic><topic>Osmium</topic><topic>Osmium Tetroxide</topic><topic>Oxidation-Reduction</topic><topic>Parotid Gland - drug effects</topic><topic>Parotid Gland - metabolism</topic><topic>Parotid Gland - ultrastructure</topic><topic>Staining and Labeling</topic><topic>Thyroid. Parathyroid. Ultimobranchial body</topic><topic>Vertebrates: endocrinology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>JEZERNIK, K</creatorcontrib><creatorcontrib>PIPAN, N</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Histochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>JEZERNIK, K</au><au>PIPAN, N</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Reduction capacity of untreated and of repeatedly isoproterenol treated parotid gland of the mouse</atitle><jtitle>Histochemistry</jtitle><addtitle>Histochemistry</addtitle><date>1989-01-01</date><risdate>1989</risdate><volume>92</volume><issue>6</issue><spage>531</spage><epage>534</epage><pages>531-534</pages><issn>0301-5564</issn><eissn>1432-119X</eissn><coden>HCMYAL</coden><abstract>Osmium impregnation was used to show possible differences of reduction capacity of perinuclear space, rough endoplasmic reticulum and the Golgi apparatus of unstimulated mouse parotid gland and in the gland after repeated pharmacological doses of isoproterenol. There were some significant differences between the staining of acinar and duct cells. In all intercalated and striated duct cells the staining is dense in the perinuclear space and in the rough endoplasmic reticulum. Osmiophility was not detected in the Golgi complex of intercalated duct cells. The staining was also lacking in the perinuclear space and endoplasmic reticulum of the acinar cells. The cis face of the Golgi complex and numerous transitional vesicles in the acinar cells showed variability of the reduction capacity of their membrane segments. In chronically treated acinar cells Os black was lacking in the Golgi cisternae, except that the numerous transitional vesicles were heavily stained. These results reveal characteristic differences of reduction capacity of endomembrane compartments in different parotid glandular cells, as well as between untreated and treated acinar cells.</abstract><cop>Berlin</cop><pub>Springer</pub><pmid>2478509</pmid><doi>10.1007/BF00524765</doi><tpages>4</tpages></addata></record> |
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subjects | Animals Biological and medical sciences Female Fundamental and applied biological sciences. Psychology Isoproterenol - pharmacology Male Mice Microscopy, Electron - methods Morphology. Functional localizations Osmium Osmium Tetroxide Oxidation-Reduction Parotid Gland - drug effects Parotid Gland - metabolism Parotid Gland - ultrastructure Staining and Labeling Thyroid. Parathyroid. Ultimobranchial body Vertebrates: endocrinology |
title | Reduction capacity of untreated and of repeatedly isoproterenol treated parotid gland of the mouse |
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