Evidence for the involvement of spinal cord-inhibitory and cytokines-modulatory mechanisms in the anti-hyperalgesic effect of hecogenin acetate, a steroidal sapogenin-acetylated, in mice

Hecogenin is a steroidal sapogenin largely drawn from the plants of the genus Agave, commonly known as 'sisal', and is one of the important precursors used by the pharmaceutical industry for the synthesis of steroid hormones. Hecogenin acetate (HA) is a steroidal sapogenin-acetylated that...

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Published in:Molecules (Basel, Switzerland) Vol. 19; no. 6; pp. 8303 - 8316
Main Authors: Quintans, Jullyana S S, Barreto, Rosana S S, de Lucca, Jr, Waldecy, Villarreal, Cristiane F, Kaneto, Carla M, Soares, Milena B P, Branco, Alexsandro, Almeida, Jackson R G S, Taranto, Alex G, Antoniolli, Angelo R, Freitas, Rivelilson M, Quintans, Jr, Lucindo J
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Abstract Hecogenin is a steroidal sapogenin largely drawn from the plants of the genus Agave, commonly known as 'sisal', and is one of the important precursors used by the pharmaceutical industry for the synthesis of steroid hormones. Hecogenin acetate (HA) is a steroidal sapogenin-acetylated that produces antinociceptive activity. Thus, we evaluate the antihyperalgesic profile of HA in mice in inflammatory models, as well as its possible involvement with c-fos expression on spinal cord area and cytokines to produces analgesic profile. Acute pretreatment with HA (5, 10, or 20 mg/kg; i.p.) inhibited the development of mechanical hyperalgesia induced by carrageenan, TNF-α, dopamine and PGE2. Additionally, the immunofluorescence data demonstrated that acute pretreatment with HA, at all doses tested, significantly inhibited Fos-like expression in the spinal cord dorsal horn normally observed after carrageenan-inflammation. Moreover, HA did not affect the motor performance of the mice as tested in the Rota rod test. This antinociceptive profile seems to be related, at least in part, to a reduction of pro-inflammatory cytokines, as IL-1β. The present results suggest that HA attenuates mechanical hyperalgesia by blocking the neural transmission of pain at the spinal cord levels and by cytokines-inhibitory mechanisms.
AbstractList Hecogenin is a steroidal sapogenin largely drawn from the plants of the genus Agave, commonly known as ‘sisal’, and is one of the important precursors used by the pharmaceutical industry for the synthesis of steroid hormones. Hecogenin acetate (HA) is a steroidal sapogenin-acetylated that produces antinociceptive activity. Thus, we evaluate the antihyperalgesic profile of HA in mice in inflammatory models, as well as its possible involvement with c-fos expression on spinal cord area and cytokines to produces analgesic profile. Acute pretreatment with HA (5, 10, or 20 mg/kg; i.p.) inhibited the development of mechanical hyperalgesia induced by carrageenan, TNF-α, dopamine and PGE2. Additionally, the immunofluorescence data demonstrated that acute pretreatment with HA, at all doses tested, significantly inhibited Fos-like expression in the spinal cord dorsal horn normally observed after carrageenan-inflammation. Moreover, HA did not affect the motor performance of the mice as tested in the Rota rod test. This antinociceptive profile seems to be related, at least in part, to a reduction of pro-inflammatory cytokines, as IL-1β. The present results suggest that HA attenuates mechanical hyperalgesia by blocking the neural transmission of pain at the spinal cord levels and by cytokines-inhibitory mechanisms.
Hecogenin is a steroidal sapogenin largely drawn from the plants of the genus Agave, commonly known as 'sisal', and is one of the important precursors used by the pharmaceutical industry for the synthesis of steroid hormones. Hecogenin acetate (HA) is a steroidal sapogenin-acetylated that produces antinociceptive activity. Thus, we evaluate the antihyperalgesic profile of HA in mice in inflammatory models, as well as its possible involvement with c-fos expression on spinal cord area and cytokines to produces analgesic profile. Acute pretreatment with HA (5, 10, or 20 mg/kg; i.p.) inhibited the development of mechanical hyperalgesia induced by carrageenan, TNF- alpha , dopamine and PGE2. Additionally, the immunofluorescence data demonstrated that acute pretreatment with HA, at all doses tested, significantly inhibited Fos-like expression in the spinal cord dorsal horn normally observed after carrageenan-inflammation. Moreover, HA did not affect the motor performance of the mice as tested in the Rota rod test. This antinociceptive profile seems to be related, at least in part, to a reduction of pro-inflammatory cytokines, as IL-1 beta . The present results suggest that HA attenuates mechanical hyperalgesia by blocking the neural transmission of pain at the spinal cord levels and by cytokines-inhibitory mechanisms.
