17A-Estradiol protects against glucosamine-induced pancreatic A-cell dysfunction

Lin Kang, Chung Hwan Chen, Meng Hsing Wu, Je Ken Chang, Fong Ming Chang, Juei Tang Cheng

Research output: Contribution to journalArticlepeer-review

15 Citations (Scopus)


Objective: Glucosamine (GlcN) is a popular supplement for osteoarthritis in postmenopausal women. Although GlcN possibly induces insulin resistance, the effects of GlcN on β-cell dysfunction are still obscure.

Methods: In the present study, we investigated changes in insulin production and A-cell apoptosis in pancreatic islets after GlcN treatment in rats with or without ovariectomy and used MIN-6 cells to investigate the protective effects and molecular mechanisms of 17β-estradiol (E2) in GlcN-induced A-cell dysfunction. The rats were divided into four groups: (1) sham operation (SHAM; n = 8); (2) SHAM with 750 mg/kg/day GlcN injected intraperitoneally for 14 days (SHAM + GlcN; n = 10); (3) ovariectomy (OVX; n = 9); and (4) OVX with 750 mg/kg/day GlcN injected intraperitoneally for 14 days (OVX + GlcN; n = 9).

Results: Both GlcN and ovariectomy reduced the expression of insulin, determined by the staining intensity of insulin and reverse polymerase chain reaction. GlcN alone also induced β-cell apoptosis, and this adverse effect was aggravated after ovariectomy. In addition, we found that GlcN decreased calcium influx and insulin secretion by decreasing the protein levels of inwardly rectifying potassium in the ATP-sensitive potassium channel. GlcN decreased the protein levels of endoplasmic reticulum (ER) stressYassociated proteins, including C/EBP homologous protein, phospho-protein kinase-like endoplasmic reticulum kinase, phospho-eukaryotic initiation factor 2α, and phospho-c-Jun N-terminal kinase. Finally, GlcN decreased cell viability. E2 counteracted GlcN-mediated attenuation in intracellular calcium concentration, extracellular insulin secretion, protein levels of inwardly rectifying potassium, cell viability, and protein levels of ER stressYassociated proteins. ICI182.780 inhibited these beneficial effects of E2.

Conclusions: GlcN impairs insulin secretion of β-cells by inhibiting Ca2+ influx and enhancing A-cell apoptosis with increases in ER stressYrelated proteins, whereas E2 counters these adverse effects of GlcN.

Original languageEnglish
Pages (from-to)1239-1248
Number of pages10
Issue number11
Publication statusPublished - 2014 Nov 10

All Science Journal Classification (ASJC) codes

  • Obstetrics and Gynaecology


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