BACKGROUND
Previous studies have shown that Lactobacillus plantarum LIP‐1 (hereafter LIP‐1) has an obvious hypolipidemic effect, and microencapsulated probiotics can ensure the strains live through the gastrointestinal tract. Although there has been much research on both preparation and assessment methods for probiotics microcapsules, most assessments were made in vitro and few were validated in vivo. In this study, the protective effect of microencapsulation and the possible hypolipidemic mechanisms of probiotic LIP‐1 were evaluated in rats. Treatments included rats fed on a normal diet, a high‐fat diet, and a high‐fat diet with an intragastric supplement of either non‐microencapsulated LIP‐1 cells (NME LIP‐1) or microencapsulated LIP‐1 (ME LIP‐1). Lipid metabolism indicators were measured during the experiment and following euthanasia.
RESULTS
Microencapsulation increased survival and colonization of LIP‐1 in the colon. ME LIP‐1 was superior to NME LIP‐1 in reducing cholesterol. The mechanisms behind the hypolipidemic effect exerted by LIP‐1 are possibly due to promoting the excretion of cholesterol, improving antioxygenic potentials, enhancing recovery from the injury in the liver, cardiovascular intima and intestinal mucosa, promoting the generation of short‐chain fatty acids, and improving lipid metabolism.
CONCLUSIONS
This study confirms that microencapsulation provides effective protection of LIP‐1 in the digestive system and the role of LIP‐1 in the prevention and cure of hyperlipidaemia, providing theoretical support for probiotics to enter clinical applications. © 2019 Society of Chemical Industry