Stranik Jaroslav, Kacerovsky Marian, Sterba Martin, Andrys Ctirad, Abad Cilia, Staud Frantisek, Micuda Stanislav, Soucek Ondrej, Jacobsson Bo, Musilova Ivana
Department of Obstetrics and Gynecology, University Hospital Hradec Kralove, Faculty of Medicine in Hradec Kralove, Charles University, Hradec Kralove, Czechia.
Biomedical Research Center, University Hospital Hradec Kralove, Hradec Kralove, Czechia.
Front Pharmacol. 2022 Apr 12;13:871193. doi: 10.3389/fphar.2022.871193. eCollection 2022.
To develop a rat model of intra-amniotic inflammation, characterized by the concentration of interleukin-6 in the amniotic fluid, induced by an ultrasound-guided transabdominal administration of lipopolysaccharide into individual gestational sacs. An ultrasound-guided transabdominal intra-amniotic administration of lipopolysaccharide or phosphate-buffered saline (PBS) as control was performed in rats on embryonic day 18. Only accessible gestational sacs with precise recording of their positions were injected. Twenty-four hours later, individual amniotic fluid samples were collected from the gestational sacs of laparotomized animals. The gestational sacs were divided into four subgroups: (i) with lipopolysaccharide: injected gestational sacs from rats undergoing lipopolysaccharide administration; (ii) without lipopolysaccharide: non-injected gestational sacs from rats undergoing lipopolysaccharide administration; (iii) with PBS: injected gestational sacs from rats undergoing PBS administration; and (iv) without PBS: non-injected gestational sacs from rats undergoing PBS administration. The concentration of interleukin-6 in individual amniotic fluid samples was assessed using ELISA. In the group of five animals receiving lipopolysaccharide, 24 (33%) and 48 (77%) gestational sacs were and were not injected, respectively. The amniotic fluid was obtained from 21 (88%) injected and 46 (95%) non-injected sacs. In the control group of five animals receiving phosphate-buffered saline, 28 (35%) and 52 (75%) gestational sacs were and were not injected, respectively. The amniotic fluid was obtained from 18 (64%) injected and 50 (96%) non-injected sacs. No labor occurred, and only one fetal death was observed in a gestational sac injected with lipopolysaccharide. Differences in concentrations of interleukin-6 in the amniotic fluid were found among the subgroups of the gestational sacs (with lipopolysaccharide: median 762 pg/ml; without lipopolysaccharide: median 35.6 pg/ml; with PBS: median 35.6 pg/ml; and without PBS: median 35.6 pg/ml; < 0.0001). Concentrations of interleukin-6 in the amniotic fluid from the gestational sacs with lipopolysaccharide were significantly higher than those in the three remaining subgroups ( < 0.0001). No differences in concentrations of interleukin-6 in the amniotic fluid were identified between the three remaining subgroups. The ultrasound-guided transabdominal intra-amniotic administration of lipopolysaccharide with a subsequent collection and analysis of amniotic fluid samples is feasible in rats. The intra-amniotic administration of lipopolysaccharide led to the development of intra-amniotic inflammation without leading to fetal mortality or induction of labor.
为建立羊膜内炎症大鼠模型,该模型以羊水中白细胞介素-6的浓度为特征,通过超声引导经腹向单个妊娠囊内注射脂多糖来诱导。在胚胎第18天对大鼠进行超声引导经腹羊膜内注射脂多糖或作为对照的磷酸盐缓冲盐水(PBS)。仅对可触及的妊娠囊进行注射,并精确记录其位置。24小时后,从剖腹动物的妊娠囊中收集单个羊水样本。妊娠囊分为四个亚组:(i)脂多糖组:接受脂多糖注射的大鼠的注射妊娠囊;(ii)无脂多糖组:接受脂多糖注射的大鼠的未注射妊娠囊;(iii)PBS组:接受PBS注射的大鼠的注射妊娠囊;(iv)无PBS组:接受PBS注射的大鼠的未注射妊娠囊。使用酶联免疫吸附测定法(ELISA)评估单个羊水样本中白细胞介素-6的浓度。在接受脂多糖的五只动物组中,分别有24个(33%)和48个(77%)妊娠囊被注射和未被注射。从21个(88%)注射妊娠囊和46个(95%)未注射妊娠囊中获取了羊水。在接受磷酸盐缓冲盐水的五只动物对照组中,分别有28个(35%)和52个(75%)妊娠囊被注射和未被注射。从18个(64%)注射妊娠囊和50个(96%)未注射妊娠囊中获取了羊水。未发生分娩,仅在一个注射脂多糖的妊娠囊中观察到一例胎儿死亡。在妊娠囊亚组之间发现羊水白细胞介素-6浓度存在差异(脂多糖组:中位数762 pg/ml;无脂多糖组:中位数35.6 pg/ml;PBS组:中位数35.6 pg/ml;无PBS组:中位数35.6 pg/ml;<0.0001)。脂多糖组妊娠囊羊水白细胞介素-6浓度显著高于其余三个亚组(<0.0001)。其余三个亚组之间未发现羊水白细胞介素-6浓度存在差异。超声引导经腹羊膜内注射脂多糖并随后收集和分析羊水样本在大鼠中是可行的。羊膜内注射脂多糖导致羊膜内炎症的发生,但未导致胎儿死亡或引产。