Table 1. Post surgery gene expression analyses by reverse transcription-PCR in central nervous system (CNS) areas and the stomach.
| Gene | Primers | Annealing temperature (°C) | CNS areas | Gastric tissue |
|---|---|---|---|---|
| Ghsr | F:TCTTCGTGGTGGGCATCTCA R:AAGCAGATGGCGAAGTAGCG | 51 | + | |
| Leprb | F:CCAGTGCATCGCCAGGAAA R:ACAGTGAGCTGGGAATGGGC | 55 | + | |
| Mc4r | F:GGCTTCACATTAAGAGGATCGCT R:TTTATGGAACTCCATAGCGCC | 50 | + | |
| Cnr1 | F:AGGGTACTTCCCACAGAAATTC R:CGTGAAGGTGCCCAGCGTGA | 50 | + | + |
| Ghrl | F:TCTTGAGCCCAGAGCACCAGA R:AGTTGCAGAGGAGGCAGAAGC | 50 | + | |
| Mboat4 | F:CTGGGAGGCTCCCTGTGTTCCT R:AAGTCTGCAGCACGGGCCAG | 58 | + | |
| Gapdh | F:TCCCTCAAGATTGTCAGCAA R:AGATCCACAACGGATACATT | 50 | + | + |
Table lists the specific primer sets and annealing temperatures used to detect the expression levels of GHSR, LEPRb, MC4R and CB1R receptors of preproghrelin (Ghrl) and ghrelin O-acyltransferase (Mboat4), and of the housekeeping enzyme GAPDH, in tissues indicated by the plus symbol (+). In all experimental groups, the hypothalamus, hippocampus, cerebral cortex, cerebellum, amygdala and olfactory bulbs were isolated according to stereotactic coordinates and individually processed.27 Gastric tissue was harvested from near the gastroesophageal junction of the remnant gastric tube of sleeve gastrectomized animals and from identical areas in the other study groups.