-
Je něco špatně v tomto záznamu ?
Synthetic testosterone derivatives modulate rat P2X2 and P2X4 receptor channel gating
S. Sivcev, B. Slavikova, M. Rupert, M. Ivetic, M. Nekardova, E. Kudova, H. Zemkova,
Jazyk angličtina Země Velká Británie
Typ dokumentu časopisecké články, práce podpořená grantem
NLK
Free Medical Journals
od 1997 do Před 1 rokem
Wiley Free Content
od 1997 do Před 1 rokem
PubMed
31069814
DOI
10.1111/jnc.14718
Knihovny.cz E-zdroje
- MeSH
- gating iontového kanálu účinky léků fyziologie MeSH
- HEK293 buňky MeSH
- krysa rodu rattus MeSH
- lidé MeSH
- potkani Wistar MeSH
- purinergní receptory P2X2 metabolismus MeSH
- purinergní receptory P2X4 metabolismus MeSH
- testosteron farmakologie MeSH
- zvířata MeSH
- Check Tag
- krysa rodu rattus MeSH
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
P2X receptors (P2XRs) are ATP-gated cationic channels that are allosterically modulated by numerous compounds, including steroids and neurosteroids. These compounds may both inhibit and potentiate the activity of P2XRs, but sex steroids such as 17β-estradiol or progesterone are reported to be inactive. Here, we tested a hypothesis that testosterone, another sex hormone, modulates activity of P2XRs. We examined actions of native testosterone and a series of testosterone derivatives on the gating of recombinant P2X2R, P2X4R and P2X7R and native channels expressed in pituitary cells and hypothalamic neurons. The 17β-ester derivatives of testosterone rapidly and positively modulate the 1 µM ATP-evoked currents in P2X2R- and P2X4R-expressing cells, but not agonist-evoked currents in P2X7R-expressing cells. In general, most of the tested testosterone derivatives are more potent modulators than endogenous testosterone. The comparison of chemical structures and whole-cell recordings revealed that their interactions with P2XRs depend on the lipophilicity and length of the alkyl chain at position C-17. Pre-treatment with testosterone butyrate or valerate increases the sensitivity of P2X2R and P2X4R to ATP by several fold, reduces the rate of P2X4R desensitization, accelerates resensitization, and enhances ethidium uptake by P2X4R. Native channels are also potentiated by testosterone derivatives, while endogenously expressed GABA receptors type A are inhibited. The effect of ivermectin, a P2X4R-specific allosteric modulator, on deactivation is antagonized by testosterone derivatives in a concentration-dependent manner. Together, our results provide evidence for potentiation of particular subtypes of P2XRs by testosterone derivatives and suggest a potential role of ivermectin binding site for steroid-induced modulation. OPEN SCIENCE BADGES: This article has received a badge for *Open Materials* because it provided all relevant information to reproduce the study in the manuscript. The complete Open Science Disclosure form for this article can be found at the end of the article. More information about the Open Practices badges can be found at https://cos.io/our-services/open-science-badges/.
Institute of Organic Chemistry and Biochemistry Czech Academy of Sciences Prague Czech Republic
Institute of Physiology Czech Academy of Sciences Prague Czech Republic
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc20006384
- 003
- CZ-PrNML
- 005
- 20200525100339.0
- 007
- ta
- 008
- 200511s2019 xxk f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1111/jnc.14718 $2 doi
- 035 __
- $a (PubMed)31069814
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxk
- 100 1_
- $a Sivcev, Sonja $u Institute of Physiology, Czech Academy of Sciences, Prague, Czech Republic. Faculty of Science, Charles University, Prague, Czech Republic.
