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1 ic peptides by inhibiting their breakdown by neprilysin.
2 ting vascular remodeling but are degraded by neprilysin.
3 exhibited specificity for ECE-2 compared to neprilysin.
4 erting enzyme, insulin-degrading enzyme, and neprilysin.
5 lysin inhibitor, attenuated these effects of neprilysin.
6 nhibit both the renin-angiotensin system and neprilysin.
7 ta (Abeta), and the Abeta-degrading protease neprilysin.
8 substrate, and pathophysiological aspects of neprilysin.
9 arget, we used inducible drivers to modulate neprilysin 1 (Nep1) and dAbeta expression in adult DPM n
10 ched for an interaction between Amnesiac and Neprilysin 1 (Nep1), a fly neprilysin involved in memory
11 functional relationship between Amnesiac and Neprilysin 1 (Nep1), a membrane peptidase involved in me
12 data reveal a functional interaction between neprilysin 1 and amyloid peptide, suggesting that nepril
14 we show that an increase in the level of the neprilysin 1 peptidase overcomes memory deficits induced
16 Of particular interest is the NEP homolog neprilysin 2 (NEP2), which is thiorphan/phosphoramidon-s
17 tions, Abeta1-40 (20 muM) was incubated with neprilysin (300 ng/ml), an endopeptidase known to hydrol
18 opeptidase related in amino acid sequence to neprilysin, a mammalian cell-surface peptidase involved
19 is important to determine whether increased neprilysin activity also diminishes the levels of pathog
20 beta1 antagonist bisoprolol inhibited renal neprilysin activity and increased circulation NP levels
21 explore whether substances that can elevate neprilysin activity could be a rational option for treat
24 l nerves on kidney function attenuates renal neprilysin activity, augments circulating NP levels, red
27 rs individually and found that inhibition of neprilysin alone could enhance enkephalin responses to t
28 al development, was found to also target the neprilysin, aminopeptidase, and dipeptidylpeptidase clan
32 ning proved that Phe(3) is a key residue for neprilysin and aminopeptidase N (AP-N) ectoenkephalinase
33 combining NP degradation inhibition through neprilysin and angiotensin receptor blockade, has led to
34 wo of the three angiotensin-forming enzymes (neprilysin and endopeptidase 24.15) also contribute to t
38 m roles for endothelin-converting enzyme and neprilysin and indicate that reductions in these enzymes
40 t was independent of mRNA/protein changes in neprilysin and insulin-degrading enzyme and, instead, ma
41 closely similar sites as wild-type Abeta by neprilysin and insulin-degrading enzyme, the two most wi
42 dation of Abeta peptides within microglia by neprilysin and related enzymes is dramatically enhanced
43 s revealed a global myocardial response, and neprilysin and the STAT family as key regulators of intr
44 pted us to search for an interaction between neprilysins and Drosophila Abeta (dAbeta), a cleavage pr
46 three enzymes: neutral endopeptidases 24.11 (neprilysin) and 24.15 and prolyl-endopeptidase 24.26.
