Up-regulation of Hsp72 and keratin16 mediates wound healing in streptozotocin diabetic rats

BACKGROUND: Impaired wound healing is a complication of diabetes and a serious problem in clinical practice. We previously found that whey protein (WP) was able to regulate wound healing normally in streptozotocin (STZ)-dia-betic models. This subsequent study was designed to assess the effect of WP on heat shock protein-72 (Hsp72) and keratin16 (Krt16) expression during wound healing in diabetic rats. METHODS: WP at a dosage of 100 mg/kg of body weight was orally administered daily to wounded normal and STZ-diabetic rats for 8 days. RESULTS: At day 4, the WP-treated diabetic wound was significantly reduced compared to that in the corresponding control. Diabetic wounded rats developed severe inflammatory infiltration and moderate capillary dilatation and regeneration. Treated rats had mild necrotic formation, moderate infiltration, moderate to severe capillary dilatation and regeneration, in addition to moderate epidermal formation. Hsp72 and Krt16 densities showed low and dense activity in diabetic wounded and diabetic wounded treated groups, respectively. At day 8, WP-treatment of diabetic wounded animals revealed great amelioration with complete recovery and closure of the wound. Reactivity of Hsp72 and Krt16 was reversed, showing dense and low, or medium and low, activity in the diabetic wounded and diabetic wounded treated groups, respectively. Hsp72 expression in the pancreas was found to show dense reactivity with WP-treated diabetic wound rats. CONCLUSION: This data provides evidence for the potential impact of WP in the up-regulation of Hsp72 and Krt16 in T1D, resulting in an improved wound healing process in diabetic models.

Saved in:
Bibliographic Details
Main Authors: Ahmed,Rasha R., Mahmoud,Ayman, Ahmed,Osama M., Metwalli,Ali, Ebaid,Hossam
Format: Digital revista
Language:English
Published: Sociedad de Biología de Chile 2015
Online Access:http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602015000100054
Tags: Add Tag
No Tags, Be the first to tag this record!
id oai:scielo:S0716-97602015000100054
record_format ojs
spelling oai:scielo:S0716-976020150001000542016-02-16Up-regulation of Hsp72 and keratin16 mediates wound healing in streptozotocin diabetic ratsAhmed,Rasha R.Mahmoud,AymanAhmed,Osama M.Metwalli,AliEbaid,Hossam Diabetic model Whey protein Heat shock protein-72 Keratin16 Wound healing BACKGROUND: Impaired wound healing is a complication of diabetes and a serious problem in clinical practice. We previously found that whey protein (WP) was able to regulate wound healing normally in streptozotocin (STZ)-dia-betic models. This subsequent study was designed to assess the effect of WP on heat shock protein-72 (Hsp72) and keratin16 (Krt16) expression during wound healing in diabetic rats. METHODS: WP at a dosage of 100 mg/kg of body weight was orally administered daily to wounded normal and STZ-diabetic rats for 8 days. RESULTS: At day 4, the WP-treated diabetic wound was significantly reduced compared to that in the corresponding control. Diabetic wounded rats developed severe inflammatory infiltration and moderate capillary dilatation and regeneration. Treated rats had mild necrotic formation, moderate infiltration, moderate to severe capillary dilatation and regeneration, in addition to moderate epidermal formation. Hsp72 and Krt16 densities showed low and dense activity in diabetic wounded and diabetic wounded treated groups, respectively. At day 8, WP-treatment of diabetic wounded animals revealed great amelioration with complete recovery and closure of the wound. Reactivity of Hsp72 and Krt16 was reversed, showing dense and low, or medium and low, activity in the diabetic wounded and diabetic wounded treated groups, respectively. Hsp72 expression in the pancreas was found to show dense reactivity with WP-treated diabetic wound rats. CONCLUSION: This data provides evidence for the potential impact of WP in the up-regulation of Hsp72 and Krt16 in T1D, resulting in an improved wound healing process in diabetic models.info:eu-repo/semantics/openAccessSociedad de Biología de ChileBiological Research v.48 20152015-01-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602015000100054en10.1186/s40659-015-0044-5
institution SCIELO
collection OJS
country Chile
countrycode CL
component Revista
access En linea
databasecode rev-scielo-cl
tag revista
region America del Sur
libraryname SciELO
language English
format Digital
author Ahmed,Rasha R.
