Intravenous lipid emulsion therapy for acute clomipramine intoxication in rats

Abstract

AimIn this study, to assess the utility of lipid emulsion (ILE) therapy as a treatment option for overdoses of lipophilic drugs, we examined the detoxification effect of ILE therapy in rats that were administered overdoses of the tricyclic antidepressant clomipramine hydrochloride (CMI).MethodsFemale Wistar rats were orally administered 50 mg/kg CMI five times in 2‐h intervals to examine whether intralipos accelerated the elimination of CMI in the peripheral blood. Rats were divided into the intralipos (i.v. 2 g/kg intralipos) and placebo (i.v. saline) groups. The concentrations of CMI and desmethylclomipramine (DMCMI), a metabolite of CMI, in blood were measured over time by high‐performance liquid chromatography. We then gave the animals 100 mg/kg CMI orally to examine whether intralipos could inhibit the distribution of CMI. The CMI and DMCMI concentrations in peripheral blood, liver, and brain were measured 60 min after intralipos administration.ResultsThe blood concentration of CMI was significantly higher in the intralipos group than in the placebo group at 60 and 120 min. After a single administration of 100 mg/kg CMI, the ratio of the concentration of CMI in liver/serum was significantly lower in the intralipos group than in the placebo group. We also found a significantly faster elimination rate for CMI in peripheral blood in the intralipos group than in the placebo group.ConclusionThe distribution of CMI from blood to tissue was suppressed by intralipos. Therefore, ILE therapy is a promising candidate for the treatment of overdoses of lipophilic drugs.

Stomach secretes estrogen in response to the blood triglyceride levels

“…To increase the blood triglyceride levels without the effects of ingested fatty acids on the gastrointestinal tract, soy oil emulsion (2 mL of 20% soy oil emulsion per kg body weight) or control saline was injected into rat tail vein (Fig. 4a ) 35 , 36 . Tail venous triglyceride and E2 levels were measured before (0 h) and at 0.1, 0.5, 1, 1.5, 2, 3, 4, and 5 h after the injection.…”