48 I and Ang-(1-7), together with cardiac ACE2, neprilysin, Ang II type 1 receptor (AT1), and mas recept
49 10 muM) were used to inhibit the activity of neprilysin, angiotensin-converting enzyme, or aminopepti
50 there has been no direct demonstration that neprilysin antagonizes the deposition of amyloid-beta in
53 gical target for Nep1.SIGNIFICANCE STATEMENT Neprilysins are endopeptidases known to degrade a number
55 RNA interference, we show here that all four neprilysins are involved in middle-term and long-term me
58 Finally, we provide evidence about soluble neprilysin as a biomarker surrogate in patients with hea
60 suggest that the recombinant brain-targeted neprilysin, ASN12, may be an effective treatment for AD
61 an increase in the Abeta-degrading protease neprilysin at the cell surface and a concomitant increas
62 (2, 4-dinitrophenyl) is also a substrate for neprilysin, but is hydrolyzed 10-fold more efficiently b
64 nificant regional association with BACE1 and neprilysin, but not PSD95 that regionally associated wit
65 genetically engineered form of the protease neprilysin completely arrest amyloid deposition in an ag
71 proves learning and memory deficits, whereas neprilysin deficiency aggravates the behavioral phenotyp
74 under nonpathological conditions, mammalian neprilysins degrade amyloid peptide to ensure memory for
75 er, a more widely expressed islet peptidase, neprilysin, degrades angiotensin-(1-7) into several pept
76 at the mechanism for protection conferred by neprilysin deletion involves prevention of reduced calci
77 lysin on plaques and oligomers suggests that neprilysin-dependent degradation of Abeta affects plaque
78 proach to test the alternate hypothesis that neprilysin depletion increases chronic hypoxic pulmonary
79 eficient mouse islets, angiotensin-(1-7) and neprilysin-derived degradation products angiotensin-(1-4
88 re not conserved in the other members of the neprilysin family, and based on the hypothesis that one
89 nase CD10/neutral endopeptidase 24.11 ([NEP] neprilysin) functions as part of a regulatory loop to co
94 apparent structural similarities, ECE-1 and neprilysin have been considered to differ significantly
97 CAP peptide is cleaved by the human membrane neprilysin hNEP, we searched for an interaction between
98 A screen for corresponding substrates of the neprilysin identified distinct peptides that regulate in
99 pinephrine, angiotensin II, aldosterone, and neprilysin) impair insulin sensitivity and contribute to
100 utations in MME encoding the metalloprotease neprilysin in 19 index case subjects diagnosed with axon
101 o assess the presence of circulating soluble neprilysin in a real-life cohort of HF patients and corr
104 ion of STAT1 and CASP3 and downregulation of neprilysin in both zones, suggesting r-I/R induced intri
105 Overexpression of the Abeta-degrading enzyme neprilysin in brains of human amyloid precursor protein
106 n beta-secretase activity and a reduction of neprilysin in female mice compared to males; this sugges
108 findings suggest that targeting the role of neprilysin in IAPP fibril assembly, in addition to IAPP
109 Importantly, adenoviral overexpression of neprilysin in islets cultured without FFA reproduces the
111 suggesting the sustained elevation of islet neprilysin in these mice was a compensatory mechanism ai
113 Together, our data establish a role for neprilysins in two specific memory phases and further sh
114 rading enzymes (insulin-degrading enzyme and neprilysin) in APP/CCL2 and APP mice were indistinguisha
116 romoting carcinogenesis, decreased levels of neprilysin increases inflammation and neuroendocrine cel
117 2 (angiotensin-converting enzyme 2) and NEP (neprilysin) induce the alternative, and potentially reno
125 odel, and data from the Angiotensin Receptor Neprilysin Inhibition in Heart Failure With Preserved Ej
126 We assessed the renal effects of angiotensin/neprilysin inhibition in patients who have heart failure
127 results, and further suggest the benefit of neprilysin inhibition may be partially mediated by incre
133 comparison, NT-proBNP is not a substrate of neprilysin inhibition, and thus may lead to less clinica
139 betes status, age, sex, angiotensin receptor neprilysin inhibitor (ARNI) treatment, New York Heart As
140 in receptor blocker, or angiotensin receptor-neprilysin inhibitor (ARNI) use decreased over time, and
141 receptor blocker (ARB), angiotensin receptor-neprilysin inhibitor (ARNI), beta-blocker, and mineraloc
142 CZ696, a first-in-class angiotensin receptor neprilysin inhibitor (ARNI), in patients with this disor
144 sin receptor blocker (valsartan [VAL]) and a neprilysin inhibitor (sacubitril [SAC]), was shown to be
145 tensin receptor blocker/angiotensin receptor-neprilysin inhibitor + beta-blocker + mineralocorticoid
146 combined angiotensin receptor antagonist and neprilysin inhibitor addresses 2 of the pathophysiologic
151 l size suggest that the angiotensin receptor neprilysin inhibitor LCZ696 may reduce this measure of m
152 NT) trial, in which the angiotensin receptor neprilysin inhibitor LCZ696 reduced markers of heart fai
154 re (HF) treated with an angiotensin receptor neprilysin inhibitor lived longer without being hospital
156 cardiac hypertrophy than either stand-alone neprilysin inhibitor or angiotensin receptor blocker.
