Ative and timed food intake 0.5, 1, 2,

Ative and timed food intake 0.5, 1, 2, 1516647 4 and 24 h following treatment in fasted mice. During the first half hour, 0.5 and 1 nmol of NPS dose-dependently inhibited food intake versus i.c.v. vehicle-treated mice (p,0.01 and p,0.001, respectively; Fig. 6A and B). Compared with vehicle, mice treated with NPS showed aNPS Facilitates Olfactory FunctionTable 1. Number of Fos-ir neurons in the VTT, ACo and LEnt after i.c.v. injection of NPS or vehicle.Number of Fos-ir neurons Groups NPS (n = 4) Vehicle (n = 5) VTT 297.00613.22 * 100.0065.46 ACo 384.00611.58 * 204.40615.91 LEnt 1583.50643.52 * 850.00619.Values are purchase Hexaconazole expressed as means 6 SEM. Cells were counted bilaterally per animal. * p,0.001, compared with vehicle-treated mice. Data were analyzed by independent student’s t-test. doi:10.1371/journal.pone.0062089.tsignificant reduction of food intake in the 0-0.5 h during 24 hours period (Fig. 6). However, during the second hour following treatment, the mice injected with NPS ate significantly more than the control (p,0.01; Fig. 6B).Figure 8. NPS-induced Fos-ir neurons bearing NPSR in the AON and Pir. Photomicrographs show Fos-ir neurons in the AON (A) and Pir (D) after NPS i.c.v. administration, NPSR-ir neurons in the AON (B) and Pir (E), and the co-expression of Fos-ir and NPSR-ir neurons in the AON (C) and Pir (F), respectively. Arrow (C and F) show the co-expression of Fos-ir and NPSR-ir neurons. Bar = 50 mm. doi:10.1371/journal.pone.0062089.gNPS induced c-Fos labeling in the olfactory cortexIn the olfactory cortex, central administration of NPS (0.5 nmol) induced a large number of Fos-ir neurons in the AON (Fig. 7A) and Pir (Fig. 7C) and a moderate number of Fos-ir neurons in the VTT, the ACo and LEnt (Table. 1), and the numbers were significantly more than that seen in vehicle injection. In the present study, we focused on the AON and Pir areas because they are well-known to play a key role in olfactory function and regulation [28]. In comparison with vehicle-treated mice, NPS significantly increased the number of Fos-ir neurons by 13.2-fold (22366199 vs. 169615) in the AON (Fig. 7E) and 8.6-fold (1113649 vs. 128616) in the Pir (Fig. 7F). In addition, NPS also induced an increase in the number of Fos-ir neurons in the motor and somatosensory cortex, amygdala, periaqueductal gray, tuberomammillary nucleus, arcuate hypothalamic nucleus, and the perifornical nucleus and the lateral hypothalamic area (data not shown). FMRFamide are also involved in the modulation of olfactory function [34]. Clark et al. reported that NPS is originated from the Kolliker-Fuse nucleus and pericoerulear area of the mouse ?brainstem and that NPSR mRNA is JSI124 cost highly expressed in the olfactory cortex [2]. Taken together, NPS projections from the Kolliker-Fuse nucleus and pericoerulear area of the mouse ?brainstem to the olfactory cortex may provide mechanistic basis for its regulation of olfactory function. Olfaction is of great importance to mammals’ survival, and influences a variety of social activities, including recognition, mate selection, fear responses to predator odors and food intake, especially in rodents [23,24]. In the present study, when 0.5 or 1 nmol of NPS were respectively i.c.v. administrated in fasted mice, food intake was dose-dependently reduced during the first half hour compared with vehicle-treated mice (Fig. 6). These findings are consistent with those of earlier observations in which NPS inhibits food intake in mice and rats [9,35?7]. The mechanis.Ative and timed food intake 0.5, 1, 2, 1516647 4 and 24 h following treatment in fasted mice. During the first half hour, 0.5 and 1 nmol of NPS dose-dependently inhibited food intake versus i.c.v. vehicle-treated mice (p,0.01 and p,0.001, respectively; Fig. 6A and B). Compared with vehicle, mice treated with NPS showed aNPS Facilitates Olfactory FunctionTable 1. Number of Fos-ir neurons in the VTT, ACo and LEnt after i.c.v. injection of NPS or vehicle.Number of Fos-ir neurons Groups NPS (n = 4) Vehicle (n = 5) VTT 297.00613.22 * 100.0065.46 ACo 384.00611.58 * 204.40615.91 LEnt 1583.50643.52 * 850.00619.Values are expressed as means 6 SEM. Cells were counted bilaterally per animal. * p,0.001, compared with vehicle-treated mice. Data were analyzed by independent student’s t-test. doi:10.1371/journal.pone.0062089.tsignificant reduction of food intake in the 0-0.5 h during 24 hours period (Fig. 6). However, during the second hour following treatment, the mice injected with NPS ate significantly more than the control (p,0.01; Fig. 6B).Figure 8. NPS-induced Fos-ir neurons bearing NPSR in the AON and Pir. Photomicrographs show Fos-ir neurons in the AON (A) and Pir (D) after NPS i.c.v. administration, NPSR-ir neurons in the AON (B) and Pir (E), and the co-expression of Fos-ir and NPSR-ir neurons in the AON (C) and Pir (F), respectively. Arrow (C and F) show the co-expression of Fos-ir and NPSR-ir neurons. Bar = 50 mm. doi:10.1371/journal.pone.0062089.gNPS induced c-Fos labeling in the olfactory cortexIn the olfactory cortex, central administration of NPS (0.5 nmol) induced a large number of Fos-ir neurons in the AON (Fig. 7A) and Pir (Fig. 7C) and a moderate number of Fos-ir neurons in the VTT, the ACo and LEnt (Table. 1), and the numbers were significantly more than that seen in vehicle injection. In the present study, we focused on the AON and Pir areas because they are well-known to play a key role in olfactory function and regulation [28]. In comparison with vehicle-treated mice, NPS significantly increased the number of Fos-ir neurons by 13.2-fold (22366199 vs. 169615) in the AON (Fig. 7E) and 8.6-fold (1113649 vs. 128616) in the Pir (Fig. 7F). In addition, NPS also induced an increase in the number of Fos-ir neurons in the motor and somatosensory cortex, amygdala, periaqueductal gray, tuberomammillary nucleus, arcuate hypothalamic nucleus, and the perifornical nucleus and the lateral hypothalamic area (data not shown). FMRFamide are also involved in the modulation of olfactory function [34]. Clark et al. reported that NPS is originated from the Kolliker-Fuse nucleus and pericoerulear area of the mouse ?brainstem and that NPSR mRNA is highly expressed in the olfactory cortex [2]. Taken together, NPS projections from the Kolliker-Fuse nucleus and pericoerulear area of the mouse ?brainstem to the olfactory cortex may provide mechanistic basis for its regulation of olfactory function. Olfaction is of great importance to mammals’ survival, and influences a variety of social activities, including recognition, mate selection, fear responses to predator odors and food intake, especially in rodents [23,24]. In the present study, when 0.5 or 1 nmol of NPS were respectively i.c.v. administrated in fasted mice, food intake was dose-dependently reduced during the first half hour compared with vehicle-treated mice (Fig. 6). These findings are consistent with those of earlier observations in which NPS inhibits food intake in mice and rats [9,35?7]. The mechanis.