Carbamazepine can induce kidney water absorption by increasing aquaporin 2 expression

Background. Carbamazepine (Carba) is an anticonvulsant and psychotropic drug used widely for the treatment of intellectual disability and severe pains, but the incidence of hyponatremia is a common related occurrence. This hyponatremia is frequently attributed to a SIADH induced by this drug. It is...

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Veröffentlicht in:Nephrology, dialysis, transplantation dialysis, transplantation, 2010-12, Vol.25 (12), p.3840-3845
Hauptverfasser: de Bragança, Ana C., Moyses, Zenaide P., Magaldi, Antonio J.
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creator de Bragança, Ana C.
Moyses, Zenaide P.
Magaldi, Antonio J.
description Background. Carbamazepine (Carba) is an anticonvulsant and psychotropic drug used widely for the treatment of intellectual disability and severe pains, but the incidence of hyponatremia is a common related occurrence. This hyponatremia is frequently attributed to a SIADH induced by this drug. It is also known that Carba is used to decrease the urinary volume in Diabetes Insipidus (DI) because it has an antidiuretic effect. Lithium (Li) is one of the most important drugs used to treat bipolar mood disorders. However Li has the undesirable capacity to induce DI. Nowadays, the association of these drugs is used in the treatment of patients with psychiatric and neurological problems. Methods. In vivo and in vitro (microperfusion) experiments were developed to investigate the effect of Carba in the rat Inner Medullary Collecting Duct (IMCD). Results. The results revealed that Carba was able to stimulate the V2 vasopressin receptor-Protein G complex increasing the (Pf) and water absorption. In vivo studies showed that in rats with lithium-induced DI, Carba decreased the urinary volume and increased the urinary osmolality. AQP2 expression was increased both in normal IMCD incubated with Carba and in IMCD from lithium-induced DI after Carba addition to the diet, when compared with the control. Conclusion. These results showed that the hyponatremia observed in patients using this anticonvulsant drug, at least in part, is due to the Carba capacity to increase IMCD’s Pf and that the Lithium-Carbamazepine association is beneficial to the patient.
doi_str_mv 10.1093/ndt/gfq317
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Carbamazepine (Carba) is an anticonvulsant and psychotropic drug used widely for the treatment of intellectual disability and severe pains, but the incidence of hyponatremia is a common related occurrence. This hyponatremia is frequently attributed to a SIADH induced by this drug. It is also known that Carba is used to decrease the urinary volume in Diabetes Insipidus (DI) because it has an antidiuretic effect. Lithium (Li) is one of the most important drugs used to treat bipolar mood disorders. However Li has the undesirable capacity to induce DI. Nowadays, the association of these drugs is used in the treatment of patients with psychiatric and neurological problems. Methods. In vivo and in vitro (microperfusion) experiments were developed to investigate the effect of Carba in the rat Inner Medullary Collecting Duct (IMCD). Results. The results revealed that Carba was able to stimulate the V2 vasopressin receptor-Protein G complex increasing the (Pf) and water absorption. In vivo studies showed that in rats with lithium-induced DI, Carba decreased the urinary volume and increased the urinary osmolality. AQP2 expression was increased both in normal IMCD incubated with Carba and in IMCD from lithium-induced DI after Carba addition to the diet, when compared with the control. Conclusion. These results showed that the hyponatremia observed in patients using this anticonvulsant drug, at least in part, is due to the Carba capacity to increase IMCD’s Pf and that the Lithium-Carbamazepine association is beneficial to the patient.</description><identifier>ISSN: 0931-0509</identifier><identifier>EISSN: 1460-2385</identifier><identifier>DOI: 10.1093/ndt/gfq317</identifier><identifier>PMID: 20525972</identifier><identifier>CODEN: NDTREA</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Absorption - drug effects ; Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Animals ; Anticonvulsants - adverse effects ; Anticonvulsants - pharmacology ; aquaporin 2 ; Aquaporin 2 - metabolism ; Biological and medical sciences ; carbamazepine ; Carbamazepine - adverse effects ; Carbamazepine - pharmacology ; diabetes insipidus ; Diabetes Insipidus - chemically induced ; Diabetes Insipidus - metabolism ; Disease Models, Animal ; Emergency and intensive care: renal failure. Dialysis management ; Hyponatremia - chemically induced ; Hyponatremia - metabolism ; Intensive care medicine ; Kidney Tubules, Collecting - drug effects ; Kidney Tubules, Collecting - metabolism ; lithium ; Lithium Chloride - adverse effects ; Lithium Chloride - pharmacology ; Male ; Medical sciences ; Rats ; Rats, Wistar ; Receptors, Vasopressin - metabolism ; Surgery (general aspects). Transplantations, organ and tissue grafts. 