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Conference Paper: Age-related changes in adrenomedullin expression and hypoxia-inducible factor 1 activity in the rat lung and their responses to hypoxia
Title | Age-related changes in adrenomedullin expression and hypoxia-inducible factor 1 activity in the rat lung and their responses to hypoxia |
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Authors | |
Issue Date | 2006 |
Publisher | Hong Kong Academy of Medicine. |
Citation | The 4th International Huaxia Congress of Endocrinology (IHCE-4), Hong Kong, 15-18 December 2006. In Hong Kong Medical Journal, 2006, v. 12 n. 6 suppl. 4, p. 69, abstract no. O52 How to Cite? |
Abstract | Objective: To investigate the effects of hypoxia on adrenomedullin (AM) gene expression during aging. Methods: Male
rats aged 3 months, 12 months and 20 months were subjected to breathing 8% of oxygen for 6 hours. AM levels in the
lung were measured by RIA while mRNA levels of preproAM, its receptor component proteins and hypoxia-inducible
factor-1a (HIF-1a) were determined by RNase protection assay and/or RT-PCR. HIF binding to DNA was measured by
electrophoretic mobility shift. Results: In the lung, there was an age-related increase in basal levels of preproAM mRNA
and AM and of the binding of hypoxia-inducible factor-1a (HIF-1a) to DNA. Upon hypoxic stimulation, HIF binding
to DNA increased in the young and middle-aged rats, but not in the old rats. AM gene expression increased in response
to hypoxia in rats of all ages but the increase was much less in the old rats. AM peptide levels in the lung decreased with
age in hypoxia. In male rats aged 3 months and 20 months subjected to hypoxia, preproAM, CRLR (calcitonin receptorlike
receptor), RAMP (receptor activity modifying proteins) mRNA and HIF-1 mRNA levels showed an increase in
basal levels but a diminished response to hypoxia in the old rats. Polysome profiling demonstrated decreases in the
percentages of translatable preproAM mRNA in response to hypoxia, with a greater decrease in the old than the young
rats. Conclusion: The age-dependent decrease in the hypoxic response of the AM system in the lung was associated
with high basal levels of HIF activity and AM expression in the old rats, but less translatable preproAM mRNA in the
old rats in response to hypoxia. Thus the HIF-AM pathway may be impaired in the aged lung and other mechanisms
may be present to maintain an AM response to hypoxia.
(This study was supported by a CRCG grant from the University of Hong Kong). |
Persistent Identifier | http://hdl.handle.net/10722/95138 |
ISSN | 2023 Impact Factor: 3.1 2023 SCImago Journal Rankings: 0.261 |
DC Field | Value | Language |
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dc.contributor.author | Hwang, ISS | en_HK |
dc.contributor.author | Fung, ML | en_HK |
dc.contributor.author | Liong, EC | en_HK |
dc.contributor.author | Tipoe, GL | en_HK |
dc.contributor.author | Tang, F | en_HK |
dc.date.accessioned | 2010-09-25T15:52:50Z | - |
dc.date.available | 2010-09-25T15:52:50Z | - |
dc.date.issued | 2006 | en_HK |
dc.identifier.citation | The 4th International Huaxia Congress of Endocrinology (IHCE-4), Hong Kong, 15-18 December 2006. In Hong Kong Medical Journal, 2006, v. 12 n. 6 suppl. 4, p. 69, abstract no. O52 | - |
dc.identifier.issn | 1024-2708 | - |
dc.identifier.uri | http://hdl.handle.net/10722/95138 | - |
dc.description.abstract | Objective: To investigate the effects of hypoxia on adrenomedullin (AM) gene expression during aging. Methods: Male rats aged 3 months, 12 months and 20 months were subjected to breathing 8% of oxygen for 6 hours. AM levels in the lung were measured by RIA while mRNA levels of preproAM, its receptor component proteins and hypoxia-inducible factor-1a (HIF-1a) were determined by RNase protection assay and/or RT-PCR. HIF binding to DNA was measured by electrophoretic mobility shift. Results: In the lung, there was an age-related increase in basal levels of preproAM mRNA and AM and of the binding of hypoxia-inducible factor-1a (HIF-1a) to DNA. Upon hypoxic stimulation, HIF binding to DNA increased in the young and middle-aged rats, but not in the old rats. AM gene expression increased in response to hypoxia in rats of all ages but the increase was much less in the old rats. AM peptide levels in the lung decreased with age in hypoxia. In male rats aged 3 months and 20 months subjected to hypoxia, preproAM, CRLR (calcitonin receptorlike receptor), RAMP (receptor activity modifying proteins) mRNA and HIF-1 mRNA levels showed an increase in basal levels but a diminished response to hypoxia in the old rats. Polysome profiling demonstrated decreases in the percentages of translatable preproAM mRNA in response to hypoxia, with a greater decrease in the old than the young rats. Conclusion: The age-dependent decrease in the hypoxic response of the AM system in the lung was associated with high basal levels of HIF activity and AM expression in the old rats, but less translatable preproAM mRNA in the old rats in response to hypoxia. Thus the HIF-AM pathway may be impaired in the aged lung and other mechanisms may be present to maintain an AM response to hypoxia. (This study was supported by a CRCG grant from the University of Hong Kong). | - |
dc.language | eng | en_HK |
dc.publisher | Hong Kong Academy of Medicine. | - |
dc.relation.ispartof | Hong Kong Medical Journal | en_HK |
dc.title | Age-related changes in adrenomedullin expression and hypoxia-inducible factor 1 activity in the rat lung and their responses to hypoxia | en_HK |
dc.type | Conference_Paper | en_HK |
dc.identifier.email | Hwang, ISS: isabelbelbel@hotmail.com | en_HK |
dc.identifier.email | Fung, ML: fungml@hkucc.hku.hk | en_HK |
dc.identifier.email | Liong, EC: eclionga@HKUCC.hku.hk | en_HK |
dc.identifier.email | Tipoe, GL: tgeorge@hkucc.hku.hk | en_HK |
dc.identifier.email | Tang, F: ftang@hkucc.hku.hk | en_HK |
dc.identifier.authority | Fung, ML=rp00433 | en_HK |
dc.identifier.authority | Tipoe, GL=rp00371 | en_HK |
dc.identifier.authority | Tang, F=rp00327 | en_HK |
dc.identifier.hkuros | 128830 | en_HK |
dc.identifier.volume | 12 | - |
dc.identifier.issue | 6 suppl. 4 | - |
dc.identifier.spage | 69, abstract no. O52 | - |
dc.identifier.epage | 69, abstract no. O52 | - |
dc.identifier.issnl | 1024-2708 | - |