Cognitive impairment is associated with increased central arterial stiffness in an animal model of chronic kidney disease

Background The prevalence of cognitive impairment (CI) and dementia in end‐stage chronic kidney disease (CKD) has been estimated at 30‐60%. Cardiovascular diseases (CVD) including increased central arterial stiffness (CAS) accompany CKD development and contribute to CI. Elevated pulse wave velocity...

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Veröffentlicht in:Alzheimer's & dementia 2022-12, Vol.18 (S3), p.n/a
Hauptverfasser: Grigorova, Yulia N, Fox, Shanaya, Long, Jeffrey M, Santos, Carla Rocha Dos, McDevitt, Ross A, Zernetkina, Valentina, Haghkar, Mahdi, Wei, Wen, Morrell, Christopher H, Juhasz, Ondrej, Sodhi, Komal, Rapp, Peter R., Lakatta, Edward G, Fedorova, Olga V
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container_issue S3
container_start_page
container_title Alzheimer's & dementia
container_volume 18
creator Grigorova, Yulia N
Fox, Shanaya
Long, Jeffrey M
Santos, Carla Rocha Dos
McDevitt, Ross A
Zernetkina, Valentina
Haghkar, Mahdi
Wei, Wen
Morrell, Christopher H
Juhasz, Ondrej
Sodhi, Komal
Rapp, Peter R.
Lakatta, Edward G
Fedorova, Olga V
description Background The prevalence of cognitive impairment (CI) and dementia in end‐stage chronic kidney disease (CKD) has been estimated at 30‐60%. Cardiovascular diseases (CVD) including increased central arterial stiffness (CAS) accompany CKD development and contribute to CI. Elevated pulse wave velocity (PWV) is associated with higher mortality in CVD and CKD independently of blood pressure (BP). Marinobufagenin (MBG) is a pro‐fibrotic factor, which increases in CKD and contributes to CAS. The aim of this study was to determine whether CKD potentiates CI development via CAS and cardiovascular remodeling in a rat model of CKD. Method Four months old male Sprague‐Dawley rats were fed with 0.25% adenine (n=19; CKD group) diet to induce CKD or regular diet (n=16; CTRL group) for 8 weeks. Body weight (BW), BP, heart rate (HR), aortic PWV (aPWV), and behavioral tests were conducted at the end of the study. The level of anxiety was tested in an open field test (OFT). Morris water maze (MWM) was used to test spatial memory. Blood was collected for measurements of plasma sodium, potassium, blood urea nitrogen (BUN), hematocrit and MBG. The data were analyzed using two‐tailed unpaired t‐test and linear regression. Result Animals in the CKD group had higher levels of plasma creatinine and BUN, which indicate the development of CKD, higher plasma sodium, potassium, and MBG, and higher aPWV, lower hemoglobin, hematocrit, BW, HR, enlarged hearts, aortae, and kidneys, vs. CTRL group (Table 1). BP was similar in both groups. .Rats in CKD group spent less time in the center of open field compared to their CTRL counterparts, indicating increased anxiety‐like behavior (Figure 1 A, B). Although there was no difference in performance in MWM between the groups, there was a positive correlation between aortic weight and ability to find a hidden platform in the CKD group (Figure 1C). Conclusion We demonstrated that CKD development in young Sprague‐Dawley rats was accompanied by increased CAS, estimated as aPWV, which developed in blood pressure‐independent manner. Higher PWV was associated with a higher level of anxiety, and aortic tissue remodeling was associated with spatial memory in CKD model. Supported by NIH/NIA IRP
doi_str_mv 10.1002/alz.062506
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fullrecord <record><control><sourceid>wiley_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1002_alz_062506</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>ALZ062506</sourcerecordid><originalsourceid>FETCH-LOGICAL-c776-a387b9b24cd264b19e8bcd84fac0a4425eebcf3f19617cc02108582dd9afd3003</originalsourceid><addsrcrecordid>eNp9kE1LAzEQhoMoWKsXf0HOwtZJdrMfx1LUCgUvPXlZssnEju5HSRbL-utNafEoDMw7wzMvw8vYvYCFAJCPuv1ZQC4V5BdsJpSSiZJFdfmnc7hmNyF8AmRQCjVj02r46Gmkb-TU7TX5DvuRU-A6hMGQHtHyA407Tr3xqEMcTSS8brn2I3qKIozkXI8hRIjrY1EX191gseWD42bnh54M_yLb48QthaPRLbtyug14d-5ztn1-2q7Wyebt5XW13CSmKPJEp2XRVI3MjJV51ogKy8bYMnPagM4yqRAb41InqlwUxoAUUKpSWltpZ1OAdM4eTrbGDyF4dPXex_f8VAuoj5nVMbP6lFmExQk-UIvTP2S93Lyfb34Btsdxmw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Cognitive impairment is associated with increased central arterial stiffness in an animal model of chronic kidney disease</title><source>Wiley