Literature DB >> 33544325

Sintocalmy, a Passiflora incarnata Based Herbal, Attenuates Morphine Withdrawal in Mice.

Lucas Dos Reis Izolan1, Douglas Marques da Silva1,2, Helena Beatriz Larrosa Oliveira2, Janaína Lucas de Oliveira Salomon2, Caroline Portela Peruzzi3, Solange C Garcia3, Eliane Dallegrave4, Caroline Zanotto5, Elaine Elisabetsky5, Carlos Alberto Gonçalves5, Marcelo Dutra Arbo3, Eduardo Luis Konrath3, Mirna Bainy Leal6,7.   

Abstract

Chronic opioid use changes brain chemistry in areas related to reward processes, memory, decision-making, and addiction. Both neurons and astrocytes are affected, ultimately leading to dependence. Passiflora incarnata L. (Passifloraceae) is the basis of frequently used herbals to manage anxiety and insomnia, with proven central nervous system depressant effects. Anti-addiction properties of P. incarnata have been reported. The aim of this study was to investigate the effect of a commercial extract of Passiflora incarnata (Sintocalmy®, Aché Laboratory) in the naloxone-induced jumping mice model of morphine withdrawal. In addition, glial fibrillary acidic protein (GFAP) and S100 calcium-binding protein B (S100B) levels were assessed in the frontal cortex and hippocampus, and DNA damage was verified on blood cells. In order to improve solubilization a Sintocalmy methanol extract (SME) was used. SME is mainly composed by flavonoids isovitexin and vitexin. The effects of SME 50, 100 and 200 mg/kg (i.p.) were evaluated in the naloxone-induced withdrawal syndrome in mice. SME 50 and SME 100 mg/kg decreased naloxone-induced jumping in morphine-dependent mice without reducing locomotor activity. No alterations were found in GFAP levels, however SME 50 mg/kg prevented the S100B increase in the frontal cortex and DNA damage. This study shows anti-addiction effects for a commercial standardized extract of P. incarnata and suggests the relevance of proper clinical assessment.

Entities:  

Keywords:  DNA damage; Flavonoids; Frontal cortex; P. incarnata standardized extract; S100B; hippocampus

Year:  2021        PMID: 33544325     DOI: 10.1007/s11064-021-03237-w

Source DB:  PubMed          Journal:  Neurochem Res        ISSN: 0364-3190            Impact factor:   3.996


  48 in total

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Journal:  Autophagy       Date:  2013-06-20       Impact factor: 16.016

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Journal:  Neuron       Date:  2011-02-24       Impact factor: 17.173

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Authors:  Anna R Reynolds; Luke A Williams; Meredith A Saunders; Mark A Prendergast
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Authors:  Gertrudis Perea; Mriganka Sur; Alfonso Araque
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Authors:  Puja Seth; Lawrence Scholl; Rose A Rudd; Sarah Bacon
Journal:  MMWR Morb Mortal Wkly Rep       Date:  2018-03-30       Impact factor: 17.586

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