Key result
Combination therapy with SMP-534 and lisinopril significantly decreased urinary albumin excretion, BUN, and serum creatinine, and reduced extracellular matrix accumulation in 5/6 nephrectomized rats.
Why the study?
There is a large unmet need to develop strategies for treatment of CKD, and it is unknown whether combination therapy with SMP-534 and an antihypertensive agent shows additive effects on CKD progression.
Does combination therapy with SMP-534 and lisinopril improve renal function and reduce fibrosis in a 5/6 nephrectomized rat model of CKD?
Does combination therapy with SMP-534 and lisinopril improve renal function and reduce fibrosis in a 5/6 nephrectomized rat model of CKD?
Combination therapy with the antifibrotic agent SMP-534 and the ACE inhibitor lisinopril provides additive renoprotective effects in a rat model of chronic kidney disease.
The number of patients with chronic kidney disease (CKD) has continuously grown worldwide. Treatment with antihypertensive agents reduces the rate of progression of CKD, however, there is still a large unmet need to develop strategies for the treatment of CKD. Although we have previously reported that the antifibrotic agent, SMP-534 inhibits the progression of CKD, it is unknown whether combination therapy with SMP-534 and antihypertensive agent shows additive effects on CKD. In present study, we examined whether combination therapy with SMP-534 and the antihypertensive agent, lisinopril is more effective than single therapy with SMP-534 or lisinopril on five-sixths nephrectomized (5/6Nx) rat model. Combination therapy with SMP-534 (50 mg/kg) and lisinopril (5 mg/kg) significantly decreased urinary albumin excretion, blood urea nitrogen (BUN) and serum creatinine and increased creatinine clearance in 5/6Nx rats. On the other hands, single treatment with SMP-534 or lisinopril did not improve renal function at this dose. In addition, combination therapy with SMP-534 and lisinopril significantly decreased extracellular matrix (ECM) accumulation in renal glomeruli and tubulointerstitial injury. These data suggest that combination therapy with an antifibrotic agent and an antihypertensive agent may offer a new therapeutic option for suppressing the progression of CKD.
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Tsujimura et al. (2009) studied Chronic kidney disease (n=40). SMP-534 and lisinopril vs. Vehicle, SMP-534 alone, or lisinopril alone was evaluated on Renal function (urinary albumin excretion, BUN, serum creatinine, creatinine clearance) (p=<0.01). Combination therapy with SMP-534 and lisinopril significantly decreased urinary albumin excretion, BUN, and serum creatinine, and reduced extracellular matrix accumulation in 5/6 nephrectomized rats.
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