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. Author manuscript; available in PMC: 2019 Jan 8.
Published in final edited form as: ACS Biomater Sci Eng. 2017 Dec 7;4(1):266–277. doi: 10.1021/acsbiomaterials.7b00735

Figure 5.

Figure 5

Fullerol abolishes the TNF-α-induced increase in [Ca2+]i in primary DRG neurons. (A) Representative images showing intracellular Ca2+ fluorescence of primary DRG neurons pretreated with F-12 media (control), fullerol (1 μM), TNF-α (10 ng/mL), or TNF-α (10 ng/mL) + fullerol (1 μM) overnight in the absence (upper row) or presence (lower row) of 60 mM KCl. (B) Nanofullerol neutralizes the increase in estimated intracellular Ca2+ concentration ([Ca2+]i) induced by TNF-α. Whereas neurons treated exclusively with TNF-α lead to higher [Ca2+]i, those treated with fullerol and TNF-α + fullerol show significantly lower global ([Ca2+]i). KCl-stimulated elevations in [Ca2+]i are also reduced by pretreating with fullerol. For baseline, p < 0.05, *TNF-α vs control, fullerol, and TNF-α + fullerol; #TNF-α + fullerol vs control, fullerol, and TNF-α. For KCl treated, p < 0.05, §Fullerol vs control; TNF-α vs fullerol and TNF-α + fullerol. Data are presented as mean ± SEM; 20–30 neurons were analyzed per group.