- 245 10
- $a Synthetic testosterone derivatives modulate rat P2X2 and P2X4 receptor channel gating / $c S. Sivcev, B. Slavikova, M. Rupert, M. Ivetic, M. Nekardova, E. Kudova, H. Zemkova,
- 520 9_
- $a P2X receptors (P2XRs) are ATP-gated cationic channels that are allosterically modulated by numerous compounds, including steroids and neurosteroids. These compounds may both inhibit and potentiate the activity of P2XRs, but sex steroids such as 17β-estradiol or progesterone are reported to be inactive. Here, we tested a hypothesis that testosterone, another sex hormone, modulates activity of P2XRs. We examined actions of native testosterone and a series of testosterone derivatives on the gating of recombinant P2X2R, P2X4R and P2X7R and native channels expressed in pituitary cells and hypothalamic neurons. The 17β-ester derivatives of testosterone rapidly and positively modulate the 1 µM ATP-evoked currents in P2X2R- and P2X4R-expressing cells, but not agonist-evoked currents in P2X7R-expressing cells. In general, most of the tested testosterone derivatives are more potent modulators than endogenous testosterone. The comparison of chemical structures and whole-cell recordings revealed that their interactions with P2XRs depend on the lipophilicity and length of the alkyl chain at position C-17. Pre-treatment with testosterone butyrate or valerate increases the sensitivity of P2X2R and P2X4R to ATP by several fold, reduces the rate of P2X4R desensitization, accelerates resensitization, and enhances ethidium uptake by P2X4R. Native channels are also potentiated by testosterone derivatives, while endogenously expressed GABA receptors type A are inhibited. The effect of ivermectin, a P2X4R-specific allosteric modulator, on deactivation is antagonized by testosterone derivatives in a concentration-dependent manner. Together, our results provide evidence for potentiation of particular subtypes of P2XRs by testosterone derivatives and suggest a potential role of ivermectin binding site for steroid-induced modulation. OPEN SCIENCE BADGES: This article has received a badge for *Open Materials* because it provided all relevant information to reproduce the study in the manuscript. The complete Open Science Disclosure form for this article can be found at the end of the article. More information about the Open Practices badges can be found at https://cos.io/our-services/open-science-badges/.
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a HEK293 buňky $7 D057809
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a gating iontového kanálu $x účinky léků $x fyziologie $7 D015640
- 650 _2
- $a krysa rodu Rattus $7 D051381
- 650 _2
- $a potkani Wistar $7 D017208
- 650 _2
- $a purinergní receptory P2X2 $x metabolismus $7 D058476
- 650 _2
- $a purinergní receptory P2X4 $x metabolismus $7 D058848
- 650 _2
- $a testosteron $x farmakologie $7 D013739
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Slavikova, Barbora $u Institute of Organic Chemistry and Biochemistry, Czech Academy of Sciences, Prague, Czech Republic.
- 700 1_
- $a Rupert, Marian $u Institute of Physiology, Czech Academy of Sciences, Prague, Czech Republic. 1st Faculty of Medicine, Charles University, Prague, Czech Republic.
- 700 1_
- $a Ivetic, Milorad $u Institute of Physiology, Czech Academy of Sciences, Prague, Czech Republic.
- 700 1_
- $a Nekardova, Michaela $u Institute of Organic Chemistry and Biochemistry, Czech Academy of Sciences, Prague, Czech Republic. Faculty of Mathematics and Physics, Charles University, Prague, Czech Republic.
- 700 1_
- $a Kudova, Eva $u Institute of Organic Chemistry and Biochemistry, Czech Academy of Sciences, Prague, Czech Republic.
- 700 1_
- $a Zemkova, Hana $u Institute of Physiology, Czech Academy of Sciences, Prague, Czech Republic.
- 773 0_
- $w MED00002832 $t Journal of neurochemistry $x 1471-4159 $g Roč. 150, č. 1 (2019), s. 28-43
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/31069814 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20200511 $b ABA008
- 991 __
- $a 20200525100340 $b ABA008
- 999 __
- $a ok $b bmc $g 1525242 $s 1096440
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2019 $b 150 $c 1 $d 28-43 $e 20190618 $i 1471-4159 $m Journal of neurochemistry $n J Neurochem $x MED00002832
- LZP __
- $a Pubmed-20200511