A probiotic mix partially protects against castration-induced bone loss in male mice.
Lina LaweniusHannah ColldénKarin L GustafssonJianyao WuLouise GrahnemoLiesbeth VandenputClaes OhlssonKlara SjögrenPublished in: The Journal of endocrinology (2022)
Studies in postmenopausal women and ovariectomized mice show that the probiotic mix Lacticaseibacillus paracasei DSM13434, Lactiplantibacillus plantarum DSM 15312 and DSM 15313 (L. Mix) can protect from bone loss caused by sex steroid deficiency. Whether probiotic bacteria can protect bone also in sex steroid-deficient males is less studied. We used the orchiectomized mouse as a model for age-dependent bone loss caused by decreasing sex hormone levels in males. We treated 10-week-old male mice with either vehicle (veh) or L. Mix for 6 weeks, starting 2 weeks before orchiectomy (orx) or sham surgery. Importantly, mice treated with L. Mix had a general increase in total body bone mineral density (BMD) and lean mass (P ≤ 0.05) compared with veh-treated mice. Detailed computer tomography analysis of dissected bones showed increased trabecular BMD of the distal metaphyseal region of the femur in L. Mix compared to veh-treated orx mice (+8.0%, P ≤ 0.05). In the vertebra, L. Mix treatment increased trabecular bone volume fraction BV/TV (+11.5%, P ≤ 0.05) compared to veh in orx mice. Also, L. Mix increased the levels of short-chain fatty acids (SCFAs) such as propionate and acetate and important intermediates in SCFA synthesis such as succinate and lactate in the cecal content of male mice. In conclusion, L. Mix treatment resulted in a general increase in BMD in adult male mice and prevented trabecular bone loss in femur and vertebra of orx mice. These bone protective effects of L. Mix were associated with increased levels of SCFAs in the cecal content of male mice.
Keyphrases
- bone mineral density
- bone loss
- postmenopausal women
- body composition
- high fat diet induced
- minimally invasive
- fatty acid
- insulin resistance
- coronary artery disease
- wild type
- young adults
- type diabetes
- clinical trial
- oxidative stress
- skeletal muscle
- randomized controlled trial
- machine learning
- acute coronary syndrome
- newly diagnosed
- inflammatory response
- lipopolysaccharide induced