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  • 1
    In: The FASEB Journal, Wiley, Vol. 36, No. S1 ( 2022-05)
    Type of Medium: Online Resource
    ISSN: 0892-6638 , 1530-6860
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2022
    detail.hit.zdb_id: 1468876-1
    SSG: 12
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  • 2
    In: Hypertension, Ovid Technologies (Wolters Kluwer Health), Vol. 79, No. Suppl_1 ( 2022-09)
    Abstract: BMAL1 is a core circadian clock protein that regulates most physiological functions, including blood pressure (BP). Global BMAL1 knockout (KO) male mice exhibit reduced, non-dipping BP and loss of diurnal rhythm of renal sodium (Na) excretion. Although, BP and renal Na excretion rhythm remained intact in kidney-specific BMAL1 KO male mice. The adrenal gland synthesizes hormones which influence BP rhythm and renal electrolyte handling. The role of adrenal BMAL1 in the regulation of BP and renal function remains unknown. The goal was to test the hypothesis that adrenal BMAL1 is required for normal circadian rhythms of BP and renal Na excretion. Adrenal-specific aldosterone synthase Cre positive (AS)-BMAL1 KO male mice ( n =5) and littermate Cre negative, floxed control (CNTL) male mice ( n =6) underwent a telemetry study to measure BP. Cosinor analysis was performed to assess BP rhythms. During telemetry recordings, mice were placed in metabolic cages for 5 days on a normal salt diet. The latter 3 days, 12 h urine samples were collected before each light-dark Zeitgeber (6AM and 6PM/ Zeitgeber Time (ZT)0 and ZT12) to measure night/day patterns in renal Na excretion. Kidneys were collected from a separate cohort of mice ( n =7-8/genotype) at ZT0 and ZT12 for gene expression analysis of key Na transporters. No BMAL1-dependent changes in the 24 h averages for BP were observed. Cosinor analysis revealed significant differences in BP rhythm, however. The period (time taken for a full circadian cycle, ~24 h) was significantly shortened for BP in AS-BMAL1 KO mice vs. CNTL (23 h 31 vs 24 h 16, p =0.01). Acrophase (the time at which BP peaks) was shifted ~2 hours later in KO mice (KO ZT17 h 38 vs CNTL ZT15 h 45, p =0.002). The MESOR (midline estimating statistic of rhythm) of BP remained similar between groups (KO 133.5 mmHg vs CNTL 132.7 mmHg, p =0.904). Day/night Na excretion was not different in AS-BMAL1 KO mice vs. CNTL (ANOVA interaction p =0.168). This was consistent with a lack of genotype effects on gene expression for NCC, α, β, or γ ENaC. Significant time of day effects were observed for all 4 genes (all with p 〈 0.001). In conclusion, BMAL1 KO in the adrenal gland altered BP rhythm, with no changes in renal Na excretion. This work is the first to investigate the role of adrenal BMAL1 on BP regulation.
    Type of Medium: Online Resource
    ISSN: 0194-911X , 1524-4563
    Language: English
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Publication Date: 2022
    detail.hit.zdb_id: 2094210-2
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  • 3
    In: Hypertension, Ovid Technologies (Wolters Kluwer Health), Vol. 72, No. Suppl_1 ( 2018-09)
    Abstract: Blood pressure (BP) regulation is influenced by the circadian clock as seen by its daily rhythm, with a peak occurring in the active phase and a dip during the rest phase. BMAL1 is a core circadian transcription factor which regulates the circadian clock feedback loop. BMAL1 also controls the expression of thousands of genes important for physiological functions. Others have shown that global BMAL1 knockout male mice have lower mean arterial pressure (MAP) and a loss of circadian rhythm compared to controls. Because the kidney is a critical regulator of BP, the goal of this study was to determine the BP phenotype of renal distal nephron-specific BMAL1 knockout mice (KO) vs. littermate controls (CNTL). KO were generated using Ksp-cadherin Cre. Histological analysis validated the BMAL1 KO model. MAP was measured by radiotelemetry. KO had 7 mmHg lower MAP compared to CNTL (103±2 vs. 110±0.2; P=0.03; N=4-5), however, the circadian rhythm of BP was apparent in both groups. There was no difference in activity or heart rate (P=0.7, P=0.1). Kidneys were collected at noon (midpoint of rest phase) for gene expression analysis, Table 1. HKa2 expression was increased in untreated KO vs. CNTL (1.7±0.2 vs. 1±0.1; P=0.01). We have previously linked HKa2 to renal Na handling and the mineralocorticoid response. Therefore, we assessed the BP response to a high salt diet plus mineralocorticoid treatment (HS/DOCP). MAP increased in both groups in response to HS/DOCP (P=0.03) where KO rose 6 mmHg (109±1) and WT only 2 mmHg (112±2). These results suggest that BMAL1 in the kidney plays a critical role in the regulation of BP but does not appear to contribute to the circadian rhythm of BP under the conditions tested.