Online Library Journals Frontfile Complete</source><creator>Grigorova, Yulia N ; Fox, Shanaya ; Long, Jeffrey M ; Santos, Carla Rocha Dos ; McDevitt, Ross A ; Zernetkina, Valentina ; Haghkar, Mahdi ; Wei, Wen ; Morrell, Christopher H ; Juhasz, Ondrej ; Sodhi, Komal ; Rapp, Peter R. ; Lakatta, Edward G ; Fedorova, Olga V</creator><creatorcontrib>Grigorova, Yulia N ; Fox, Shanaya ; Long, Jeffrey M ; Santos, Carla Rocha Dos ; McDevitt, Ross A ; Zernetkina, Valentina ; Haghkar, Mahdi ; Wei, Wen ; Morrell, Christopher H ; Juhasz, Ondrej ; Sodhi, Komal ; Rapp, Peter R. ; Lakatta, Edward G ; Fedorova, Olga V</creatorcontrib><description>Background The prevalence of cognitive impairment (CI) and dementia in end‐stage chronic kidney disease (CKD) has been estimated at 30‐60%. Cardiovascular diseases (CVD) including increased central arterial stiffness (CAS) accompany CKD development and contribute to CI. Elevated pulse wave velocity (PWV) is associated with higher mortality in CVD and CKD independently of blood pressure (BP). Marinobufagenin (MBG) is a pro‐fibrotic factor, which increases in CKD and contributes to CAS. The aim of this study was to determine whether CKD potentiates CI development via CAS and cardiovascular remodeling in a rat model of CKD. Method Four months old male Sprague‐Dawley rats were fed with 0.25% adenine (n=19; CKD group) diet to induce CKD or regular diet (n=16; CTRL group) for 8 weeks. Body weight (BW), BP, heart rate (HR), aortic PWV (aPWV), and behavioral tests were conducted at the end of the study. The level of anxiety was tested in an open field test (OFT). Morris water maze (MWM) was used to test spatial memory. Blood was collected for measurements of plasma sodium, potassium, blood urea nitrogen (BUN), hematocrit and MBG. The data were analyzed using two‐tailed unpaired t‐test and linear regression. Result Animals in the CKD group had higher levels of plasma creatinine and BUN, which indicate the development of CKD, higher plasma sodium, potassium, and MBG, and higher aPWV, lower hemoglobin, hematocrit, BW, HR, enlarged hearts, aortae, and kidneys, vs. CTRL group (Table 1). BP was similar in both groups. .Rats in CKD group spent less time in the center of open field compared to their CTRL counterparts, indicating increased anxiety‐like behavior (Figure 1 A, B). Although there was no difference in performance in MWM between the groups, there was a positive correlation between aortic weight and ability to find a hidden platform in the CKD group (Figure 1C). Conclusion We demonstrated that CKD development in young Sprague‐Dawley rats was accompanied by increased CAS, estimated as aPWV, which developed in blood pressure‐independent manner. Higher PWV was associated with a higher level of anxiety, and aortic tissue remodeling was associated with spatial memory in CKD model. Supported by NIH/NIA IRP</description><identifier>ISSN: 1552-5260</identifier><identifier>EISSN: 1552-5279</identifier><identifier>DOI: 10.1002/alz.062506</identifier><language>eng</language><ispartof>Alzheimer's &amp; dementia, 2022-12, Vol.18 (S3), p.n/a</ispartof><rights>2022 the Alzheimer's Association.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Falz.062506$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Falz.062506$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids></links><search><creatorcontrib>Grigorova, Yulia N</creatorcontrib><creatorcontrib>Fox, Shanaya</creatorcontrib><creatorcontrib>Long, Jeffrey M</creatorcontrib><creatorcontrib>Santos, Carla Rocha Dos</creatorcontrib><creatorcontrib>McDevitt, Ross A</creatorcontrib><creatorcontrib>Zernetkina, Valentina</creatorcontrib><creatorcontrib>Haghkar, Mahdi</creatorcontrib><creatorcontrib>Wei, Wen</creatorcontrib><creatorcontrib>Morrell, Christopher H</creatorcontrib><creatorcontrib>Juhasz, Ondrej</creatorcontrib><creatorcontrib>Sodhi, Komal</creatorcontrib><creatorcontrib>Rapp, Peter R.