Table 1.
Primers for the real time qPCR analyses.
Figure 1.
Food Intake measures in rats after icv treatment with ghrelin/vehicle (6 µg/rat) and ip treatment with rimonabant (3 mg/kg ip)/vehicle under different nutritional statuses: A) Ad libitum fed, B) nocturnal fasting, c) animals subjected to overnight fasting and previously subjected to surgical vagotomy.
*vs control, #vs. rimonabant+ghrelin.
Figure 2.
Immunohistochemical studies of the locatizations of ghrelin (A) and CB1 (B) in gastric tissue from ad libitum fed rats.
Inmunoreactivities for both antibodies were found in isolated neuroendocrine cells primarily that were primary located at the bottom of the gastric glands. Labeling of neuroendocrine cells with synaptophysin is shown in panel (C). The corresponding negative control (D). Magnification 40x.
Figure 3.
Gastric ghrelin secretion from tissue explants obtained from ad libitum fed animals (A) or 36-hour fasted animals (B) and plasma ghrelin levels from ad libitum fed animals (C) or 36-hour fasted animals (D) under different in vivo treatments (control/rimonabant), and surgical procedures (vagotomy/sham operated).
Gastric ghrelin secretion from tissue explants from ad libitum fed animals (E) or 36-hour fasted animals (F) under different in vitro treatments (control/rimonabant) and surgical procedures (vagotomy/sham operated). *vs control.
Figure 4.
mRNA expression levels measured by real-time PCR for ghrelin in ad libitum fed animals (A) or 36-hour fasted animals (B).
Ghrelin protein levels and representative Western blot from the mucosa from ad libitum fed animals (C) or 36-hours fasted animals (D). Animals that received different in vivo treatments (control/rimonabant) and surgical procedures (vagotomy/sham-operated). C: control, R: rimonabant, V: vagotomy; V+R: vagotomy+rimonabant. CB1 receptor mRNA levels in the gastric mucosae of ad libitum fed animals (E) or 36-hour fasted animals (F) and animals that received different in vivo treatments (control/rimonabant) and surgical procedures (vagotomy/sham operated). *vs control.
Figure 5.
Measures of pmTOR/mTOR levels in gastric mucosa and representative Western blots from animals in the fasting state treated with ip rimonabant and/or ip rapamycin chronically for 1 week (A).
Phospho-S6K1/S6K1 in gastric mucosae from animals in the fasting state treated with rimonabant ip and/or rapamycin ip chronically for 1 week (B). The results are expressed as percentages over control (phospho-S6K1/S6K1). *p<0.05, vs control; #p<0.05 vs rimonabant. C: control, R: rimonabant, Ra: rapamycin; Ra+R: rapamycin+rimonabant.
Figure 6.
Gastric ghrelin secretion (A).
Ghrelin mRNA levels measured by real-time PCR in the gastric mucosae (B) and plasma ghrelin levels (C) from animals in fasting states treated with ip rimonabant and/or ip rapamycin chronically for 1 week.
Figure 7.
Gastric ghrelin secretion from tissue explants (A) and plasma ghrelin levels (B) obtained from 36-hour fasted animals that received in vivo treatment with AM281 (3 mg/Kg ip).
**p<0.01.
Figure 8.
Measures of pmTOR/mTOR in the gastric mucosae and representative Western blots from animals in the fasting state treated with ip AM281 or vehicle (A).
Phospho-S6K1/S6K1 in the gastric mucosae and representative Western blots from animals in the fasting state treated with ip AM281 or vehicle (control) (B). The results are expressed as percentage over control (phospho-S6K1/S6K1). *p<0.05.