PMID- 34479060 OWN - NLM STAT- MEDLINE DCOM- 20211102 LR - 20220531 IS - 1872-8464 (Electronic) IS - 0165-5876 (Linking) VI - 150 DP - 2021 Nov TI - Protective role of lycopene in experimental allergic rhinitis in rats. PG - 110905 LID - S0165-5876(21)00298-6 [pii] LID - 10.1016/j.ijporl.2021.110905 [doi] AB - OBJECTIVE: We investigate whether lycopene has a protective effect in an experimental rat model of allergic rhinitis. METHODS: Experimental animals (65 rats) were randomized to 7 groups (Sham-Control, Lycopene 10 mg/kg/day, Lycopene 20 mg/kg/day, Intranasal lycopene drops, Intranasal steroid, Corn oil, Allergic Rhinitis). Rats were sensitized by administering of ovalbumin intraperitoneally and intranasally. In addition to ovalbumin; lycopene, corn oil and steroids were given to the relevant groups. Nasal symptom scores of the rats were recorded throughout the study. At end of the study, after intracardiac blood sample collection, all rats were sacrificed, and nasal tissues were examined histopathologically. Serum total immunoglobulin E (IgE) and ovalbumin (OVA) specific IgE were studied from all rats before and after the study. RESULTS: There was a statistically significant increase (p < 0.05) in OVA specific IgE values measured before and after the study in all groups except the sham group. In serum total IgE values; there was a statistically significant increase after treatment in allergic rhinitis, corn oil, lycopene 10 mg and intranasal lycopene drops group, but other groups did not show any significant change. Histopathological study with hematoxylin-eosin staining and cyclooxygenase-2 (COX-2), matrix metalloproteinase-9 (MMP-9), vasoactive intestinal peptide (VIP) expression found that lycopene suppresses inflammation with both nasal administration and increased dose. Nasal symptom scores were observed to decrease significantly in all lycopene and steroid groups compared to allergic rihinits and corn groups. CONCLUSION: It was determined that lycopene were effective in the treatment of allergic rhinitis, and this effect was found to be stronger with increasing doses of lycopene. CI - Copyright (c) 2021 Elsevier B.V. All rights reserved. FAU - Polat, Halil AU - Polat H AD - Yozgat City Hospital, Department of ENT, Turkey. Electronic address: drhalilpolat5@gmail.com. FAU - Sagit, Mustafa AU - Sagit M AD - Kayseri Training and Research Hospital, Department of ENT, Turkey. FAU - Gurgen, Seren Gulsen AU - Gurgen SG AD - Celal Bayar University School of Vocational Health Service, Department of Histology and Embryology, Turkey. FAU - Yasar, Mehmet AU - Yasar M AD - Kayseri Training and Research Hospital, Department of ENT, Turkey. FAU - Ozcan, Ibrahim AU - Ozcan I AD - Kayseri Training and Research Hospital, Department of ENT, Turkey. LA - eng PT - Journal Article PT - Randomized Controlled Trial, Veterinary DEP - 20210830 PL - Ireland TA - Int J Pediatr Otorhinolaryngol JT - International journal of pediatric otorhinolaryngology JID - 8003603 RN - 37341-29-0 (Immunoglobulin E) RN - 9006-59-1 (Ovalbumin) RN - SB0N2N0WV6 (Lycopene) SB - IM MH - Animals MH - Disease Models, Animal MH - Immunoglobulin E MH - Lycopene MH - Mice MH - Mice, Inbred BALB C MH - Nasal Mucosa MH - Ovalbumin MH - Rats MH - *Rhinitis, Allergic/drug therapy OTO - NOTNLM OT - Allergic OT - Animal model OT - Experimental OT - Lycopene OT - Ovalbumin OT - Rat OT - Rhinitis OT - Steroid EDAT- 2021/09/04 06:00 MHDA- 2021/11/03 06:00 CRDT- 2021/09/03 20:22 PHST- 2021/01/03 00:00 [received] PHST- 2021/07/08 00:00 [revised] PHST- 2021/08/28 00:00 [accepted] PHST- 2021/09/04 06:00 [pubmed] PHST- 2021/11/03 06:00 [medline] PHST- 2021/09/03 20:22 [entrez] AID - S0165-5876(21)00298-6 [pii] AID - 10.1016/j.ijporl.2021.110905 [doi] PST - ppublish SO - Int J Pediatr Otorhinolaryngol. 2021 Nov;150:110905. doi: 10.1016/j.ijporl.2021.110905. Epub 2021 Aug 30.