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035 _a(RuTPU)RU\TPU\network\17609
035 _aRU\TPU\network\17576
090 _a652325
100 _a20161219a2016 k y0engy50 ba
101 1 _aeng
_deng
102 _aUS
135 _adrcn ---uucaa
181 0 _ai
182 0 _ab
200 1 _aModulation of Human Neutrophil Responses by the Essential Oils from Ferula akitschkensis and Their Constituents
_fI. A. Schepetkin, S. V. Kushnarenko, G. Ozek [et al.]
203 _aText
_celectronic
300 _aTitle screen
330 _aEssential oils were obtained by hydrodistillation of the umbels+seeds and stems of Ferula akitschkensis (FAEOu/s and FAEOstm, respectively) and analyzed by gas chromatography and gas chromatography-mass spectrometry. Fifty-two compounds were identified in FAEOu/s; the primary components were sabinene, α-pinene, β-pinene, terpinen-4-ol, eremophilene, and 2-himachalen-7-ol, whereas the primary components of FAEOstm were myristicin and geranylacetone. FAEOu/s, β-pinene, sabinene, γ-terpinene, geranylacetone, isobornyl acetate, and (E)-2-nonenal stimulated [Ca2+]i mobilization in human neutrophils, with the most potent being geranylacetone (EC50 = 7.6 ± 1.9 μM) and isobornyl acetate 6.4 ± 1.7 (EC50 = 7.6 ± 1.9 μM). In addition, treatment of neutrophils with β-pinene, sabinene, γ-terpinene, geranylacetone, and isobornyl acetate desensitized the cells to N-formyl-Met-Leu-Phe (fMLF)- and interleukin-8 (IL-8)-induced [Ca2+]i flux and inhibited fMLF-induced chemotaxis. The effects of β-pinene, sabinene, γ-terpinene, geranylacetone, and isobornyl acetate on neutrophil [Ca2+]i flux were inhibited by transient receptor potential (TRP) channel blockers.
333 _aРежим доступа: по договору с организацией-держателем ресурса
461 _tJournal of Agricultural and Food Chemistry
_d1953-
463 _tVol. 64, № 38
_v[P. 7156–7170]
_d2016
610 1 _aэлектронный ресурс
610 1 _aтруды учёных ТПУ
610 1 _aэфирные масла
610 1 _aчеловеческий организм
610 1 _aреакции
701 1 _aSchepetkin (Shchepyotkin)
_bI. A.
_cdoctor-biophysicist
_cleading researcher of Tomsk Polytechnic University, candidate of medical science
_f1962-
_gIgor Aleksandrovich
_2stltpush
_3(RuTPU)RU\TPU\pers\37358
701 1 _aKushnarenko
_bS. V.
_gSvetlana
701 1 _aOzek
_bG.
_gGulmira
701 1 _aKirpotina
_bL. N.
_gLiliya Nikolaevna
701 1 _aSinharoy
_bP.
_gPritam
701 1 _aUtegenova
_bG. A.
_gGulzhakhan
701 1 _aAbidkulova
_bK. T.
_gKarime
701 1 _aOzek
_bT.
_gTemel
701 1 _aBaser
_bK. H. C.
_gKemal Husnu Can
701 1 _aKovrizhina
_bA. R.
_cbiotechnology specialist
_cResearch Engineer of Tomsk Polytechnic University
_f1995-
_gAnastasia Ruslanovna
_2stltpush
_3(RuTPU)RU\TPU\pers\46608
701 1 _aKhlebnikov
_bA. I.
_cChemist
_cProfessor of Tomsk Polytechnic University
_f1963-
_gAndrey Ivanovich
_2stltpush
_3(RuTPU)RU\TPU\pers\33927
701 1 _aDamron
_bD. S.
_gDerek
701 1 _aQuinn
_bM. T.
_gMark
712 0 2 _aНациональный исследовательский Томский политехнический университет (ТПУ)
_bИнститут физики высоких технологий (ИФВТ)
_bКафедра биотехнологии и органической химии (БИОХ)
_h6810
_2stltpush
_3(RuTPU)RU\TPU\col\18693
801 2 _aRU
_b63413507
_c20201103
_gRCR
856 4 _uhttp://dx.doi.org/10.1021/acs.jafc.6b03205
942 _cCF