PP.14.07: DUAL AT1 RECEPTOR/NEPRILYSIN INHIBITION (ARNI) VS. AT1 RECEPTOR BLOCKADE IN DIABETIC TGR(MREN2)27 RATS. (June 2015)
- Record Type:
- Journal Article
- Title:
- PP.14.07: DUAL AT1 RECEPTOR/NEPRILYSIN INHIBITION (ARNI) VS. AT1 RECEPTOR BLOCKADE IN DIABETIC TGR(MREN2)27 RATS. (June 2015)
- Main Title:
- PP.14.07
- Authors:
- Roksnoer, L.
Van Veghel, R.
De Vries, R.
Garrelds, I.M.
Bhaggoe, U.M.
Friesema, E.C.H.
Leijten, F.
Hoorn, E.J.
Danser, A.H.J.
Batenburg, W.W. - Abstract:
- Abstract : Objective: The recently developed combination of an Angiotensin Receptor blocker (ARB) and a Neprilysin Inhibitor (NEPi) has beneficial effects on clinical progression and mortality of patients with heart failure as compared to enalapril. However, since NEP also degrades endothelin-1 (ET-1), ARNI may cause side effects by increasing the levels of ET-1. Indeed, we recently observed in hypertensive heterozygote TGR(mREN2)27 rats that a low but not a high (0.1 vs. 1.0 mg/kg.day) dose of the NEPi thiorphan reduced blood pressure and cardiac hypertrophy on top of the ARB irbesartan. This was due to the fact that the high dose increased ET-1, upregulated constrictor vascular ET-1 type B receptors and induced an increase in renal sodium–hydrogen exchanger 3 protein abundance. In the present study, we studied the effects of the low thiorphan dose on top of irbesartan in diabetic TGR(mREN2)27 rats. Design and method: Heterozygote TGR(mREN2)27 rats were made diabetic with streptozotocin for 5 or 12 weeks. Rats were treated in the final 3 weeks with vehicle, irbesartan (15 mg/kg.day; IRB) or IRB plus the NEPi thiorphan (0.1 mg/kg.day; ARNI). Haemodynamics were measured by telemetry in the 5 week diabetic animals. In the 12 week diabetic animals vascular reactivity was determined in isolated mesenteric arteries, renal Na+ transporters were analysed by immunoblotting, and plasma and urine were collected for biochemical analysis. Results: Baseline mean arterial blood pressureAbstract : Objective: The recently developed combination of an Angiotensin Receptor blocker (ARB) and a Neprilysin Inhibitor (NEPi) has beneficial effects on clinical progression and mortality of patients with heart failure as compared to enalapril. However, since NEP also degrades endothelin-1 (ET-1), ARNI may cause side effects by increasing the levels of ET-1. Indeed, we recently observed in hypertensive heterozygote TGR(mREN2)27 rats that a low but not a high (0.1 vs. 1.0 mg/kg.day) dose of the NEPi thiorphan reduced blood pressure and cardiac hypertrophy on top of the ARB irbesartan. This was due to the fact that the high dose increased ET-1, upregulated constrictor vascular ET-1 type B receptors and induced an increase in renal sodium–hydrogen exchanger 3 protein abundance. In the present study, we studied the effects of the low thiorphan dose on top of irbesartan in diabetic TGR(mREN2)27 rats. Design and method: Heterozygote TGR(mREN2)27 rats were made diabetic with streptozotocin for 5 or 12 weeks. Rats were treated in the final 3 weeks with vehicle, irbesartan (15 mg/kg.day; IRB) or IRB plus the NEPi thiorphan (0.1 mg/kg.day; ARNI). Haemodynamics were measured by telemetry in the 5 week diabetic animals. In the 12 week diabetic animals vascular reactivity was determined in isolated mesenteric arteries, renal Na+ transporters were analysed by immunoblotting, and plasma and urine were collected for biochemical analysis. Results: Baseline mean arterial blood pressure (MAP) was 156.8 ± 5.4 mmHg. IRB and ARNI lowered MAP identically over the 3-week period, a maximum reduction of ∼50 mmHg being reached around day 7. Heart weight/tibia length ratio was reduced after treatment with ARNI only. Proteinuria and albuminuria were observed from 8 weeks of diabetes onwards and proteinuria was significantly reduced by ARNI treatment only. Urinary volume and plasma and urinary creatinine did not change. No ET-1 rises were observed, vascular reactivity was not influenced, and the pattern of kidney sodium transporters was not affected by ARNI or IRB treatment. Conclusions: ARNI reduces cardiac hypertrophy and proteinuria in diabetic TGR(mREN2)27 rats independently of blood pressure. … (more)
- Is Part Of:
- Journal of hypertension. Volume 33(2015)Supplement 1
- Journal:
- Journal of hypertension
- Issue:
- Volume 33(2015)Supplement 1
- Issue Display:
- Volume 33, Issue 1 (2015)
- Year:
- 2015
- Volume:
- 33
- Issue:
- 1
- Issue Sort Value:
- 2015-0033-0001-0000
- Page Start:
- Page End:
- Publication Date:
- 2015-06
- Subjects:
- Hypertension -- Periodicals
Hypertension -- Periodicals
616.132005 - Journal URLs:
- http://firstsearch.oclc.org ↗
http://journals.lww.com/jhypertension/pages/default.aspx ↗
http://ovidsp.ovid.com/ovidweb.cgi?T=JS&NEWS=n&CSC=Y&PAGE=toc&D=yrovft&AN=00004872-000000000-00000 ↗
http://www.jhypertension.com/ ↗
http://journals.lww.com/pages/default.aspx ↗ - DOI:
- 10.1097/01.hjh.0000468106.00414.44 ↗
- Languages:
- English
- ISSNs:
- 1473-5598
- Deposit Type:
- Legaldeposit
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