Author Freitas, Rivelilson M
Villarreal, Cristiane F
Quintans, Jr, Lucindo J
Taranto, Alex G
Antoniolli, Angelo R
Barreto, Rosana S S
Soares, Milena B P
Almeida, Jackson R G S
de Lucca, Jr, Waldecy
Kaneto, Carla M
Branco, Alexsandro
Quintans, Jullyana S S
AuthorAffiliation 5 Colegiado de Ciências Farmacêuticas. Universidade Federal do Vale do São Francisco, Petrolina, CEP 56.304-205, Pernambuco, Brazil; E-Mail: jackson.guedes@univasf.edu.br
4 Colegiado de Ciências Farmacêuticas, Universidade Estadual de Feira de Santana, Feira de Santana, Bahia, CEP 44.036-900, Brazil; E-Mail: branco@uefs.br
7 Departamento de Farmácia, Universidade Federal do Piauí, Teresina, Piauí, CEP 64.049-550, Brazil; E-Mail: rivelilson@pq.cnpq.br
6 Curso de Farmácia, Universidade Federal de São João Del-Rei, Campus Centro Oeste Dona Lindu, Divinópolis, Minas Gerais, CEP 35.501-296, Brazil; E-Mail: proftaranto@hotmail.com
1 Departamento de Fisiologia. Universidade Federal de Sergipe-UFS, Av. Marechal Rondom, s/n, São Cristóvão, Sergipe, CEP 49.000-100, Brazil; E-Mails: jullyanas@yahoo.com.br (J.S.S.Q.); rosanasfisio@hotmail.com (R.S.S.B.); wlucca1@gmail.com (W.L.J.); aroberto@ufs.br (A.R.A.)
3 Centro de Biotecnologia e Terapia Celular, Hospital São Rafael, Salvador, Bahia, CEP 41.253-190
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– name: 3 Centro de Biotecnologia e Terapia Celular, Hospital São Rafael, Salvador, Bahia, CEP 41.253-190, Brazil; E-Mails: carlakenato@bahia.fiocruz.br (C.M.K.); milena@bahia.fiocruz.br (M.B.P.S.)
– name: 1 Departamento de Fisiologia. Universidade Federal de Sergipe-UFS, Av. Marechal Rondom, s/n, São Cristóvão, Sergipe, CEP 49.000-100, Brazil; E-Mails: jullyanas@yahoo.com.br (J.S.S.Q.); rosanasfisio@hotmail.com (R.S.S.B.); wlucca1@gmail.com (W.L.J.); aroberto@ufs.br (A.R.A.)
