In vivo antihypertensive mechanism of lactoferrin-derived peptides: Reversion of angiotensin I- and angiotensin II-induced hypertension in Wistar rats

Novel peptides with antihypertensive effects in SHR rats have previously been identified in lactoferrin (LF) hydrolysates. To investigate their in vivo antihypertensive mechanism, we have assessed the blood pressure lowering effects of two of these LF-derived peptides (RPYL and DPYKLRP) in Wistar rats subjected to either angiotensin I- or angiotensin II-induced hypertension. Blood pressure was measured by the tail-cuff method, hypertension was induced by subcutaneous infusion of angiotensins, and then captopril, valsartan or LF-derived peptides orally administered. Angiotensin I- and angiotensin II-induced hypertension were reversed by captopril and valsartan, respectively. RPYL and DPYKLRP reversed angiotensin I-induced hypertension, while DPYKLRP but not RPYL produced a modest reversion of angiotensin II-elicited hypertension. Neither RPYL nor DPYKLRP modified normotension. Thus, in vivo ACE inhibition is involved in the antihypertensive effects of LF-derived peptides like RPYL and DPYKLRP, while inhibition of AT1 receptor-mediated vasoconstriction plays a less relevant role.

Saved in:
Bibliographic Details
Main Authors: García Tejedor, Aurora, Castelló-Ruiz, María, Gimeno Alcañiz, José Vicente, Manzanares, Paloma, Salom, Juan B.
Other Authors: Ministerio de Educación y Ciencia (España)
Format: artículo biblioteca
Language:English
Published: Elsevier 2015-04-11
Subjects:Antihypertensive peptides, Lactoferrin-derived peptides, Angiotensin-induced hypertension, Wistar rat, In vivo ACE inhibition, Renin angiotensin system,
Online Access:http://hdl.handle.net/10261/148431
http://dx.doi.org/10.13039/501100000780
http://dx.doi.org/10.13039/501100004587
Tags: Add Tag
No Tags, Be the first to tag this record!
id dig-iata-es-10261-148431
record_format koha
spelling dig-iata-es-10261-1484312017-07-05T11:48:27Z In vivo antihypertensive mechanism of lactoferrin-derived peptides: Reversion of angiotensin I- and angiotensin II-induced hypertension in Wistar rats García Tejedor, Aurora Castelló-Ruiz, María Gimeno Alcañiz, José Vicente Manzanares, Paloma Salom, Juan B. Ministerio de Educación y Ciencia (España) European Commission Instituto de Salud Carlos III Antihypertensive peptides Lactoferrin-derived peptides Angiotensin-induced hypertension Wistar rat In vivo ACE inhibition Renin angiotensin system Novel peptides with antihypertensive effects in SHR rats have previously been identified in lactoferrin (LF) hydrolysates. To investigate their in vivo antihypertensive mechanism, we have assessed the blood pressure lowering effects of two of these LF-derived peptides (RPYL and DPYKLRP) in Wistar rats subjected to either angiotensin I- or angiotensin II-induced hypertension. Blood pressure was measured by the tail-cuff method, hypertension was induced by subcutaneous infusion of angiotensins, and then captopril, valsartan or LF-derived peptides orally administered. Angiotensin I- and angiotensin II-induced hypertension were reversed by captopril and valsartan, respectively. RPYL and DPYKLRP reversed angiotensin I-induced hypertension, while DPYKLRP but not RPYL produced a modest reversion of angiotensin II-elicited hypertension. Neither RPYL nor DPYKLRP modified normotension. Thus, in vivo ACE inhibition is involved in the antihypertensive effects of LF-derived peptides like RPYL and DPYKLRP, while inhibition of AT1 receptor-mediated vasoconstriction plays a less relevant role. This work was supported by grant AGL2010-21009 from ‘Ministerio de Educación y Ciencia – FEDER’, Consolider Ingenio 2010, Fun-C-Food, CSD2007-00063 and RETICS INVICTUS RD12/0014/0004 from ‘Instituto de Salud Carlos III’. A. García-Tejedor is recipient of a predoctoral fellowship from ‘Ministerio de Educación y Ciencia’ (BES-2011-044424). Peer reviewed 2017-04-18T10:40:39Z 2017-04-18T10:40:39Z 2015-04-11 artículo http://purl.org/coar/resource_type/c_6501 Journal of Functional Foods 15: 294-300 (2015) 1756-4646 http://hdl.handle.net/10261/148431 10.1016/j.jff.2015.03.039 http://dx.doi.org/10.13039/501100000780 http://dx.doi.org/10.13039/501100004587 en Postprint http://dx.doi.org/10.1016/j.jff.2015.03.039 Sí open Elsevier
institution IATA ES
collection DSpace
country España
countrycode ES
component Bibliográfico
access En linea
databasecode dig-iata-es
tag biblioteca
region Europa del Sur
libraryname Biblioteca del IATA España
language English
topic Antihypertensive peptides
Lactoferrin-derived peptides
Angiotensin-induced hypertension
Wistar rat
In vivo ACE inhibition
Renin angiotensin system
Antihypertensive peptides
Lactoferrin-derived peptides
Angiotensin-induced hypertension
Wistar rat
In vivo ACE inhibition
Renin angiotensin system
spellingShingle Antihypertensive peptides
Lactoferrin-derived peptides
Angiotensin-induced hypertension
Wistar rat
In vivo ACE inhibition
Renin angiotensin system
Antihypertensive peptides
Lactoferrin-derived peptides
Angiotensin-induced hypertension
Wistar rat
In vivo ACE inhibition
Renin angiotensin system
García Tejedor, Aurora
Castelló-Ruiz, María
Gimeno Alcañiz, José Vicente
Manzanares, Paloma
Salom, Juan B.