157 blocker, or any dose of angiotensin receptor neprilysin inhibitor plus any dose of mineralocorticoid
158 giotensin receptor blocker valsartan and the neprilysin inhibitor prodrug sacubitril in a 1:1 ratio i
159 stigated the biological effects of ARNi with neprilysin inhibitor sacubitril and angiotensin receptor
162 in Heart Failure), the angiotensin receptor neprilysin inhibitor sacubitril/valsartan was more effec
163 d that a new angiotensin receptor antagonist-neprilysin inhibitor was superior to an angiotensin-conv
165 ospective Comparison of Angiotensin Receptor-Neprilysin Inhibitor With an Angiotensin-Converting Enzy
166 ospective Comparison of Angiotensin Receptor-Neprilysin Inhibitor With Angiotensin Converting Enzyme
167 ospective comparison of angiotensin receptor neprilysin inhibitor with angiotensin receptor blocker o
168 on treatment with ARNI (angiotensin receptor/neprilysin inhibitor) therapy or left ventricular assist
169 ive Comparison of ARNI (angiotensin-receptor-neprilysin inhibitor) with ACEI (angiotensin-converting
171 ortality when comparing angiotensin receptor-neprilysin inhibitor+BB+mineralocorticoid receptor antag
172 nhibitor or ARB+BB, and angiotensin receptor-neprilysin inhibitor+BB+mineralocorticoid receptor antag
173 tensin receptor blocker/angiotensin receptor-neprilysin inhibitor, 20% on mineralocorticoid receptor
174 tensin receptor blocker/angiotensin receptor-neprilysin inhibitor, and 50 mg of mineralocorticoid rec
175 a-blocker and one of an angiotensin receptor-neprilysin inhibitor, angiotensin-converting enzyme inhi
177 alsartan, a combination angiotensin receptor-neprilysin inhibitor, improves morbidity and mortality i
178 bines an angiotensin receptor blocker with a neprilysin inhibitor, is well tolerated, and represents
179 esized that angiotensin receptor blocker and neprilysin inhibitor, sacubitril/valsartan (Sac/Val, LCZ
180 ive Comparison of ARNI [Angiotensin Receptor-Neprilysin Inhibitor] with ACEI [Angiotensin-Converting-
181 ive Comparison of ARNI [Angiotensin Receptor-Neprilysin Inhibitor] With ACEI [Angiotensin-Converting-
182 ive Comparison of ARNI [Angiotensin Receptor-Neprilysin Inhibitor] with ACEI [Angiotensin-Converting-
183 ive Comparison of ARNI [Angiotensin Receptor-Neprilysin Inhibitor] with ARB [Angiotensin Receptor Blo
184 ive Comparison of ARNI [angiotensin receptor/neprilysin inhibitor] With ARB [angiotensin-receptor blo
185 combination of angiotensin receptor blocker/neprilysin inhibitors (ARNi)+beta-blockers (BB)+sodium-g
187 antagonists (MRA), and angiotensin receptor-neprilysin inhibitors (ARNI), have not been studied in a
189 tor antagonists [MRAs], angiotensin receptor-neprilysin inhibitors [ARNIs], and sodium/glucose cotran
190 acological therapy with angiotensin receptor-neprilysin inhibitors and device therapy deserves furthe
191 medications, especially angiotensin receptor-neprilysin inhibitors and sodium-glucose cotransporter-2
194 ceptor antagonists, and angiotensin receptor-neprilysin inhibitors were used in 85.1%, 44.4%, 28.6%,
195 nhibitors and ANG (angiotensin) II blockers, neprilysin inhibitors, and aldosterone antagonists.
