000 | 03945nlm1a2200565 4500 | ||
---|---|---|---|
001 | 667439 | ||
005 | 20231030042111.0 | ||
035 | _a(RuTPU)RU\TPU\network\38644 | ||
035 | _aRU\TPU\network\35617 | ||
090 | _a667439 | ||
100 | _a20220324a2021 k y0engy50 ba | ||
101 | 0 | _aeng | |
102 | _aCH | ||
135 | _adrcn ---uucaa | ||
181 | 0 | _ai | |
182 | 0 | _ab | |
200 | 1 |
_aInnate Immunomodulatory Activity of Cedrol, a Component of Essential Oils Isolated from Juniperus Species _fG. Ozek, I. A. Shchepyotkin, M. Yermagambetova [et al.] |
|
203 |
_aText _celectronic |
||
300 | _aTitle screen | ||
320 | _a[References: 101 tit.] | ||
330 | _aLittle is known about the immunomodulatory activity of essential oils isolated from Juniperus species. Thus, we isolated essential oils from the cones and leaves of eight juniper species found in Montana and in Kazakhstan, including J. horizontalis, J. scopolorum, J. communis, J. seravschanica, J. sabina, J. pseudosabina, J. pseudosabina subsp. turkestanica, and J. sibirica. We report here the chemical composition and innate immunomodulatory activity of these essential oils. Compositional analysis of the 16 samples of Juniper essential oils revealed similarities and differences between our analyses and those previously reported for essential oils from this species. Our studies represent the first analysis of essential oils isolated from the cones of four of these Juniper species. Several essential oil samples contained high levels of cedrol, which was fairly unique to three Juniper species from Kazakhstan. We found that these essential oils and pure (+)-cedrol induced intracellular Ca2+ mobilization in human neutrophils. Furthermore, pretreatment of human neutrophils and N-formyl peptide receptor 1 and 2 (FPR1 and FPR2) transfected HL60 cells with these essential oils or (+)-cedrol inhibited agonist-induced Ca2+ mobilization, suggesting these responses were desensitized by this pretreatment. In support of this conclusion, pretreatment with essential oils from J. seravschanica cones (containing 16.8% cedrol) or pure (+)-cedrol inhibited human neutrophil chemotaxis to N-formyl peptide. Finally, reverse pharmacophore mapping predicted several potential kinase targets for cedrol. Thus, our studies have identified cedrol as a novel neutrophil agonist that can desensitize cells to subsequent stimulation by N-formyl peptide. | ||
461 | _tMolecules | ||
463 |
_tVol. 26, iss. 24 _v[7644, 20 p.] _d2021 |
||
610 | 1 | _aтруды учёных ТПУ | |
610 | 1 | _aэлектронный ресурс | |
610 | 1 | _ajuniperus | |
610 | 1 | _aessential oil | |
610 | 1 | _acalcium flux | |
610 | 1 | _aneutrophil | |
610 | 1 | _achemotaxis | |
610 | 1 | _asesquiterpene | |
610 | 1 | _acedrol | |
610 | 1 | _aэфирные масла | |
610 | 1 | _aнейтрофилы | |
610 | 1 | _aпротивовоспалительные свойства | |
610 | 1 | _aцедрол | |
610 | 1 | _aможжевельник | |
701 | 1 |
_aOzek _bG. _gGulmira |
|
701 | 1 |
_aShchepyotkin _bI. A. _gIgor Aleksandrovich |
|
701 | 1 |
_aYermagambetova _bM. _gMoldir |
|
701 | 1 |
_aOzek _bT. _gTemel |
|
701 | 1 |
_aKirpotina _bL. N. _gLiliya Nikolaevna |
|
701 | 1 |
_aAlmerekova _bSh. S. _gShyryn |
|
701 | 1 |
_aAbugalieva _bS. I. _gSaule |
|
701 | 1 |
_aKhlebnikov _bA. I. _cChemist _cProfessor of Tomsk Polytechnic University _f1963- _gAndrey Ivanovich _2stltpush _3(RuTPU)RU\TPU\pers\33927 |
|
701 | 1 |
_aQuinn _bM. T. _gMark |
|
712 | 0 | 2 |
_aНациональный исследовательский Томский политехнический университет _bИнженерная школа новых производственных технологий _bНаучно-образовательный центр Н. М. Кижнера _h7872 _2stltpush _3(RuTPU)RU\TPU\col\23556 |
801 | 2 |
_aRU _b63413507 _c20220324 _gRCR |
|
856 | 4 | 0 | _uhttps://doi.org/10.3390/molecules26247644 |
942 | _cCF |