The thyrotropin-releasing hormone-like peptides pGlu-Phe-Pro amide and pGlu-Glu-Pro amide increase plasma triiodothyronine levels in the mouse; the activity is sensitive to testosterone
Three naturally occurring peptides, pGlu-Glu-Pro amide, pGlu-Phe-Pro amide and pGlu-Gln-Pro amide, with similar structures to thyrotropin releasing hormone (TRH) have recently been identified but no studies of their in vivo activities have been reported previously. We describe here the ability of pG...
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Veröffentlicht in: | European journal of pharmacology 1998-09, Vol.358 (1), p.63-67 |
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description | Three naturally occurring peptides, pGlu-Glu-Pro amide, pGlu-Phe-Pro amide and pGlu-Gln-Pro amide, with similar structures to thyrotropin releasing hormone (TRH) have recently been identified but no studies of their in vivo activities have been reported previously. We describe here the ability of pGlu-Phe-Pro amide and pGlu-Glu-Pro amide to influence thyroid status. Subcutaneous administration of these `TRH-like' peptides in male and female CD1 mice led to increased levels of triiodothyronine (T3) and to a lesser extent tetraiodothyronine (T4) in the circulation. pGlu-Phe-Pro amide was more potent than pGlu-Glu-Pro amide; it exhibited a similar potency to pGlu-His-Pro amide (TRH). pGlu-Phe-Pro amide, pGlu-Glu-Pro amide and TRH produced significantly greater effects in the female than in the male. Castration of male mice led to increased activities, with potencies comparable to those seen in the female; in contrast treatment of female mice with testosterone resulted in reduced activities, similar to those observed in the control male. The effects of potassium deprivation on the activities of the TRH-like peptides were also investigated. This diet, which results in decreased testosterone levels in the male, led to increased activities of the TRH-like peptides and TRH, approaching the potencies observed in the female. The results demonstrate that the TRH-like peptides pGlu-Phe-Pro amide and pGlu-Glu-Pro amide which occur naturally in the thyroid gland exhibit biological activity in influencing thyroid status in vivo. The activities are sensitive to testosterone. |
doi_str_mv | 10.1016/S0014-2999(98)00593-7 |
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We describe here the ability of pGlu-Phe-Pro amide and pGlu-Glu-Pro amide to influence thyroid status. Subcutaneous administration of these `TRH-like' peptides in male and female CD1 mice led to increased levels of triiodothyronine (T3) and to a lesser extent tetraiodothyronine (T4) in the circulation. pGlu-Phe-Pro amide was more potent than pGlu-Glu-Pro amide; it exhibited a similar potency to pGlu-His-Pro amide (TRH). pGlu-Phe-Pro amide, pGlu-Glu-Pro amide and TRH produced significantly greater effects in the female than in the male. Castration of male mice led to increased activities, with potencies comparable to those seen in the female; in contrast treatment of female mice with testosterone resulted in reduced activities, similar to those observed in the control male. The effects of potassium deprivation on the activities of the TRH-like peptides were also investigated. This diet, which results in decreased testosterone levels in the male, led to increased activities of the TRH-like peptides and TRH, approaching the potencies observed in the female. The results demonstrate that the TRH-like peptides pGlu-Phe-Pro amide and pGlu-Glu-Pro amide which occur naturally in the thyroid gland exhibit biological activity in influencing thyroid status in vivo. The activities are sensitive to testosterone.</description><identifier>ISSN: 0014-2999</identifier><identifier>EISSN: 1879-0712</identifier><identifier>DOI: 10.1016/S0014-2999(98)00593-7</identifier><identifier>PMID: 9809870</identifier><identifier>CODEN: EJPHAZ</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Animals ; Antineoplastic Agents, Hormonal - pharmacology ; Biological and medical sciences ; Castration ; Female ; Fundamental and applied biological sciences. Psychology ; Hormones. Regulation ; K + deprivation ; Male ; Mice ; Oligopeptides - pharmacology ; Pyrrolidonecarboxylic Acid - analogs & derivatives ; Testosterone ; Testosterone - pharmacology ; Thyroid status ; Thyroid. Parathyroid. 