In vivo antihypertensive mechanism of lactoferrin-derived peptides: Reversion of angiotensin I- and angiotensin II-induced hypertension in Wistar rats
description Novel peptides with antihypertensive effects in SHR rats have previously been identified in lactoferrin (LF) hydrolysates. To investigate their in vivo antihypertensive mechanism, we have assessed the blood pressure lowering effects of two of these LF-derived peptides (RPYL and DPYKLRP) in Wistar rats subjected to either angiotensin I- or angiotensin II-induced hypertension. Blood pressure was measured by the tail-cuff method, hypertension was induced by subcutaneous infusion of angiotensins, and then captopril, valsartan or LF-derived peptides orally administered. Angiotensin I- and angiotensin II-induced hypertension were reversed by captopril and valsartan, respectively. RPYL and DPYKLRP reversed angiotensin I-induced hypertension, while DPYKLRP but not RPYL produced a modest reversion of angiotensin II-elicited hypertension. Neither RPYL nor DPYKLRP modified normotension. Thus, in vivo ACE inhibition is involved in the antihypertensive effects of LF-derived peptides like RPYL and DPYKLRP, while inhibition of AT1 receptor-mediated vasoconstriction plays a less relevant role.
author2 Ministerio de Educación y Ciencia (España)
author_facet Ministerio de Educación y Ciencia (España)
García Tejedor, Aurora
Castelló-Ruiz, María
Gimeno Alcañiz, José Vicente
Manzanares, Paloma
Salom, Juan B.
format artículo
topic_facet Antihypertensive peptides
Lactoferrin-derived peptides
Angiotensin-induced hypertension
Wistar rat
In vivo ACE inhibition
Renin angiotensin system
author García Tejedor, Aurora
Castelló-Ruiz, María
Gimeno Alcañiz, José Vicente
Manzanares, Paloma
Salom, Juan B.
author_sort García Tejedor, Aurora
title In vivo antihypertensive mechanism of lactoferrin-derived peptides: Reversion of angiotensin I- and angiotensin II-induced hypertension in Wistar rats
title_short In vivo antihypertensive mechanism of lactoferrin-derived peptides: Reversion of angiotensin I- and angiotensin II-induced hypertension in Wistar rats
title_full In vivo antihypertensive mechanism of lactoferrin-derived peptides: Reversion of angiotensin I- and angiotensin II-induced hypertension in Wistar rats
title_fullStr In vivo antihypertensive mechanism of lactoferrin-derived peptides: Reversion of angiotensin I- and angiotensin II-induced hypertension in Wistar rats
title_full_unstemmed In vivo antihypertensive mechanism of lactoferrin-derived peptides: Reversion of angiotensin I- and angiotensin II-induced hypertension in Wistar rats
title_sort in vivo antihypertensive mechanism of lactoferrin-derived peptides: reversion of angiotensin i- and angiotensin ii-induced hypertension in wistar rats
publisher Elsevier
publishDate 2015-04-11
url http://hdl.handle.net/10261/148431
http://dx.doi.org/10.13039/501100000780
http://dx.doi.org/10.13039/501100004587
work_keys_str_mv AT garciatejedoraurora invivoantihypertensivemechanismoflactoferrinderivedpeptidesreversionofangiotensiniandangiotensiniiinducedhypertensioninwistarrats
AT castelloruizmaria invivoantihypertensivemechanismoflactoferrinderivedpeptidesreversionofangiotensiniandangiotensiniiinducedhypertensioninwistarrats
AT gimenoalcanizjosevicente invivoantihypertensivemechanismoflactoferrinderivedpeptidesreversionofangiotensiniandangiotensiniiinducedhypertensioninwistarrats
AT manzanarespaloma invivoantihypertensivemechanismoflactoferrinderivedpeptidesreversionofangiotensiniandangiotensiniiinducedhypertensioninwistarrats
AT salomjuanb invivoantihypertensivemechanismoflactoferrinderivedpeptidesreversionofangiotensiniandangiotensiniiinducedhypertensioninwistarrats
_version_ 1777670039780982784