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Carbamazepine (Carba) is an anticonvulsant and psychotropic drug used widely for the treatment of intellectual disability and severe pains, but the incidence of hyponatremia is a common related occurrence. This hyponatremia is frequently attributed to a SIADH induced by this drug. It is also known that Carba is used to decrease the urinary volume in Diabetes Insipidus (DI) because it has an antidiuretic effect. Lithium (Li) is one of the most important drugs used to treat bipolar mood disorders. However Li has the undesirable capacity to induce DI. Nowadays, the association of these drugs is used in the treatment of patients with psychiatric and neurological problems. Methods. In vivo and in vitro (microperfusion) experiments were developed to investigate the effect of Carba in the rat Inner Medullary Collecting Duct (IMCD). Results. The results revealed that Carba was able to stimulate the V2 vasopressin receptor-Protein G complex increasing the (Pf) and water absorption. In vivo studies showed that in rats with lithium-induced DI, Carba decreased the urinary volume and increased the urinary osmolality. AQP2 expression was increased both in normal IMCD incubated with Carba and in IMCD from lithium-induced DI after Carba addition to the diet, when compared with the control. Conclusion. These results showed that the hyponatremia observed in patients using this anticonvulsant drug, at least in part, is due to the Carba capacity to increase IMCD’s Pf and that the Lithium-Carbamazepine association is beneficial to the patient.</description><subject>Absorption - drug effects</subject><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Animals</subject><subject>Anticonvulsants - adverse effects</subject><subject>Anticonvulsants - pharmacology</subject><subject>aquaporin 2</subject><subject>Aquaporin 2 - metabolism</subject><subject>Biological and medical sciences</subject><subject>carbamazepine</subject><subject>Carbamazepine - adverse effects</subject><subject>Carbamazepine - pharmacology</subject><subject>diabetes insipidus</subject><subject>Diabetes Insipidus - chemically induced</subject><subject>Diabetes Insipidus - metabolism</subject><subject>Disease Models, Animal</subject><subject>Emergency and intensive care: renal failure. Dialysis management</subject><subject>Hyponatremia - chemically induced</subject><subject>Hyponatremia - metabolism</subject><subject>Intensive care medicine</subject><subject>Kidney Tubules, Collecting - drug effects</subject><subject>Kidney Tubules, Collecting - metabolism</subject><subject>lithium</subject><subject>Lithium Chloride - adverse effects</subject><subject>Lithium Chloride - pharmacology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Receptors, Vasopressin - metabolism</subject><subject>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</subject><subject>Surgery of the urinary system</subject><subject>Water - metabolism</subject><subject>water absorption</subject><issn>0931-0509</issn><issn>1460-2385</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpF0F9rFDEUBfAgFrutvvgBJC8iFKbNn80keZSltkJBH6wUX8JN5k6J3c3MJjO066dvZNf6dB_OjwP3EPKes3POrLxI3XRx328l16_Igi9b1ghp1GuyqCFvmGL2mJyU8psxZoXWb8ixYEooq8WC3K4ge9jAHxxjQhog0Zi6OSB9iF3CHX2ECTMFX4Y8TnFI1O-qCBmhxHRPYTvDOOSYqKD4NGYspaK35KiHdcF3h3tKbr9c_lhdNzffrr6uPt80QVo2NVppRNP6HsPSL60BMMZCJ6wPyLkOvG-919h55dEE3SEY6FnwgivdatbKU_Jp3zvmYTtjmdwmloDrNSQc5uIMF1zWR02VZ3sZ8lBKxt6NOW4g7xxn7u-Krq7o9itW_OFQO_sNdi_032wVfDwAKAHWfYYUYvnvZKs4l7y6Zu9imfDpJYf84FottXLXd7-cvbpb_fyuuVvKZ_odjIA</recordid><startdate>20101201</startdate><enddate>20101201</enddate><creator>de Bragança, Ana C.</creator><creator>Moyses, Zenaide P.</creator><creator>Magaldi, Antonio J.</creator><general>Oxford University Press</general><scope>BSCLL</scope><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>20101201</creationdate><title>Carbamazepine can induce kidney water absorption by increasing aquaporin 2 expression</title><author>de Bragança, Ana C. ; Moyses, Zenaide P. ; Magaldi, Antonio J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c390t-757ee86bfec4b498aa889ad29bce117c1f6bb7edb5be8c7dea8af0cb215767063</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Absorption - drug effects</topic><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Animals</topic><topic>Anticonvulsants - adverse effects</topic><topic>Anticonvulsants - pharmacology</topic><topic>aquaporin 2</topic><topic>Aquaporin 2 - metabolism</topic><topic>Biological and medical