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We describe here the ability of pGlu-Phe-Pro amide and pGlu-Glu-Pro amide to influence thyroid status. Subcutaneous administration of these `TRH-like' peptides in male and female CD1 mice led to increased levels of triiodothyronine (T3) and to a lesser extent tetraiodothyronine (T4) in the circulation. pGlu-Phe-Pro amide was more potent than pGlu-Glu-Pro amide; it exhibited a similar potency to pGlu-His-Pro amide (TRH). pGlu-Phe-Pro amide, pGlu-Glu-Pro amide and TRH produced significantly greater effects in the female than in the male. Castration of male mice led to increased activities, with potencies comparable to those seen in the female; in contrast treatment of female mice with testosterone resulted in reduced activities, similar to those observed in the control male. The effects of potassium deprivation on the activities of the TRH-like peptides were also investigated. This diet, which results in decreased testosterone levels in the male, led to increased activities of the TRH-like peptides and TRH, approaching the potencies observed in the female. The results demonstrate that the TRH-like peptides pGlu-Phe-Pro amide and pGlu-Glu-Pro amide which occur naturally in the thyroid gland exhibit biological activity in influencing thyroid status in vivo. The activities are sensitive to testosterone.</description><subject>Animals</subject><subject>Antineoplastic Agents, Hormonal - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Castration</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Hormones. Regulation</subject><subject>K + deprivation</subject><subject>Male</subject><subject>Mice</subject><subject>Oligopeptides - pharmacology</subject><subject>Pyrrolidonecarboxylic Acid - analogs & derivatives</subject><subject>Testosterone</subject><subject>Testosterone - pharmacology</subject><subject>Thyroid status</subject><subject>Thyroid. Parathyroid. Ultimobranchial body</subject><subject>Thyrotropin-Releasing Hormone - analogs & derivatives</subject><subject>Thyrotropin-Releasing Hormone - pharmacology</subject><subject>Thyroxine - blood</subject><subject>Thyroxine - drug effects</subject><subject>TRH (thyrotropin releasing hormone)</subject><subject>TRH-like peptide</subject><subject>Triiodothyronine - blood</subject><subject>Triiodothyronine - drug effects</subject><subject>Vertebrates: endocrinology</subject><issn>0014-2999</issn><issn>1879-0712</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkcGKFDEQhoMo67j6CAs5iOghmnSmOwkeRBZ3V1hwwfUc0km1E-1O2iQzMI_m25npGebqKZWqr6p-6kfoitH3jLLuw3dK2Zo0Sqm3Sr6jtFWciCdoxaRQhArWPEWrM_Icvcj5Fz1QTXuBLpSkSgq6Qn8fN4DLZp9iSXH2gSQYwWQffuJNTFMMQEb_G_AMc_EOMp5vxy152AB5SBGbqeawCe6YXkrntA821VG1dzR5Mrgk76OLy7LgA-ARdjDmylUBgKe4zfBxCY0tfufLHvuMM4Ts67eqjLhALjEXqAPgJXo2mDHDq9N7iX7cfHm8viP3326_Xn--J5ZLVYgYGOfWDq6XLe2abnC8tyAGroxwUvVUWGacW9dAtopxoH3TcSV709G-VwO_RG-Oc-cU_2yrAD35bGEcTYAqWQtKOVMdr2B7BG2KOScY9Jz8ZNJeM6oPlunFMn3wQyupF8u0qH1XpwXbfgJ37jp5VOuvT3WTrRmHZIL1-Yw1ay46JSv26YjVm8LOQ9LZeggWnE9gi3bR_0fIPwh9uFk</recordid><startdate>19980925</startdate><enddate>19980925</enddate><creator>Cremades, Asunción</creator><creator>Peñafiel, Rafael</creator><creator>Rausell, Victor</creator><creator>Del Rio-Garcia, Jesus</creator><creator>Smyth, Derek G.</creator><general>Elsevier B.V</general><general>Elsevier</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>19980925</creationdate><title>The thyrotropin-releasing hormone-like peptides pGlu-Phe-Pro amide and pGlu-Glu-Pro amide increase plasma triiodothyronine levels in the mouse; the activity is sensitive to testosterone</title><author>Cremades, Asunción ; Peñafiel, Rafael ; Rausell, Victor ; Del Rio-Garcia, Jesus ; Smyth, Derek G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c389t-7f133ccfdb850626fd3bce7f39a7d89b07c1add4b0785913e0b26398ba60bb9f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Animals</topic><topic>Antineoplastic Agents, Hormonal - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Castration</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Hormones. Regulation</topic><topic>K + deprivation</topic><topic>Male</topic><topic>Mice</topic><topic>Oligopeptides - pharmacology</topic><topic>Pyrrolidonecarboxylic Acid - analogs & derivatives</topic><topic>Testosterone</topic><topic>Testosterone - pharmacology</topic><topic>Thyroid status</topic><topic>Thyroid. Parathyroid. Ultimobranchial body</topic><topic>Thyrotropin-Releasing Hormone - analogs & derivatives</topic><topic>Thyrotropin-Releasing Hormone - pharmacology</topic><topic>Thyroxine - blood</topic><topic>Thyroxine - drug effects</topic><topic>TRH (thyrotropin releasing hormone)</topic><topic>TRH-like peptide</topic><topic>Triiodothyronine - blood</topic><topic>Triiodothyronine - drug effects</topic><topic>Vertebrates: endocrinology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cremades, Asunción</creatorcontrib><creatorcontrib>Peñafiel, Rafael</creatorcontrib><creatorcontrib>Rausell, Victor</creatorcontrib><creatorcontrib>Del Rio-Garcia, Jesus</creatorcontrib><creatorcontrib>Smyth, Derek G.</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>European journal of pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cremades, Asunción</au><au>Peñafiel, Rafael</au><au>Rausell, Victor</au><au>Del Rio-Garcia, Jesus</au><au>Smyth, Derek G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The thyrotropin-releasing hormone-like peptides pGlu-Phe-Pro amide and pGlu-Glu-Pro amide increase plasma triiodothyronine levels in the mouse; the activity is sensitive to testosterone</atitle><jtitle>European journal of pharmacology</jtitle><addtitle>Eur J Pharmacol</addtitle><date>1998-09-25</date><risdate>1998</risdate><volume>358</volume><issue>1</issue><spage>63</spage><epage>67</epage><pages>63-67</pages><issn>0014-2999</issn><eissn>1879-0712</eissn><coden>EJPHAZ</coden><abstract>Three naturally occurring peptides, pGlu-Glu-Pro amide, pGlu-Phe-Pro amide and pGlu-Gln-Pro amide, with similar structures to thyrotropin releasing hormone (TRH) have recently been identified but no studies of their in vivo activities have been reported previously. We describe here the ability of pGlu-Phe-Pro amide and pGlu-Glu-Pro amide to influence thyroid status. Subcutaneous administration of these `TRH-like' peptides in male and female CD1 mice led to increased levels of triiodothyronine (T3) and to a lesser extent tetraiodothyronine (T4) in the circulation. pGlu-Phe-Pro amide was more potent than pGlu-Glu-Pro amide; it exhibited a similar potency to pGlu-His-Pro amide (TRH). pGlu-Phe-Pro amide, pGlu-Glu-Pro amide and TRH produced significantly greater effects in the female than in the male. Castration of male mice led to increased activities, with potencies comparable to those seen in the female; in contrast treatment of female mice with testosterone resulted in reduced activities, similar to those observed in the control male. The effects of potassium deprivation on the activities of the TRH-like peptides were also investigated. This diet, which results in decreased testosterone levels in the male, led to increased activities of the TRH-like peptides and TRH, approaching the potencies observed in the female. The results demonstrate that the TRH-like peptides pGlu-Phe-Pro amide and pGlu-Glu-Pro amide which occur naturally in the thyroid gland exhibit biological activity in influencing thyroid status in vivo. The activities are sensitive to testosterone.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>9809870</pmid><doi>10.1016/S0014-2999(98)00593-7</doi><tpages>5</tpages></addata></record> |
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subjects | Animals Antineoplastic Agents, Hormonal - pharmacology Biological and medical sciences Castration Female Fundamental and applied biological sciences. Psychology Hormones. Regulation K + deprivation Male Mice Oligopeptides - pharmacology Pyrrolidonecarboxylic Acid - analogs & derivatives Testosterone Testosterone - pharmacology Thyroid status Thyroid. Parathyroid. Ultimobranchial body Thyrotropin-Releasing Hormone - analogs & derivatives Thyrotropin-Releasing Hormone - pharmacology Thyroxine - blood Thyroxine - drug effects TRH (thyrotropin releasing hormone) TRH-like peptide Triiodothyronine - blood Triiodothyronine - drug effects Vertebrates: endocrinology |
title | The thyrotropin-releasing hormone-like peptides pGlu-Phe-Pro amide and pGlu-Glu-Pro amide increase plasma triiodothyronine levels in the mouse; the activity is sensitive to testosterone |
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