Biological effects and biodistribution of bufotenine on mice


Publication type
Article
Language
English
Access rights
Open Access
Appears in Collections:
Metrics
Abstract
Bufotenine is an alkaloid derived fromserotonin, structurally similar to LSD and psilocin. Thismolecule is able to inhibit the rabies virus infection in in vitro and in vivo models, increasing the survival rate of infected animals. Being a very promising molecule for an incurable disease and because of the fact that there is no consensus regarding its neurological effects, this study aimed to evaluate chronic treatment of bufotenine on behavior, pathophysiology, and pharmacokinetics of mice. Animals were daily treated for 21 consecutive days with 0.63, 1.05, and 2.1 mg/animal/day bufotenine and evaluated by open field test and physiological parameters during all the experiment. After this period, organs were collected for histopathological and biodistribution analysis. Animals treated with bufotenine had mild behavioral alterations compared to the control group, being dose-response relationship. On the other hand, animals showed normal physiological functions and no histological alterations in the organs. With high doses, an inflammatory reaction was observed in the site of injection, but with no cellular damage. The alkaloid could be found in the heart and kidney with all doses and in the lungs and brain with higher doses. These results show that the effective dose, 0.63 mg/day, is safe to be administered in mice, since it did not cause significant effects on the animals' physiology and on the CNS. Higher doses were well tolerated, causing only mild behavioral effects. Thus, bufotenine might be a drug prototype for rabies treatment, an incurable disease.
Reference
Vigerelli H, Sciani JM, Camarano MAE, Sato LA, Antoniazzi MM, Jared C, et al. Biological effects and biodistribution of bufotenine on mice. Biomed Res. Int.. 2018;2018:1032638. doi:10.1155/2018/1032638.
Link to cite this reference
https://repositorio.butantan.gov.br/handle/butantan/2469
Issue Date
2018


Files in This Item:

10.1155:2018:1032638.pdf
Size: 5.57 MB
Format: Adobe PDF
View/Open
Show full item record

The access to the publications deposited in this repository respects the licenses from journals and publishers.