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Toxicol Appl Pharmacol. 2017 May 15;323:53-65. doi: 10.1016/j.taap.2017.03.014. Epub 2017 Mar 15.

The effect of angiotensin receptor neprilysin inhibitor, sacubitril/valsartan, on central nervous system amyloid-β concentrations and clearance in the cynomolgus monkey.

Author information

1
Novartis Institutes for BioMedical Research, East Hanover, NJ, USA. Electronic address: heidi.schoenfeld@novartis.com.
2
C2N Diagnostics, St. Louis, MO, USA.
3
Novartis Institutes for BioMedical Research, Cambridge, MA, USA.
4
Novartis Institutes for BioMedical Research, East Hanover, NJ, USA.
5
Charles River Laboratories ULC, Montreal, Quebec, Canada.
6
Charles River Laboratories, Inc., Reno, NV, USA.
7
Novartis Institutes for BioMedical Research, Basel, Switzerland.
8
Novartis Pharmaceuticals Corporation, East Hanover, NJ, USA.
9
Department of Neurology, Washington University School of Medicine, St. Louis, MO, USA.

Abstract

Sacubitril/valsartan (LCZ696) is the first angiotensin receptor neprilysin inhibitor approved to reduce cardiovascular mortality and hospitalization in patients with heart failure with reduced ejection fraction. As neprilysin (NEP) is one of several enzymes known to degrade amyloid-β (Aβ), there is a theoretical risk of Aβ accumulation following long-term NEP inhibition. The primary objective of this study was to evaluate the potential effects of sacubitril/valsartan on central nervous system clearance of Aβ isoforms in cynomolgus monkeys using the sensitive Stable Isotope Labeling Kinetics (SILK™)-Aβ methodology. The in vitro selectivity of valsartan, sacubitril, and its active metabolite sacubitrilat was established; sacubitrilat did not inhibit other human Aβ-degrading metalloproteases. In a 2-week study, sacubitril/valsartan (50mg/kg/day) or vehicle was orally administered to female cynomolgus monkeys in conjunction with SILK™-Aβ. Despite low cerebrospinal fluid (CSF) and brain penetration, CSF exposure to sacubitril was sufficient to inhibit NEP and resulted in an increase in the elimination half-life of Aβ1-42 (65.3%; p=0.026), Aβ1-40 (35.2%; p=0.04) and Aβtotal (29.8%; p=0.04) acutely; this returned to normal as expected with repeated dosing for 15days. CSF concentrations of newly generated Aβ (AUC(0-24h)) indicated elevations in the more aggregable form Aβ1-42 on day 1 (20.4%; p=0.039) and day 15 (34.7%; p=0.0003) and in shorter forms Aβ1-40 (23.4%; p=0.009), Aβ1-38 (64.1%; p=0.0001) and Aβtotal (50.45%; p=0.00002) on day 15. However, there were no elevations in any Aβ isoforms in the brains of these monkeys on day 16. In a second study cynomolgus monkeys were administered sacubitril/valsartan (300mg/kg) or vehicle control for 39weeks; no microscopic brain changes or Aβ deposition, as assessed by immunohistochemical staining, were present. Further clinical studies are planned to address the relevance of these findings.

KEYWORDS:

Alzheimer's disease; Amyloid beta; Angiotensin receptor neprilysin inhibitor; LCZ696; SILK-Aβ; Sacubitril/valsartan

PMID:
28315356
DOI:
10.1016/j.taap.2017.03.014
[Indexed for MEDLINE]
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