@ARTICLE{TreeBASE2Ref20796,
author = {Yael H. Edrey and Diana Casper and Dorothee Huchon and James Mele and Jonathan A. Gelfond and Deborah M. Kristan and Eviatar Nevo and Rochelle Buffenstein},
title = {Sustained high levels of neuregulin-1 in the longest-lived rodents; a key determinant of rodent longevity.},
year = {2012},
keywords = {aging; cerebellum; erbb4; imum lifespan; max-; naked mole-rat; neuregulin-1; neurotrophic factors; spalax},
doi = {10.1111/j.1474-9726.2011.00772.x},
url = {http://dx.doi.org/10.5061/dryad.3h3f3380},
pmid = {22103690},
journal = {Aging Cell},
volume = {11},
number = {2},
pages = {213--222},
abstract = {Naked mole-rats (Heterocephalus glaber), the longest-lived rodents, live 7-10 times longer than similarly sized mice and exhibit normal activities for approximately 75% of their lives. Little is known about the mechanisms that allow them to delay the aging process and live so long. Neuregulin-1 (NRG-1) signaling is critical for normal brain function during both development and adulthood. We hypothesized that long-lived species will maintain higher levels of NRG-1 and that this contributes to their sustained brain function and concomitant maintenance of normal activity. We monitored the levels of NRG-1 and its receptor ErbB4 in H. glaber at different ages ranging from 1 day to 26 years and found that levels of NRG-1 and ErbB4 were sustained throughout development and adulthood. In addition, we compared seven rodent species with widely divergent (4-32 year) maximum lifespan potential (MLSP) and found that at a physiologically equivalent age, the longer-lived rodents had higher levels of NRG-1 and ErbB4. Moreover, phylogenetic independent contrast analyses revealed that this significant strong correlation between MLSP and NRG-1 levels was independent of phylogeny. These results suggest that NRG-1 is an important factor contributing to divergent species MLSP through its role in maintaining neuronal integrity.}
}
Citation for Study 12826

Citation title:
"Sustained high levels of neuregulin-1 in the longest-lived rodents; a key determinant of rodent longevity.".

Study name:
"Sustained high levels of neuregulin-1 in the longest-lived rodents; a key determinant of rodent longevity.".

