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Consequences of low-intensity light at night on cardiovascular and metabolic parameters in spontaneously hypertensive rats1
Circadian rhythms are an inherent property of physiological processes and can be disturbed by irregular environmental cycles, including artificial light at night (ALAN). Circadian disruption may contribute to many pathologies, such as hypertension, obesity, and type 2 diabetes, but the underlying me...
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Published in: | Canadian journal of physiology and pharmacology 2019, Vol.97 (9), p.863-871 |
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container_title | Canadian journal of physiology and pharmacology |
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creator | Rumanova, Valentina Sophia Okuliarova, Monika Molcan, Lubos Sutovska, Hana Zeman, Michal |
description | Circadian rhythms are an inherent property of physiological processes and can be disturbed by irregular environmental cycles, including artificial light at night (ALAN). Circadian disruption may contribute to many pathologies, such as hypertension, obesity, and type 2 diabetes, but the underlying mechanisms are not understood. Our study investigated the consequences of ALAN on cardiovascular and metabolic parameters in spontaneously hypertensive rats, which represent an animal model of essential hypertension and insulin resistance. Adult males were exposed to a 12 h light − 12 h dark cycle and the ALAN group experienced dim light at night (1–2 lx), either for 2 or 5 weeks. Rats on ALAN showed a loss of light–dark variability for systolic blood pressure, but not for heart rate. Moreover, a gradual increase of systolic blood pressure was recorded over 5 weeks of ALAN. Exposure to ALAN increased plasma insulin and hepatic triglyceride levels. An increased expression of metabolic transcription factors, Pparα and Pparγ, in the epididymal fat and a decreased expression of Glut4 in the heart was found in the ALAN group. Our results demonstrate that low-intensity ALAN can disturb blood pressure control and augment insulin resistance in spontaneously hypertensive rats, and may represent a serious risk factor for cardiometabolic diseases. |
doi_str_mv | 10.1139/cjpp-2019-0043 |
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Circadian disruption may contribute to many pathologies, such as hypertension, obesity, and type 2 diabetes, but the underlying mechanisms are not understood. Our study investigated the consequences of ALAN on cardiovascular and metabolic parameters in spontaneously hypertensive rats, which represent an animal model of essential hypertension and insulin resistance. Adult males were exposed to a 12 h light − 12 h dark cycle and the ALAN group experienced dim light at night (1–2 lx), either for 2 or 5 weeks. Rats on ALAN showed a loss of light–dark variability for systolic blood pressure, but not for heart rate. Moreover, a gradual increase of systolic blood pressure was recorded over 5 weeks of ALAN. Exposure to ALAN increased plasma insulin and hepatic triglyceride levels. An increased expression of metabolic transcription factors, Pparα and Pparγ, in the epididymal fat and a decreased expression of Glut4 in the heart was found in the ALAN group. Our results demonstrate that low-intensity ALAN can disturb blood pressure control and augment insulin resistance in spontaneously hypertensive rats, and may represent a serious risk factor for cardiometabolic diseases.</description><identifier>ISSN: 0008-4212</identifier><identifier>EISSN: 1205-7541</identifier><identifier>DOI: 10.1139/cjpp-2019-0043</identifier><language>eng</language><publisher>NRC Research Press</publisher><subject>blood pressure ; circadian ; circadien ; insulin resistance ; metabolism ; métabolisme ; PPAR ; récepteurs activés par les proliférateurs de peroxysomes ; résistance à l’insuline ; tension artérielle</subject><ispartof>Canadian journal of physiology and pharmacology, 2019, Vol.97 (9), p.863-871</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids></links><search><creatorcontrib>Rumanova, Valentina Sophia</creatorcontrib><creatorcontrib>Okuliarova, Monika</creatorcontrib><creatorcontrib>Molcan, Lubos</creatorcontrib><creatorcontrib>Sutovska, Hana</creatorcontrib><creatorcontrib>Zeman, Michal</creatorcontrib><title>Consequences of low-intensity light at night on cardiovascular and metabolic parameters in spontaneously hypertensive rats1</title><title>Canadian journal of physiology and pharmacology</title><description>Circadian rhythms are an inherent property of physiological processes and can be disturbed by irregular environmental cycles, including artificial light at night (ALAN). Circadian disruption may contribute to many pathologies, such as hypertension, obesity, and type 2 diabetes, but the underlying mechanisms are not understood. Our study investigated the consequences of ALAN on cardiovascular and metabolic parameters in spontaneously hypertensive rats, which represent an animal model of essential hypertension and insulin resistance. Adult males were exposed to a 12 h light − 12 h dark cycle and the ALAN group experienced dim light at night (1–2 lx), either for 2 or 5 weeks. Rats on ALAN showed a loss of light–dark variability for systolic blood pressure, but not for heart rate. Moreover, a gradual increase of systolic blood pressure was recorded over 5 weeks of ALAN. Exposure to ALAN increased plasma insulin and hepatic triglyceride levels. An increased expression of metabolic transcription factors, Pparα and Pparγ, in the epididymal fat and a decreased expression of Glut4 in the heart was found in the ALAN group. Our results demonstrate that low-intensity ALAN can disturb blood pressure control and augment insulin resistance in spontaneously hypertensive rats, and may represent a serious risk factor for cardiometabolic diseases.