196 in system inhibitors or angiotensin receptor-neprilysin inhibitors, beta blockers, mineralocorticoid
197 and weigh the clinical benefits of synthetic neprilysin inhibitors, either alone or in combination wi
198 cular pathways causing angioedema induced by neprilysin inhibitors, that is, sacubitril, are unclear,
202 's disease (AD) markers, synaptophysin, APP, neprilysin, insulin-degrading enzyme and transthyretin i
206 Together, these findings demonstrate that neprilysin is a factor associated with islet amyloid acc
213 ing live cell imaging, and that the protease neprilysin is involved in reduction of intraneuronal bet
215 tan might cause cognitive impairment because neprilysin is one of several enzymes degrading amyloid-b
217 time that with prolonged FFA exposure, islet neprilysin is upregulated and this is associated with re
219 ctivity of an Abeta-degrading endopeptidase, neprilysin, is elevated in the brains of "enriched" mice
220 elevated in endothelin-converting enzyme and neprilysin knock-out mice, and inhibitors of these enzym
221 issue, a lentiviral vector expressing human neprilysin (Lenti-Nep) was tested in transgenic mouse mo
227 l reduction of extracellular Abeta levels by neprilysin may facilitate development of HNPCs into neur
228 on and suggest that interventions to inhibit neprilysin may improve beta-cell function in obese human
229 le blood RNA expression of gene encoding for Neprilysin (MME) and miR-425 among blacks than whites.
232 t in islets, including beta-cells, and islet neprilysin mRNA and activity were found to decline with
235 t AD is with Abeta-degrading enzymes such as neprilysin (NEP) and insulin-degrading enzyme (IDE).
238 mily of Zn2+ metallopeptidases which include neprilysin (NEP) as prototype, has raised important ques
239 ression of insulin-degrading enzyme (IDE) or neprilysin (NEP) in neurons significantly reduces brain
241 an ethyl ester prodrug of LBQ657, the active neprilysin (NEP) inhibitor, and a component of LCZ696 (s
246 s evidence that the Abeta-degrading protease neprilysin (NEP) is down-regulated in normal aging and L
250 icrovessels and the Abeta-degrading protease neprilysin (NEP) occurred 14-21 d after a substantial de
251 abolism in kidney homogenates, we identified neprilysin (NEP) to be a major source of renal Ang-(1-7)
252 tein and mRNA for the Abeta-degrading enzyme neprilysin (NEP) was found, whereas various Abeta-cleari
254 Angiotensin-converting enzyme 2 (ACE-2), neprilysin (NEP), and plasma kallikrein (KLKB1) cleave a
257 by two membrane-bound Zn-metallopeptidases, neprilysin (NEP, EC 3.4.24.11) and aminopeptidase N (APN
258 levels of the metallomembrane endopeptidase neprilysin, normal levels were maintained in the exercis
261 This effect might result from degradation by neprilysin of endogenous Abeta produced and secreted by
263 re resistant to a 1-h incubation with either neprilysin or insulin degrading enzyme, whereas the mono
264 al cyclic guanosine monophosphate content by neprilysin or phosphodiesterase 9 inhibition, and myocar
265 In mouse models of Alzheimer's disease, neprilysin overexpression improves learning and memory d
267 ion of the renin-angiotensin-aldosterone and neprilysin pathways, as well as the limitations of these
268 ux and GSIS, suggesting that upregulation of neprilysin per se mediates insulin secretory dysfunction
269 s a substrate specificity similar to that of neprilysin, preferring to cleave substrates at the amino
271 hout exogenous Abeta1-40, the treatment with neprilysin reduced the number of developing colonies.
273 omprehensive multivariable analyses, soluble neprilysin remained significantly associated with both t
277 t neprilysin, but not enzymatically inactive neprilysin, resulted in a slight increase in basic fibro
283 t)Lu-DOTA-PP-F11N is less of a substrate for neprilysins than the other analogs, whereas intracellula
284 We previously characterized a recombinant neprilysin that contained a 38-amino acid brain-targetin
285 perineuronal net (PNN) and Mme encoding for Neprilysin, the enzyme degrading amyloid beta-peptides.
286 erted by esterases to LBQ657, which inhibits neprilysin, the enzyme responsible for the degradation o
288 estion, we crossed hAPP transgenic mice with neprilysin transgenic mice and analyzed their offspring.
291 ving hIAPP, analysis of hIAPP incubated with neprilysin was performed by mass spectrometry, which fai
293 ed by 54 and 75%, respectively, whereas when neprilysin was up-regulated islet amyloid deposition and
298 ding enzyme, the endogenous metallopeptidase neprilysin, which is fused to albumin to extend plasma h
299 HF patients and the positive association of neprilysin with cardiovascular mortality and morbidity f