2006
DOI: 10.1016/j.intimp.2005.07.018
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In vitro induction of nitric oxide by mouse peritoneal macrophages treated with human placental extract

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Cited by 37 publications
(25 citation statements)
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“…The extract also exhibits anti-microbial activity against commonly occurring pathological organisms [17], in vitro induction of NO by mouse peritoneal macrophages [18] along with enhancement of cell adhesion [19]. These findings emphasize the regulatory action exhibited by the placental extract.…”
Section: Introductionmentioning
confidence: 88%
“…The extract also exhibits anti-microbial activity against commonly occurring pathological organisms [17], in vitro induction of NO by mouse peritoneal macrophages [18] along with enhancement of cell adhesion [19]. These findings emphasize the regulatory action exhibited by the placental extract.…”
Section: Introductionmentioning
confidence: 88%
“…It promotes inflammatory mediation of repair mechanism and wound matrix development followed by remodeling. The extract has also shown to induce interferon- (IFN-) production by macrophages (Chakraborty et al, 2006). Anti-microbial property of the extract against a large number of pathological microorganisms related to prevention of secondary infections to wounds has also been demonstrated.…”
Section: Biochemical Characterization and Possible Mechanism Of Actiomentioning
confidence: 98%
“…The aqueous extract has been investigated in terms of induction of NO by macrophages. It has been demonstrated that with an increase of NO production, concomitant decrease in NADPH present in the applied placental extract was observed, thereby indicating that the NADPH pool of placental extract is metabolized, further justifying the biological potency of this nucleotide in the extract (Chakraborty et al, 2006). It has been well documented that nitric oxide (NO) has multiple effects at the molecular, cellular and physiological level in wound healing.…”
Section: Biochemical Characterization and Possible Mechanism Of Actiomentioning
confidence: 99%
“…К настоящему времени было предложе-но несколько различных молекулярных и физиологиче-ских механизмов, объясняющих ранозаживляющий эффект ГПЧ: увеличение уровней ростовых факторов фибробластов (ФРФ) [12], быстрая миграция нейтрофи-лов к ране [13], синтез NO, важнейшего клеточного меди-атора в заживлении ран [14]. В частности, в составе неко-торых препаратов на основе ГПЧ был найден противо-воспалительный дипептид JBP485 (цикло-транс-4-гидроксипролилсерин), который снижает уровни секре-ции и ФНО-альфа и проявляет антиапоптотический эффект (снижение уровней и активности каспазы-3 -фермента-активатора апоптоза клеток [15]).…”
Section: молекулярнофизиологические механизмы действия гпч на регенеunclassified