PMID- 29552054 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20201001 IS - 1735-0328 (Print) IS - 1726-6890 (Electronic) IS - 1726-6882 (Linking) VI - 16 IP - 4 DP - 2017 Fall TI - Study of the Role of CREB, BDNF, and VGF Neuropeptide in Long Term Antidepressant Activity of Crocin in the Rat Cerebellum. PG - 1452-1462 AB - Antidepressant activity of crocin, saffron main component, has been established before. Based on previous study, it is suggested that elevation in the levels of BDNF (brain-derived neurotrophic factor), CREB (cAMP response element binding) and VGF neuropeptide could be considered as one probable molecular mechanisms involved in antidepressant activity of long term crocin administration in the rat hippocampus. In this study we further investigated whether the antidepressant activity of crocin in long term administration was associated with alteration in these factors in the rat cerebellum. Crocin (12.5, 25 and 50 mg/kg/day) and imipramine (10 mg/kg/day) were administered interaperitoneally for 21 days to rats. At the end of experiment, animals were sacrificed and cerebellums were dissected. BDNF, VGF, CREB, and phospho-CREB (P-CREB) protein and mRNA levels in the rat cerebellum were evaluated using Western blot and quantitative reverse transcription-polymerase chain reaction (qRT-PCR). In the current study significant increases in mRNA and protein levels of VGF, CREB and (BDNF) in long term crocin treatment were not observed in the rat cerebellum. Although a slight increase was observed in protein level of P-CREB compared to normal saline, but it was not significant. It is concluded that antidepressant activity of crocin might be partially mediated to CREB. Moreover, other factors rather than BDNF and VGF neuropeptides may alter following long term crocin treatment in the cerebellum. To understand the precise mechanism of crocin antidepressant effects in the cerebellum, longer duration of crocin treatment in further studies is recommended. FAU - Razavi, Bibi Marjan AU - Razavi BM AD - Targeted Drug Delivery Research Center, Mashhad University of Medical Sciences, Mashhad, Iran. AD - Department of Pharmacodynamy and Toxicology, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran. FAU - Sadeghi, Mahdieh AU - Sadeghi M AD - Department of Pharmacodynamy and Toxicology, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran. FAU - Abnous, Khalil AU - Abnous K AD - Pharmaceutical Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, Iran. AD - Department of Medicinal Chemistry, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran. FAU - Vahdati Hasani, Faezeh AU - Vahdati Hasani F AD - Department of Pharmacodynamy and Toxicology, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran. FAU - Hosseinzadeh, Hossein AU - Hosseinzadeh H AD - Pharmaceutical Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, Iran. AD - Department of Pharmacodynamy and Toxicology, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran. LA - eng PT - Journal Article PL - Netherlands TA - Iran J Pharm Res JT - Iranian journal of pharmaceutical research : IJPR JID - 101208407 PMC - PMC5843307 OTO - NOTNLM OT - BDNF OT - CREB OT - Cerebellum OT - Crocin OT - Depression OT - P-CREB OT - Saffron EDAT- 2018/03/20 06:00 MHDA- 2018/03/20 06:01 PMCR- 2017/09/01 CRDT- 2018/03/20 06:00 PHST- 2018/03/20 06:00 [entrez] PHST- 2018/03/20 06:00 [pubmed] PHST- 2018/03/20 06:01 [medline] PHST- 2017/09/01 00:00 [pmc-release] AID - IJPR-16-1452 [pii] PST - ppublish SO - Iran J Pharm Res. 2017 Fall;16(4):1452-1462.