Mahmoud,Ayman
Ahmed,Osama M.
Metwalli,Ali
Ebaid,Hossam
spellingShingle Ahmed,Rasha R.
Mahmoud,Ayman
Ahmed,Osama M.
Metwalli,Ali
Ebaid,Hossam
Up-regulation of Hsp72 and keratin16 mediates wound healing in streptozotocin diabetic rats
author_facet Ahmed,Rasha R.
Mahmoud,Ayman
Ahmed,Osama M.
Metwalli,Ali
Ebaid,Hossam
author_sort Ahmed,Rasha R.
title Up-regulation of Hsp72 and keratin16 mediates wound healing in streptozotocin diabetic rats
title_short Up-regulation of Hsp72 and keratin16 mediates wound healing in streptozotocin diabetic rats
title_full Up-regulation of Hsp72 and keratin16 mediates wound healing in streptozotocin diabetic rats
title_fullStr Up-regulation of Hsp72 and keratin16 mediates wound healing in streptozotocin diabetic rats
title_full_unstemmed Up-regulation of Hsp72 and keratin16 mediates wound healing in streptozotocin diabetic rats
title_sort up-regulation of hsp72 and keratin16 mediates wound healing in streptozotocin diabetic rats
description BACKGROUND: Impaired wound healing is a complication of diabetes and a serious problem in clinical practice. We previously found that whey protein (WP) was able to regulate wound healing normally in streptozotocin (STZ)-dia-betic models. This subsequent study was designed to assess the effect of WP on heat shock protein-72 (Hsp72) and keratin16 (Krt16) expression during wound healing in diabetic rats. METHODS: WP at a dosage of 100 mg/kg of body weight was orally administered daily to wounded normal and STZ-diabetic rats for 8 days. RESULTS: At day 4, the WP-treated diabetic wound was significantly reduced compared to that in the corresponding control. Diabetic wounded rats developed severe inflammatory infiltration and moderate capillary dilatation and regeneration. Treated rats had mild necrotic formation, moderate infiltration, moderate to severe capillary dilatation and regeneration, in addition to moderate epidermal formation. Hsp72 and Krt16 densities showed low and dense activity in diabetic wounded and diabetic wounded treated groups, respectively. At day 8, WP-treatment of diabetic wounded animals revealed great amelioration with complete recovery and closure of the wound. Reactivity of Hsp72 and Krt16 was reversed, showing dense and low, or medium and low, activity in the diabetic wounded and diabetic wounded treated groups, respectively. Hsp72 expression in the pancreas was found to show dense reactivity with WP-treated diabetic wound rats. CONCLUSION: This data provides evidence for the potential impact of WP in the up-regulation of Hsp72 and Krt16 in T1D, resulting in an improved wound healing process in diabetic models.
publisher Sociedad de Biología de Chile
publishDate 2015
url http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602015000100054
work_keys_str_mv AT ahmedrashar upregulationofhsp72andkeratin16mediateswoundhealinginstreptozotocindiabeticrats
AT mahmoudayman upregulationofhsp72andkeratin16mediateswoundhealinginstreptozotocindiabeticrats
AT ahmedosamam upregulationofhsp72andkeratin16mediateswoundhealinginstreptozotocindiabeticrats
AT metwalliali upregulationofhsp72andkeratin16mediateswoundhealinginstreptozotocindiabeticrats
AT ebaidhossam upregulationofhsp72andkeratin16mediateswoundhealinginstreptozotocindiabeticrats
_version_ 1755990940053405696