Browsing by Subject "PPARγ agonists"

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    LOW DOSE PPARγ AGONIST INHIBITION OF CYST GROWTH IN THE PCK RAT MODEL OF POLYCYSTIC KIDNEY DISEASE
    (Office of the Vice Chancellor for Research, 2012-04-13) Flaig, Stephanie; Carr, Alexander; Gattone, Vincent; Blazer-Yost, Bonnie L.
    Polycystic kidney diseases (PKD) are genetic disorders characterized by fluid-filled cysts in kidney tubules and liver bile ducts that enlarge during the patient’s life commonly progressing to renal failure in midlife. Cyst enlarge-ment is due in part, to Cl- secretion via the cystic fibrosis transmembrane conductance regulator (CFTR) Cl- channel. Our previous studies demonstrat-ed that PPARγ agonists, insulin-sensitizing drugs used to treat diabetes, in-hibit Cl- secretion by renal collecting duct principal cells via decreased CFTR synthesis. The dose response curves for Cl- transport paralleled the EC50’s for receptor transactivation with a leftward shift, suggesting an increased sensitivity for inhibition of Cl- secretion. Our previous preclinical studies showed that high (20 mg/kg BW) dose pioglitazone, a PPARγ agonist, inhib-ited cyst growth in the PCK rat model, which is orthologous to a human form of PKD. PCK rats were fed a diet containing 3 doses of rosiglitazone (4, 0.4, and 0.04 mg/kg BW) for 24 weeks starting at weaning. 4.0 mg/kg BW rosig-litazone is analogous to 20 mg/kg BW pioglitazone used in the previous study. At the end of the study, urine, serum, kidney, liver, and heart were collected for analysis. There was a significant decrease in total kidney weight, kidney weight as a percent of body weight, and renal cyst volume in the lowest does (0.04 mg/kg BW). There was no significance difference in the other doses, and the liver and heart were not changed significantly. This showed both pioglitazone and rosiglitazone were effective in inhibiting cyst growth in the PCK rat indicating a class action of PPARγ agonists. Important-ly, the rodent data substantiated the previous tissue culture data showing that a very low dose of rosiglitazone is effective in treatment of PKD.
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    Pioglitazone Attenuates Cystic Burden in the PCK Rodent Model of Polycystic Kidney Disease
    (2010) Blazer-Yost, Bonnie; Haydon, Julie; Eggleston-Gulyas, Tracy; Chen, Jey-Hsin; Wang, Xiaofang; Gattone, Vincent; Torres, Vicente E.
    Polycystic kidney disease (PKD) is a genetic disorder characterized by growth of fluid-filled cysts predominately in kidney tubules and liver bile ducts. Currently, the clinical management of PKD is limited to cyst aspiration, surgical resection or organ transplantation. Based on an observation that PPARγ agonists such as pioglitazone and rosiglitazone decrease mRNA levels of a Cl(-) transport protein, CFTR (cystic fibrosis transmembrane conductance regulator), and the Cl(-) secretory response to vasopressin in cultured renal cells, it is hypothesized that PPARγ agonists will inhibit cyst growth. The current studies show that a 7- or 14-week pioglitazone feeding regimen inhibits renal and hepatic bile duct cyst growth in the PCK rat, a rodent model orthologous to human PKD. These studies provide proof of concept for the mechanism of action of the PPARγ agonists and suggest that this class of drugs may be effective in controlling both renal and hepatic cyst growth and fibrosis in PKD.