Low-Energy Extracorporeal Shock Wave Ameliorates Streptozotocin Induced Diabetes and Promotes Pancreatic Beta Cells Regeneration in a Rat Model.
anti-inflammatory
anti-oxidative stress
low-energy extracorporeal shock wave
pancreatic beta cells regeneration
streptozotocin induced diabetes
tissue repair
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
05 Oct 2019
05 Oct 2019
Historique:
received:
10
09
2019
revised:
02
10
2019
accepted:
03
10
2019
entrez:
9
10
2019
pubmed:
9
10
2019
medline:
11
2
2020
Statut:
epublish
Résumé
Traditional therapy for diabetes mellitus has focused on supportive treatment, and is not significant in the promotion of pancreatic beta cells regeneration. We investigated the effect of low- energy extracorporeal shock wave (SW) on a streptozotocin induced diabetes (DM) rat model. The DM rats were treated with ten sessions of low-energy SW therapy (weekly for ten consecutive weeks) or left untreated. We assessed blood glucose, hemoglobin A1c (HbA1c), urine volume, pancreatic islets area, c-peptide, glucagon-like peptide 1 (GLP-1) and insulin production, beta cells number, pancreatic tissue inflammation, oxidative stress, apoptosis, angiogenesis, and stromal cell derived factor 1 (SDF-1) ten weeks after the completion of treatment. The ten- week low-energy SW therapy regimen significantly reduced blood glucose, HbA1c, and urine volume as well as significantly enhancing pancreatic islets area, c-peptide, GLP-1, and insulin production in the rat model of DM. Moreover, low-energy SW therapy increased the beta cells number in DM rats. This was likely primarily attributed to the fact that low-energy SW therapy reduced pancreatic tissue inflammation, apoptosis, and oxidative stress as well as increasing angiogenesis, cell proliferation, and tissue repair potency. Low-energy SW therapy preserved pancreatic islets function in streptozotocin-induced DM. Low-energy SW therapy may serve as a novel noninvasive and effective treatment of DM.
Identifiants
pubmed: 31590394
pii: ijms20194934
doi: 10.3390/ijms20194934
pmc: PMC6801760
pii:
doi:
Substances chimiques
Blood Glucose
0
C-Peptide
0
Glucagon-Like Peptide 1
89750-14-1
Hemoglobin A
9034-51-9
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Kaohsiung Chang Gung Memorial Hospital
ID : CMRPD8B1401, CMRPD8B1402, CRRPD8B1403, and CMRPD8D1071
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