</description><subject>blood pressure</subject><subject>circadian</subject><subject>circadien</subject><subject>insulin resistance</subject><subject>metabolism</subject><subject>métabolisme</subject><subject>PPAR</subject><subject>récepteurs activés par les proliférateurs de peroxysomes</subject><subject>résistance à l’insuline</subject><subject>tension artérielle</subject><issn>0008-4212</issn><issn>1205-7541</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNqdj01OwzAQhS0EEuVny3ouYLCTFNJ1BeIA7K2pOyWuXNvMOEURl6epOAGr977Fe9Kn1IM1j9a2qye_L0U3xq60MV17oRa2MUv9suzspVoYY3rdNba5Vjci-xM-922_UD_rnIS-RkqeBPIOYv7WIVVKEuoEMXwOFbBCOpecwCNvQz6i-DEiA6YtHKjiJsfgoSDjiYgFQgIpOVVMlEeJEwxTIT7_HgkYq9g7dbXDKHT_l7fKvr1-rN91Ys8khOwHVzgckCdnjZst3WzpZks3W7b_2fwCMF9gKA</recordid><startdate>2019</startdate><enddate>2019</enddate><creator>Rumanova, Valentina Sophia</creator><creator>Okuliarova, Monika</creator><creator>Molcan, Lubos</creator><creator>Sutovska, Hana</creator><creator>Zeman, Michal</creator><general>NRC Research Press</general><scope/></search><sort><creationdate>2019</creationdate><title>Consequences of low-intensity light at night on cardiovascular and metabolic parameters in spontaneously hypertensive rats1</title><author>Rumanova, Valentina Sophia ; Okuliarova, Monika ; Molcan, Lubos ; Sutovska, Hana ; Zeman, Michal</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-nrcresearch_primary_10_1139_cjpp_2019_00433</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>blood pressure</topic><topic>circadian</topic><topic>circadien</topic><topic>insulin resistance</topic><topic>metabolism</topic><topic>métabolisme</topic><topic>PPAR</topic><topic>récepteurs activés par les proliférateurs de peroxysomes</topic><topic>résistance à l’insuline</topic><topic>tension artérielle</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rumanova, Valentina Sophia</creatorcontrib><creatorcontrib>Okuliarova, Monika</creatorcontrib><creatorcontrib>Molcan, Lubos</creatorcontrib><creatorcontrib>Sutovska, Hana</creatorcontrib><creatorcontrib>Zeman, Michal</creatorcontrib><jtitle>Canadian journal of physiology and pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rumanova, Valentina Sophia</au><au>Okuliarova, Monika</au><au>Molcan, Lubos</au><au>Sutovska, Hana</au><au>Zeman, Michal</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Consequences of low-intensity light at night on cardiovascular and metabolic parameters in spontaneously hypertensive rats1</atitle><jtitle>Canadian journal of physiology and pharmacology</jtitle><date>2019</date><risdate>2019</risdate><volume>97</volume><issue>9</issue><spage>863</spage><epage>871</epage><pages>863-871</pages><issn>0008-4212</issn><eissn>1205-7541</eissn><abstract>Circadian rhythms are an inherent property of physiological processes and can be disturbed by irregular environmental cycles, including artificial light at night (ALAN). Circadian disruption may contribute to many pathologies, such as hypertension, obesity, and type 2 diabetes, but the underlying mechanisms are not understood. Our study investigated the consequences of ALAN on cardiovascular and metabolic parameters in spontaneously hypertensive rats, which represent an animal model of essential hypertension and insulin resistance. Adult males were exposed to a 12 h light − 12 h dark cycle and the ALAN group experienced dim light at night (1–2 lx), either for 2 or 5 weeks. Rats on ALAN showed a loss of light–dark variability for systolic blood pressure, but not for heart rate. Moreover, a gradual increase of systolic blood pressure was recorded over 5 weeks of ALAN. Exposure to ALAN increased plasma insulin and hepatic triglyceride levels. An increased expression of metabolic transcription factors, Pparα and Pparγ, in the epididymal fat and a decreased expression of Glut4 in the heart was found in the ALAN group. Our results demonstrate that low-intensity ALAN can disturb blood pressure control and augment insulin resistance in spontaneously hypertensive rats, and may represent a serious risk factor for cardiometabolic diseases.</abstract><pub>NRC Research Press</pub><doi>10.1139/cjpp-2019-0043</doi></addata></record> |
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subjects | blood pressure circadian circadien insulin resistance metabolism métabolisme PPAR récepteurs activés par les proliférateurs de peroxysomes résistance à l’insuline tension artérielle |
title | Consequences of low-intensity light at night on cardiovascular and metabolic parameters in spontaneously hypertensive rats1 |
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