    Type of Medium: Online Resource
    ISSN: 0194-911X , 1524-4563
    Language: English
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Publication Date: 2018
    detail.hit.zdb_id: 2094210-2
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  • 4
    In: Hypertension, Ovid Technologies (Wolters Kluwer Health), Vol. 76, No. Suppl_1 ( 2020-09)
    Abstract: Intro: Circadian clock factors, such as BMAL1, influence systemic blood pressure (BP) control. Previously, we generated renal distal segment BMAL1 knockout mice (KS-BMAL1 KO) that exhibit lower BP compared to control mice (CNTL) in males but not females. Additionally, male KS-BMAL1 KO retain less sodium following potassium depletion compared to CNTL, a difference not seen in females. Goal: The goal of this study was to test the hypothesis that male KS-BMAL1 KO display lower BP than CNTL in response to a potassium deficient, high salt diet. Methods: Our mouse model was generated using floxed exon 8 BMAL1 mice crossed with kidney-specific cadherin Cre+ mice to generate KS-BMAL1 KO. Floxed Cre- littermates were used as CNTL. Male mice were implanted with telemeter devices for 24-hour BP monitoring before and during administration of a low potassium diet over 7 days (0% K, 0.2% Na) and followed by a low potassium, high salt diet for 10 days (0% K, 2% Na, N=7-8). Two-way ANOVA was used to compare diet and genotype effects. Results: Following potassium depletion alone, systolic BP significantly decreased in both genotypes (P 〈 0.05). Compared to baseline, KS-BMAL KO did not exhibit the increase in BP as seen in CNT on the potassium deficient, high salt diet (CNTL: 125±2 to 132±1; KO: 123±2 to 122±2 mmHg). Neither diet nor genotype altered circadian rhythms in BP. Conclusions: BMAL1 in renal distal segments contributes to BP regulation. KS-BMAL1 KO appear to be protected from the substantial increase in BP that occurred in CNTL in response to a low potassium/high salt diet. These data suggest that BMAL1 contributes to the protection from salt-sensitive hypertension in the setting of a low potassium diet.
    Type of Medium: Online Resource
    ISSN: 0194-911X , 1524-4563
    Language: English
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Publication Date: 2020
    detail.hit.zdb_id: 2094210-2
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  • 5
    In: Clinical Science, Portland Press Ltd., Vol. 136, No. 11 ( 2022-06-17), p. 825-840
    Abstract: Acute kidney injury (AKI) due to ischemia is a serious and frequent clinical complication with mortality rates as high as 80%. Vascular congestion in the renal outer medulla occurs early after ischemia reperfusion (IR) injury, and congestion has been linked to worsened outcomes following IR. There is evidence implicating both male sex and preexisting hypertension as risk factors for poor outcomes following IR. The present study tested the hypothesis that male spontaneously hypertensive rats (SHR) have greater vascular congestion and impaired renal recovery following renal IR vs. female SHR and normotensive male Sprague-Dawley rats (SD). Thirteen-week-old male and female SHR and SD were subjected to sham surgery or 30 min of warm bilateral ischemia followed by reperfusion. Rats were euthanized 24 h or 7 days post-IR. IR increased renal injury in all groups vs. sham controls at 24 h. At 7 days post-IR, injury remained elevated only in male SHR. Histological examination of SD and SHR kidneys 24 h post-IR showed vascular congestion in males and females. Vascular congestion was sustained only in male SHR 7 days post-IR. To assess the role of vascular congestion on impaired recovery following IR, additional male and female SHR were pretreated with heparin (200 U/kg) prior to IR. Heparin pretreatment reduced IR-induced vascular congestion and improved renal function in male SHR 7 days post-IR. Interestingly, preventing increases in blood pressure (BP) in male SHR did not alter sustained vascular congestion. Our data demonstrate that IR-induced vascular congestion is a major driving factor for impaired renal recovery in male SHR.
    Type of Medium: Online Resource
    ISSN: 0143-5221 , 1470-8736
    Language: English
    Publisher: Portland Press Ltd.
    Publication Date: 2022
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  • 6
    In: Clinical Science, Portland Press Ltd., Vol. 132, No. 11 ( 2018-06-15), p. 1179-1197
    Abstract: Sodium bicarbonate (NaHCO3) slows the decline in kidney function in patients with chronic kidney disease (CKD), yet the mechanisms mediating this effect remain unclear. The Dahl salt-sensitive (SS) rat develops hypertension and progressive renal injury when fed a high salt diet; however, the effect of alkali loading on kidney injury has never been investigated in this model. We hypothesized that NaHCO3 protects from the development of renal injury in Dahl salt-sensitive rats via luminal alkalization which limits the formation of tubular casts, which are a prominent pathological feature in this model. To examine this hypothesis, we determined blood pressure and renal injury responses in Dahl SS rats drinking vehicle (0.1 M NaCl) or NaHCO3 (0.1 M) solutions as well as in Dahl SS rats lacking the voltage-gated proton channel (Hv1). We found that oral NaHCO3 reduced tubular NH4+ production, tubular cast formation, and interstitial fibrosis in rats fed a high salt diet for 2 weeks. This effect was independent of changes in blood pressure, glomerular injury, or proteinuria and did not associate with changes in renal inflammatory status. We found that null mutation of Hv1 also limited cast formation in Dahl SS rats independent of proteinuria or glomerular injury. As Hv1 is localized to the luminal membrane of TAL, our data suggest that alkalization of the luminal fluid within this segment limits cast formation in this model. Reduced cast formation, secondary to luminal alkalization within TAL segments may mediate some of the protective effects of alkali loading observed in CKD patients.
    Type of Medium: Online Resource
    ISSN: 0143-5221 , 1470-8736
    Language: English
    Publisher: Portland Press Ltd.
    Publication Date: 2018
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  • 7
    In: The FASEB Journal, Wiley, Vol. 36, No. S1 ( 2022-05)
    Type of Medium: Online Resource
    ISSN: 0892-6638 , 1530-6860
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2022
    detail.hit.zdb_id: 1468876-1
    SSG: 12
    Location Call Number Limitation Availability
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