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. Author manuscript; available in PMC: 2009 Apr 22.
Published in final edited form as: Neuroscience. 2008 Feb 19;153(1):279–288. doi: 10.1016/j.neuroscience.2008.02.006

Table 1.

Resting [Ca2+]i (nM) levels among subpopulations of DRG neurons from naïve and inflamed rats

Subpop. Stats DiI+ Stats DiI−
Naïve (n) CFA (n) Naïve (n) CFA (n)
Small S < 0.01
C > 0.05
I < 0.01
138 ± 8 (20) 144 ± 8 (19) S > 0.05
C < 0.05
I > 0.05
122 ± 4 (72) 138 ± 6 (72)
Medium 114 ± 6 (25) 145 ± 6 (42) 120 ± 5 (38) 135 ± 7 (33)
Large 121 ± 8 (18) 102 ± 8 (12) 118 ± 4 (39) 125 ± 5 (31)
IB4+ S < 0.01
C > 0.05
I < 0.01
125 ± 5 (33) 150 ± 5 (48) S > 0.05
C < 0.01
I > 0.05
120 ± 3 (81) 140 ± 6 (72)
IB4− 123 ± 7 (30) 114 ± 6 (25) 120 ± 4 (68) 128 ± 4 (64)
CAP+ S > 0.05
C > 0.05
I > 0.05
128 ± 5 (36) 141 ± 5 (56) S > 0.05
C < 0.05
I > 0.05
121 ± 3 (74) 139 ± 5 (80)
CAP− 118 ± 7 (27) 126 ± 10 (17) 120 ± 3 (75) 128 ± 5 (56)

Small, Medium and Large are cell body diameter. IB4 is isolectin B4. CAP is capsaicin. Data are mean ± SEM. The number in parentheses is the number of neurons studied in each group. Two-way ANOVA was used to assess the presence of main effects associated with subpopulation (S: cell body diameter, IB4 binding or CAP sensitivity) and inflammation (C: Naïve versus CFA) as well as a significant interaction (I) between the two. DiI+ and DiI− neurons were analyzed separately. Results of this analysis are indicated in columns labeled Stats. Post-hoc analysis (Holm-Sidak test) indicated that resting [Ca2+]i was significantly (p < 0.05) higher medium diameter DiI+ neurons from inflamed rats than in those from naïve rats. Similarly, post-hoc analysis indicated that resting [Ca2+]i was significantly (p < 0.01) higher medium diameter DiI+ neurons from inflamed rats than in those from naïve rats.