OBJECTIVE: To evaluate for direct toxic effects of high glucose concentrations on cellular physiology in GnRH secreting immortalized GT1-1 neurons. DESIGN: Prospective experimental design. SETTING: In vitro experimental model using a cell culture system. INTERVENTION(S): GT1-1 cells were cultured in replicates in media with two different glucose concentrations (450 mg/dL and 100 mg/dL, respectively) for varying time intervals (24, 48, and 72 hours). MAIN OUTCOME MEASURE(S): Effects of glucose concentrations on GnRH secretion by the GT1-1 neurons were evaluated using a static culture model. Cell viability, cellular apoptosis, and cell cycle events in GT1-1 neurons maintained in two different glucose concentrations were assessed by flow cytometry (fluorescence-activated cell sorter) using Annexin V-PI staining. RESULT(S): Adverse influences of high glucose concentrations on GnRH secretion and cell viability were noted in cultures maintained in high glucose concentration (450 mg/dL) culture medium for varying time intervals. A significantly higher percentage of cells maintained in high glucose concentration medium demonstrated evidence of apoptosis by a fluorescence-activated cell sorter. CONCLUSION(S): We provide in vitro evidence of glucose-induced cellular toxicity in GnRH secreting GT1-1 neurons. Significant alterations in GnRH secretion, reduced cell viability, and a higher percentage of apoptotic cells were observed in GT1-1 cells maintained in high (450 mg/dL) compared with low (100 mg/dL) glucose concentration culture medium.
OBJECTIVE: To evaluate for direct toxic effects of high glucose concentrations on cellular physiology in GnRH secreting immortalized GT1-1 neurons. DESIGN: Prospective experimental design. SETTING: In vitro experimental model using a cell culture system. INTERVENTION(S): GT1-1 cells were cultured in replicates in media with two different glucose concentrations (450 mg/dL and 100 mg/dL, respectively) for varying time intervals (24, 48, and 72 hours). MAIN OUTCOME MEASURE(S): Effects of glucose concentrations on GnRH secretion by the GT1-1 neurons were evaluated using a static culture model. Cell viability, cellular apoptosis, and cell cycle events in GT1-1 neurons maintained in two different glucose concentrations were assessed by flow cytometry (fluorescence-activated cell sorter) using Annexin V-PI staining. RESULT(S): Adverse influences of high glucose concentrations on GnRH secretion and cell viability were noted in cultures maintained in high glucose concentration (450 mg/dL) culture medium for varying time intervals. A significantly higher percentage of cells maintained in high glucose concentration medium demonstrated evidence of apoptosis by a fluorescence-activated cell sorter. CONCLUSION(S): We provide in vitro evidence of glucose-induced cellular toxicity in GnRH secreting GT1-1 neurons. Significant alterations in GnRH secretion, reduced cell viability, and a higher percentage of apoptotic cells were observed in GT1-1 cells maintained in high (450 mg/dL) compared with low (100 mg/dL) glucose concentration culture medium.
Authors: Rémy Burcelin; Bernard Thorens; Micheline Glauser; Rolf C Gaillard; François P Pralong Journal: Endocrinology Date: 2003-07-03 Impact factor: 4.736
Authors: Thiago Gagliano-Jucá; Zhuoying Li; Karol M Pencina; Yusnie M Beleva; Olga D Carlson; Josephine M Egan; Shehzad Basaria Journal: Endocrine Date: 2018-09-06 Impact factor: 3.633
Authors: Pierre S Haddad; Lina Musallam; Louis C Martineau; Cory Harris; Louis Lavoie; John T Arnason; Brian Foster; Steffany Bennett; Timothy Johns; Alain Cuerrier; Emma Coon Come; Rene Coon Come; Josephine Diamond; Louise Etapp; Charlie Etapp; Jimmy George; Charlotte Husky Swallow; Johnny Husky Swallow; Mary Jolly; Andrew Kawapit; Eliza Mamianskum; John Petagumskum; Smalley Petawabano; Laurie Petawabano; Alex Weistche; Alaa Badawi Journal: Evid Based Complement Alternat Med Date: 2011-12-20 Impact factor: 2.629