Session: 724 APS Renin-angiotensin-aldosterone system in regulation of blood pressure and renal function
(724.6) Kynurenine Infusion Disrupts Normal Blood Pressure Circadian Rhythms
Monday, April 4, 2022
10:15 AM – 12:15 PM
Location: Exhibit/Poster Hall A-B - Pennsylvania Convention Center
Poster Board Number: E179
Debra Irsik (Charlie Norwood VA Medical Center, Charlie Norwood VA Medical Center), Wendy Bollag (Charlie Norwood VA Medical Center, Charlie Norwood VA Medical Center), Carlos Isales (Augusta University)
Presenting Author Charlie Norwood VA Medical Center, Charlie Norwood VA Medical Center
Kynurenine is the first stable product of tryptophan metabolism, and its level increases with age. Elevated kynurenine/tryptophan ratios have been implicated in many aging-related diseases including chronic kidney disease (CKD). We hypothesized that chronic infusion of kynurenine would induce alterations in renal-related parameters, such as blood pressure, sodium excretion and glomerular filtration rate (GFR), that could contribute to development of age-related CKD. In an IACUC-approved study, three-month-old male Sprague Dawley rats were instrumented with aortic and venous catheters, as well as telemeters for blood pressure monitoring, and then housed in metabolic cages for urine collection. Following a five-day control period, rats received continuous kynurenine infusion (5 mg/kg, 10 mg/kg, 50 mg/kg) or vehicle for 4 weeks. We found that GFR decreased after 2 weeks of KYN treatment [1.29 (n=5) vs. 1.51 (control, n=16) or 1.50 (vehicle, n=3) mL/min p=0.04]. The normal circadian rhythm for blood pressure was disrupted by all doses of kynurenine while heart rate maintained its normal diurnal pattern. Mean arterial pressure in kynurenine-treated rats tended to increase over time compared to vehicle-treated. Kynurenine infusion also induced increased water consumption. These data suggest that kynurenine treatment impacts renal function and may contribute to the development of CKD. Non-dipping blood pressure is a significant risk factor for cardiovascular disease, even in the context of normotension. Further studies will be needed to determine the mechanism of this effect.
Career Development Award IK2BX004997 (to DLI) from the United States Veterans Affairs Biomedical Laboratory Research and Development