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Study M039

Study name

Chen SL 2014

Title

Effect of Allium macrostemon on a rat model of depression studied by using plasma lipid and acylcarnitine profiles from liquid chromatography/mass spectrometry

Overall design

The present study aimed to investigate the anti-depressive effect of the traditional Chinese medicine Allium macrostemon (A.M.) in a rat model of depression induced by exposure to chronic immobilization stress. Lipid and acylcarnitine metabolism were set into the focus of this study due to their key role in the pathogenesis of depression. Plasma lipid profiling was performed by ultra fast liquid chromatography/ion trap-time of flight mass spectrometry. Ultra-high performance liquid chromatography/triple quadrupole mass spectrometry was used to characterize the plasma acylcarnitine profile. Rats were divided into 3 groups: (1) control group (n = 12), (2) CRS group (chronic immobilization stress, n = 12), and (3) CRS + A.M. group (chronic immobilization stress plus A.M. treatment at the dose of 10 mL/kg, n = 11). Rat in the CRS group or CRS + A.M. group was kept in a restraint box for 6 h every day, and the animal experiments lasted for 6 weeks. A.M. was administered once per day by intragastric during the model building period.

Study Type

Type1;

Type2;

Data available

Unavailable

Organism

Rat; Wistar rat;

Categories of depression

Animal model; Chronic restraint stress model; Chronic restraint stress model;

Criteria for depression

Tail suspension test

Sample size

35

Tissue

Peripheral; Blood; Plasma;

Platform

MS-based; LC-MS: Ultra fast liquid chromatography system coupled with ion trap time-of-flight mass spectrometry (UFLC/IT-TOF MS, Shimadzu, Kyoto, Japan);

MS-based; LC-MS: ultra-high performance liquid chromatography system coupled with triple quadrupole mass spectrometry (LC/MS QQQ 6460, Agilent, Santa Clara, CA, USA);

PMID

24284228

DOI

10.1016/j.jpba.2013.10.045

Citation

Chen S, Wei C, Gao P, et al. Effect of Allium macrostemon on a rat model of depression studied by using plasma lipid and acylcarnitine profiles from liquid chromatography/mass spectrometry. J Pharm Biomed Anal 2014;89:122-9.

Metabolite

LysoPC(18:1);

LysoPC(18:2);

LysoPC(20:1);

LysoPC(O-16:2);

LysoPC(O-18:3);

Carnitine C10:1;

Carnitine C12:0;

Carnitine C14:2;

Carnitine C14:1;

Carnitine C14:0;

Carnitine C16:2;

Carnitine C16:1;

Carnitine C16:0;

Linoelaidylcarnitine;

Oleoylcarnitine;

Stearoylcarnitine;

Carnitine C20:2;

Carnitine C20:1;

Carnitine C20:0;

Carnitine C14:0-OH;

Carnitine C16:1-OH;

Carnitine C16:0-OH;

Carnitine C18:2-OH;

Carnitine C18:1-OH;

PC(32:1);

PC(36:4);

PC(36:5);

PC(37:4);

PC(38:4);

PC(38:5);

PC(38:6);

PC(40:6);

PC(O-36:4);

PC(O-38:5);

TG(58:12);

TG(60:12);

TG(62:13);

TG(62:14);