– name: 2 Faculdade de Farmácia, Universidade Federal da Bahia, Salvador, Bahia, CEP 40.170-115, Brazil; E-Mail: cfv@conveniado.bahia.fiocruz.br
– name: 4 Colegiado de Ciências Farmacêuticas, Universidade Estadual de Feira de Santana, Feira de Santana, Bahia, CEP 44.036-900, Brazil; E-Mail: branco@uefs.br
Author_xml – sequence: 1
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  organization: Departamento de Fisiologia. Universidade Federal de Sergipe-UFS, Av. Marechal Rondom, s/n, São Cristóvão, Sergipe, CEP 49.000-100, Brazil. jullyanas@yahoo.com.br
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  organization: Departamento de Fisiologia. Universidade Federal de Sergipe-UFS, Av. Marechal Rondom, s/n, São Cristóvão, Sergipe, CEP 49.000-100, Brazil. wlucca1@gmail.com
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  givenname: Cristiane F
  surname: Villarreal
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  email: cfv@conveniado.bahia.fiocruz.br
  organization: Faculdade de Farmácia, Universidade Federal da Bahia, Salvador, Bahia, CEP 40.170-115, Brazil. cfv@conveniado.bahia.fiocruz.br
– sequence: 5
  givenname: Carla M
  surname: Kaneto
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  email: carlakenato@bahia.fiocruz.br
  organization: Centro de Biotecnologia e Terapia Celular, Hospital São Rafael, Salvador, Bahia, CEP 41.253-190, Brazil. carlakenato@bahia.fiocruz.br
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  givenname: Milena B P
  surname: Soares
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  email: milena@bahia.fiocruz.br
  organization: Centro de Biotecnologia e Terapia Celular, Hospital São Rafael, Salvador, Bahia, CEP 41.253-190, Brazil. milena@bahia.fiocruz.br
– sequence: 7
  givenname: Alexsandro
  surname: Branco
  fullname: Branco, Alexsandro
  email: branco@uefs.br
  organization: Colegiado de Ciências Farmacêuticas, Universidade Estadual de Feira de Santana, Feira de Santana, Bahia, CEP 44.036-900, Brazil. branco@uefs.br
– sequence: 8
  givenname: Jackson R G S
  surname: Almeida
  fullname: Almeida, Jackson R G S
  email: jackson.guedes@univasf.edu.br
  organization: Colegiado de Ciências Farmacêuticas. Universidade Federal do Vale do São Francisco, Petrolina, CEP 56.304-205, Pernambuco, Brazil. jackson.guedes@univasf.edu.br
– sequence: 9
  givenname: Alex G
  surname: Taranto
  fullname: Taranto, Alex G
  email: proftaranto@hotmail.com
  organization: Curso de Farmácia, Universidade Federal de São João Del-Rei, Campus Centro Oeste Dona Lindu, Divinópolis, Minas Gerais, CEP 35.501-296, Brazil. proftaranto@hotmail.com
– sequence: 10
  givenname: Angelo R
  surname: Antoniolli
  fullname: Antoniolli, Angelo R
  email: aroberto@ufs.br
  organization: Departamento de Fisiologia. Universidade Federal de Sergipe-UFS, Av. Marechal Rondom, s/n, São Cristóvão, Sergipe, CEP 49.000-100, Brazil. aroberto@ufs.br
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  givenname: Rivelilson M
  surname: Freitas
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  surname: Quintans, Jr
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  organization: Departamento de Fisiologia. Universidade Federal de Sergipe-UFS, Av. Marechal Rondom, s/n, São Cristóvão, Sergipe, CEP 49.000-100, Brazil. lucindojr@gmail.com
BackLink https://www.ncbi.nlm.nih.gov/pubmed/24950436$$D View this record in MEDLINE/PubMed
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Snippet Hecogenin is a steroidal sapogenin largely drawn from the plants of the genus Agave, commonly known as 'sisal', and is one of the important precursors used by...
Hecogenin is a steroidal sapogenin largely drawn from the plants of the genus Agave, commonly known as ‘sisal’, and is one of the important precursors used by...
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StartPage 8303
SubjectTerms Agave
Analgesics
Animals
c-fos
Carrageenan - toxicity
Cytokines
Cytokines - metabolism
Drug dosages
Electronic mail systems
FDA approval
hecogenin acetate
Hormones
Hyperalgesia
Hyperalgesia - chemically induced
Hyperalgesia - prevention & control
IL-1β
Interleukin-1beta - metabolism
Male
Mice
Natural products
Nonsteroidal anti-inflammatory drugs
Pain
Pharmaceutical industry
Spinal cord
Spinal Cord - drug effects
Spiro Compounds - pharmacology
Spiro Compounds - therapeutic use
steroidal sapogenin
Steroids
Steroids - pharmacology
Steroids - therapeutic use
Tumor Necrosis Factor-alpha - metabolism
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Title Evidence for the involvement of spinal cord-inhibitory and cytokines-modulatory mechanisms in the anti-hyperalgesic effect of hecogenin acetate, a steroidal sapogenin-acetylated, in mice
URI https://www.ncbi.nlm.nih.gov/pubmed/24950436
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Volume 19
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