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. 1999 Mar 16;96(6):3206–3210. doi: 10.1073/pnas.96.6.3206

Table 1.

Elemental concentrations in secretory vesicles of isolated rat neurohypophysical nerve endings

Condition and location Conc., mmol/kg dry weight
Na/S regression R2 (probability) Na/Cl regression R2(probability)
n Na S Cl Ca
Control
 Peripheral vesicles 64 60  ±  6 836  ±  22 50  ±  4 3.3  ±  0.8 0.0002 (P = 0.92) 0.38 (P = 0.0001)
 Internal vesicles 94 38  ±  3 814  ±  20 50  ±  3 4.2  ±  0.9 0.0005 (P = 0.83) 0.21 (P = 0.0001)
Stimulated 6 min
 Peripheral vesicles 84 99  ±  7** 750  ±  18* 57  ±  5 4.9  ±  0.7* 0.11 (P = 0.001) 0.05 (P = 0.04)
 Internal vesicles 66 50  ±  4* 814  ±  19 46  ±  5 4.9  ±  1.1 0.008 (P = 0.47) 0.03 (P = 0.12)
Stimulated 20 min
 Peripheral vesicles 67 71  ±  6* 775  ±  18* 74  ±  5** 5.6  ±  1.0* 0.004 (P = 0.61) 0.09 (P = 0.01)
 Internal vesicles 101 33  ±  2 808  ±  18 62  ±  3** 6.9  ±  1.1* 0.006 (P = 0.44) 0.006 (P = 0.42)

Data are given as mean ± SEM. Column n is the number of vesicles analyzed; the number of endings analyzed ranged from 33 to 35 per experimental condition. Concentrations in mmol/kg dry weight can be converted to mmol/kg wet tissue by dividing by a factor of 2 (see Materials and Methods). Concentrations were also obtained for several other elements as follows (range in parentheses): Mg (36–45); P (126–149); K (98–137). The correlation, when significant, is negative for Na/S and positive for Na/Cl. The R2 probability was obtained by ANOVA. Significantly different from control values by Mann–Whitney test: ∗, P < 0.05; ∗∗, P < 0.001.