sciences</topic><topic>carbamazepine</topic><topic>Carbamazepine - adverse effects</topic><topic>Carbamazepine - pharmacology</topic><topic>diabetes insipidus</topic><topic>Diabetes Insipidus - chemically induced</topic><topic>Diabetes Insipidus - metabolism</topic><topic>Disease Models, Animal</topic><topic>Emergency and intensive care: renal failure. Dialysis management</topic><topic>Hyponatremia - chemically induced</topic><topic>Hyponatremia - metabolism</topic><topic>Intensive care medicine</topic><topic>Kidney Tubules, Collecting - drug effects</topic><topic>Kidney Tubules, Collecting - metabolism</topic><topic>lithium</topic><topic>Lithium Chloride - adverse effects</topic><topic>Lithium Chloride - pharmacology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Receptors, Vasopressin - metabolism</topic><topic>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</topic><topic>Surgery of the urinary system</topic><topic>Water - metabolism</topic><topic>water absorption</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>de Bragança, Ana C.</creatorcontrib><creatorcontrib>Moyses, Zenaide P.</creatorcontrib><creatorcontrib>Magaldi, Antonio J.</creatorcontrib><collection>Istex</collection><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>Nephrology, dialysis, transplantation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>de Bragança, Ana C.</au><au>Moyses, Zenaide P.</au><au>Magaldi, Antonio J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Carbamazepine can induce kidney water absorption by increasing aquaporin 2 expression</atitle><jtitle>Nephrology, dialysis, transplantation</jtitle><addtitle>Nephrol Dial Transplant</addtitle><date>2010-12-01</date><risdate>2010</risdate><volume>25</volume><issue>12</issue><spage>3840</spage><epage>3845</epage><pages>3840-3845</pages><issn>0931-0509</issn><eissn>1460-2385</eissn><coden>NDTREA</coden><abstract>Background. Carbamazepine (Carba) is an anticonvulsant and psychotropic drug used widely for the treatment of intellectual disability and severe pains, but the incidence of hyponatremia is a common related occurrence. This hyponatremia is frequently attributed to a SIADH induced by this drug. It is also known that Carba is used to decrease the urinary volume in Diabetes Insipidus (DI) because it has an antidiuretic effect. Lithium (Li) is one of the most important drugs used to treat bipolar mood disorders. However Li has the undesirable capacity to induce DI. Nowadays, the association of these drugs is used in the treatment of patients with psychiatric and neurological problems. Methods. In vivo and in vitro (microperfusion) experiments were developed to investigate the effect of Carba in the rat Inner Medullary Collecting Duct (IMCD). Results. The results revealed that Carba was able to stimulate the V2 vasopressin receptor-Protein G complex increasing the (Pf) and water absorption. In vivo studies showed that in rats with lithium-induced DI, Carba decreased the urinary volume and increased the urinary osmolality. AQP2 expression was increased both in normal IMCD incubated with Carba and in IMCD from lithium-induced DI after Carba addition to the diet, when compared with the control. Conclusion. These results showed that the hyponatremia observed in patients using this anticonvulsant drug, at least in part, is due to the Carba capacity to increase IMCD’s Pf and that the Lithium-Carbamazepine association is beneficial to the patient.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>20525972</pmid><doi>10.1093/ndt/gfq317</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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source Oxford University Press Journals All Titles (1996-Current); MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection
subjects Absorption - drug effects
Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy
Animals
Anticonvulsants - adverse effects
Anticonvulsants - pharmacology
aquaporin 2
Aquaporin 2 - metabolism
Biological and medical sciences
carbamazepine
Carbamazepine - adverse effects
Carbamazepine - pharmacology
diabetes insipidus
Diabetes Insipidus - chemically induced
Diabetes Insipidus - metabolism
Disease Models, Animal
Emergency and intensive care: renal failure. Dialysis management
Hyponatremia - chemically induced
Hyponatremia - metabolism
Intensive care medicine
Kidney Tubules, Collecting - drug effects
Kidney Tubules, Collecting - metabolism
lithium
Lithium Chloride - adverse effects
Lithium Chloride - pharmacology
Male
Medical sciences
Rats
Rats, Wistar
Receptors, Vasopressin - metabolism
Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases
Surgery of the urinary system
Water - metabolism
water absorption
title Carbamazepine can induce kidney water absorption by increasing aquaporin 2 expression
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