This study is part of submission 12826
(Status: Published).
Citation
Edrey Y.H., Casper D., Huchon D., Mele J., Gelfond J.A., Kristan D.M., Nevo E., & Buffenstein R. 2012. Sustained high levels of neuregulin-1 in the longest-lived rodents; a key determinant of rodent longevity. Aging Cell, 11(2): 213-222.
Authors
-
Edrey Y.H.
-
Casper D.
-
Huchon D.
-
Mele J.
-
Gelfond J.A.
-
Kristan D.M.
-
Nevo E.
-
Buffenstein R.
Abstract
Naked mole-rats (Heterocephalus glaber), the longest-lived rodents, live 7-10 times longer than similarly sized mice and exhibit normal activities for approximately 75% of their lives. Little is known about the mechanisms that allow them to delay the aging process and live so long. Neuregulin-1 (NRG-1) signaling is critical for normal brain function during both development and adulthood. We hypothesized that long-lived species will maintain higher levels of NRG-1 and that this contributes to their sustained brain function and concomitant maintenance of normal activity. We monitored the levels of NRG-1 and its receptor ErbB4 in H. glaber at different ages ranging from 1 day to 26 years and found that levels of NRG-1 and ErbB4 were sustained throughout development and adulthood. In addition, we compared seven rodent species with widely divergent (4-32 year) maximum lifespan potential (MLSP) and found that at a physiologically equivalent age, the longer-lived rodents had higher levels of NRG-1 and ErbB4. Moreover, phylogenetic independent contrast analyses revealed that this significant strong correlation between MLSP and NRG-1 levels was independent of phylogeny. These results suggest that NRG-1 is an important factor contributing to divergent species MLSP through its role in maintaining neuronal integrity.
Keywords
aging; cerebellum; erbb4; imum lifespan; max-; naked mole-rat; neuregulin-1; neurotrophic factors; spalax
External links
About this resource
- Canonical resource URI:
http://purl.org/phylo/treebase/phylows/study/TB2:S12826
- Other versions:
Nexus
NeXML
- Show BibTeX reference
@ARTICLE{TreeBASE2Ref20796,
author = {Yael H. Edrey and Diana Casper and Dorothee Huchon and James Mele and Jonathan A. Gelfond and Deborah M. Kristan and Eviatar Nevo and Rochelle Buffenstein},
title = {Sustained high levels of neuregulin-1 in the longest-lived rodents; a key determinant of rodent longevity.},
year = {2012},
keywords = {aging; cerebellum; erbb4; imum lifespan; max-; naked mole-rat; neuregulin-1; neurotrophic factors; spalax},
doi = {10.1111/j.1474-9726.2011.00772.x},
url = {http://dx.doi.org/10.5061/dryad.3h3f3380},
pmid = {22103690},
journal = {Aging Cell},
volume = {11},
number = {2},
pages = {213--222},
abstract = {Naked mole-rats (Heterocephalus glaber), the longest-lived rodents, live 7-10 times longer than similarly sized mice and exhibit normal activities for approximately 75% of their lives. Little is known about the mechanisms that allow them to delay the aging process and live so long. Neuregulin-1 (NRG-1) signaling is critical for normal brain function during both development and adulthood. We hypothesized that long-lived species will maintain higher levels of NRG-1 and that this contributes to their sustained brain function and concomitant maintenance of normal activity. We monitored the levels of NRG-1 and its receptor ErbB4 in H. glaber at different ages ranging from 1 day to 26 years and found that levels of NRG-1 and ErbB4 were sustained throughout development and adulthood. In addition, we compared seven rodent species with widely divergent (4-32 year) maximum lifespan potential (MLSP) and found that at a physiologically equivalent age, the longer-lived rodents had higher levels of NRG-1 and ErbB4. Moreover, phylogenetic independent contrast analyses revealed that this significant strong correlation between MLSP and NRG-1 levels was independent of phylogeny. These results suggest that NRG-1 is an important factor contributing to divergent species MLSP through its role in maintaining neuronal integrity.}
}
- Show RIS reference
TY - JOUR
ID - 20796
AU - Edrey,Yael H.
AU - Casper,Diana
AU - Huchon,Dorothee
AU - Mele,James
AU - Gelfond,Jonathan A.
AU - Kristan,Deborah M.
AU - Nevo,Eviatar
AU - Buffenstein,Rochelle
T1 - Sustained high levels of neuregulin-1 in the longest-lived rodents; a key determinant of rodent longevity.
PY - 2012
KW - aging; cerebellum; erbb4; imum lifespan; max-; naked mole-rat; neuregulin-1; neurotrophic factors; spalax
UR - http://dx.doi.org/10.5061/dryad.3h3f3380
N2 - Naked mole-rats (Heterocephalus glaber), the longest-lived rodents, live 7-10 times longer than similarly sized mice and exhibit normal activities for approximately 75% of their lives. Little is known about the mechanisms that allow them to delay the aging process and live so long. Neuregulin-1 (NRG-1) signaling is critical for normal brain function during both development and adulthood. We hypothesized that long-lived species will maintain higher levels of NRG-1 and that this contributes to their sustained brain function and concomitant maintenance of normal activity. We monitored the levels of NRG-1 and its receptor ErbB4 in H. glaber at different ages ranging from 1 day to 26 years and found that levels of NRG-1 and ErbB4 were sustained throughout development and adulthood. In addition, we compared seven rodent species with widely divergent (4-32 year) maximum lifespan potential (MLSP) and found that at a physiologically equivalent age, the longer-lived rodents had higher levels of NRG-1 and ErbB4. Moreover, phylogenetic independent contrast analyses revealed that this significant strong correlation between MLSP and NRG-1 levels was independent of phylogeny. These results suggest that NRG-1 is an important factor contributing to divergent species MLSP through its role in maintaining neuronal integrity.
L3 - 10.1111/j.1474-9726.2011.00772.x
JF - Aging Cell
VL - 11
IS - 2
SP - 213
EP - 222
ER -