</creatorcontrib><creatorcontrib>Lakatta, Edward G</creatorcontrib><creatorcontrib>Fedorova, Olga V</creatorcontrib><title>Cognitive impairment is associated with increased central arterial stiffness in an animal model of chronic kidney disease</title><title>Alzheimer's &amp; dementia</title><description>Background The prevalence of cognitive impairment (CI) and dementia in end‐stage chronic kidney disease (CKD) has been estimated at 30‐60%. Cardiovascular diseases (CVD) including increased central arterial stiffness (CAS) accompany CKD development and contribute to CI. Elevated pulse wave velocity (PWV) is associated with higher mortality in CVD and CKD independently of blood pressure (BP). Marinobufagenin (MBG) is a pro‐fibrotic factor, which increases in CKD and contributes to CAS. The aim of this study was to determine whether CKD potentiates CI development via CAS and cardiovascular remodeling in a rat model of CKD. Method Four months old male Sprague‐Dawley rats were fed with 0.25% adenine (n=19; CKD group) diet to induce CKD or regular diet (n=16; CTRL group) for 8 weeks. Body weight (BW), BP, heart rate (HR), aortic PWV (aPWV), and behavioral tests were conducted at the end of the study. The level of anxiety was tested in an open field test (OFT). Morris water maze (MWM) was used to test spatial memory. Blood was collected for measurements of plasma sodium, potassium, blood urea nitrogen (BUN), hematocrit and MBG. The data were analyzed using two‐tailed unpaired t‐test and linear regression. Result Animals in the CKD group had higher levels of plasma creatinine and BUN, which indicate the development of CKD, higher plasma sodium, potassium, and MBG, and higher aPWV, lower hemoglobin, hematocrit, BW, HR, enlarged hearts, aortae, and kidneys, vs. CTRL group (Table 1). BP was similar in both groups. .Rats in CKD group spent less time in the center of open field compared to their CTRL counterparts, indicating increased anxiety‐like behavior (Figure 1 A, B). Although there was no difference in performance in MWM between the groups, there was a positive correlation between aortic weight and ability to find a hidden platform in the CKD group (Figure 1C). Conclusion We demonstrated that CKD development in young Sprague‐Dawley rats was accompanied by increased CAS, estimated as aPWV, which developed in blood pressure‐independent manner. Higher PWV was associated with a higher level of anxiety, and aortic tissue remodeling was associated with spatial memory in CKD model. 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Cardiovascular diseases (CVD) including increased central arterial stiffness (CAS) accompany CKD development and contribute to CI. Elevated pulse wave velocity (PWV) is associated with higher mortality in CVD and CKD independently of blood pressure (BP). Marinobufagenin (MBG) is a pro‐fibrotic factor, which increases in CKD and contributes to CAS. The aim of this study was to determine whether CKD potentiates CI development via CAS and cardiovascular remodeling in a rat model of CKD. Method Four months old male Sprague‐Dawley rats were fed with 0.25% adenine (n=19; CKD group) diet to induce CKD or regular diet (n=16; CTRL group) for 8 weeks. Body weight (BW), BP, heart rate (HR), aortic PWV (aPWV), and behavioral tests were conducted at the end of the study. The level of anxiety was tested in an open field test (OFT). Morris water maze (MWM) was used to test spatial memory. Blood was collected for measurements of plasma sodium, potassium, blood urea nitrogen (BUN), hematocrit and MBG. The data were analyzed using two‐tailed unpaired t‐test and linear regression. Result Animals in the CKD group had higher levels of plasma creatinine and BUN, which indicate the development of CKD, higher plasma sodium, potassium, and MBG, and higher aPWV, lower hemoglobin, hematocrit, BW, HR, enlarged hearts, aortae, and kidneys, vs. CTRL group (Table 1). BP was similar in both groups. .Rats in CKD group spent less time in the center of open field compared to their CTRL counterparts, indicating increased anxiety‐like behavior (Figure 1 A, B). Although there was no difference in performance in MWM between the groups, there was a positive correlation between aortic weight and ability to find a hidden platform in the CKD group (Figure 1C). Conclusion We demonstrated that CKD development in young Sprague‐Dawley rats was accompanied by increased CAS, estimated as aPWV, which developed in blood pressure‐independent manner. Higher PWV was associated with a higher level of anxiety, and aortic tissue remodeling was associated with spatial memory in CKD model. Supported by NIH/NIA IRP</abstract><doi>10.1002/alz.062506</doi><tpages>1</tpages></addata></record>
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title Cognitive impairment is associated with increased central arterial stiffness in an animal model of chronic kidney disease
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