Nicotinamide mononucleotide reduces metabolic-syndrome-associated lens stiffening and gut microbiota–metabolic–ocular changes in mice

Introduction Lens stiffening contributes to impaired accommodation and age-related optical dysfunction, but whether metabolic syndrome (MetS) accelerates this biomechanical change in association with microbiota-linked metabolic disturbances remains unclear. This study evaluated whether nicotinamide mononucleotide (NMN) reduces lens stiffening in mice with diet-induced metabolic syndrome and whether changes in gut microbial metabolites, systemic inflammatory markers, and ocular biochemical injury accompany this response. Methods Male and female C57BL/6J mice were fed a high-fat/high-sucrose regimen and assigned to vehicle, NMN dose, antibiotic-depletion, NMN plus antibiotic-depletion, and fecal microbiota transfer arms. A total of 96 mice were randomized, and 94 mice contributed valid week-16 lens stiffness measurements. The primary endpoint was lens apparent Young’s modulus. Secondary endpoints included Homeostatic Model Assessment of Insulin Resistance (HOMA-IR), serum triglyceride, fecal microbiota diversity, fecal short-chain fatty acids, serum lipopolysaccharide (LPS) and trimethylamine N-oxide (TMAO), lens nicotinamide adenine dinucleotide (NAD+), oxidative and glycation-related injury, and molecular fibrosis-associated lens markers. Results Compared with controls, metabolic-syndrome mice showed higher HOMA-IR, serum triglyceride, serum LPS, serum TMAO, lens malondialdehyde (MDA), lens advanced glycation end-products (AGEs), and lens apparent Young’s modulus, with lower fecal butyrate and lens NAD+. Lens apparent Young’s modulus increased from 7.4 ± 1.3 kPa in controls to 17.9 ± 2.1 kPa in metabolic-syndrome mice. NMN reduced lens stiffness to 14.8 ± 2.0 kPa at 150 mg/kg/day and 11.9 ± 2.4 kPa at 300 mg/kg/day. Fecal butyrate increased from 8.1 ± 1.9 μmol/g in metabolic-syndrome mice to 12.0 ± 2.4 μmol/g and 13.7 ± 2.8 μmol/g in the two NMN groups, while lens NAD+ increased from 1.50 ± 0.28 to 1.96 ± 0.31 pmol/mg and 2.34 ± 0.35 pmol/mg, respectively. Antibiotic depletion weakened but did not abolish the high-dose NMN ocular response, and fecal transfer from NMN-treated donors partially shifted microbial metabolite and lens stiffness endpoints toward the direct NMN-treatment profile. Discussion These findings support an NMN-associated reduction in metabolic-syndrome-related lens stiffening accompanied by coordinated systemic metabolic, microbial-metabolite, and ocular biochemical changes; the microbiota-related component appeared contributory rather than sufficient to explain the ocular response.

Authors

Institutions

Publication Details

Journal
Frontiers in Microbiology
Published
2026-11-02
DOI
https://doi.org/10.3389/fmicb.2026.1939489
Primary Topic
Sirtuins and Resveratrol in Medicine
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Nicotinamide mononucleotide reduces metabolic-syndrome-associated lens stiffening and gut microbiota–metabolic–ocular changes in mice

Wanying Song, 冯启廷, Lai Wei, Quan Liu
2 links
Frontiers in Microbiology
Sirtuins and Resveratrol in Medicine
article

Nicotinamide mononucleotide reduces metabolic-syndrome-associated lens stiffening and gut microbiota–metabolic–ocular changes in mice

Wanying Song, 冯启廷, Lai Wei, Quan Liu
article en

Abstract

Introduction Lens stiffening contributes to impaired accommodation and age-related optical dysfunction, but whether metabolic syndrome (MetS) accelerates this biomechanical change in association with microbiota-linked metabolic disturbances remains unclear. This study evaluated whether nicotinamide mononucleotide (NMN) reduces lens stiffening in mice with diet-induced metabolic syndrome and whether changes in gut microbial metabolites, systemic inflammatory markers, and ocular biochemical injury accompany this response. Methods Male and female C57BL/6J mice were fed a high-fat/high-sucrose regimen and assigned to vehicle, NMN dose, antibiotic-depletion, NMN plus antibiotic-depletion, and fecal microbiota transfer arms. A total of 96 mice were randomized, and 94 mice contributed valid week-16 lens stiffness measurements. The primary endpoint was lens apparent Young’s modulus. Secondary endpoints included Homeostatic Model Assessment of Insulin Resistance (HOMA-IR), serum triglyceride, fecal microbiota diversity, fecal short-chain fatty acids, serum lipopolysaccharide (LPS) and trimethylamine N-oxide (TMAO), lens nicotinamide adenine dinucleotide (NAD+), oxidative and glycation-related injury, and molecular fibrosis-associated lens markers. Results Compared with controls, metabolic-syndrome mice showed higher HOMA-IR, serum triglyceride, serum LPS, serum TMAO, lens malondialdehyde (MDA), lens advanced glycation end-products (AGEs), and lens apparent Young’s modulus, with lower fecal butyrate and lens NAD+. Lens apparent Young’s modulus increased from 7.4 ± 1.3 kPa in controls to 17.9 ± 2.1 kPa in metabolic-syndrome mice. NMN reduced lens stiffness to 14.8 ± 2.0 kPa at 150 mg/kg/day and 11.9 ± 2.4 kPa at 300 mg/kg/day. Fecal butyrate increased from 8.1 ± 1.9 μmol/g in metabolic-syndrome mice to 12.0 ± 2.4 μmol/g and 13.7 ± 2.8 μmol/g in the two NMN groups, while lens NAD+ increased from 1.50 ± 0.28 to 1.96 ± 0.31 pmol/mg and 2.34 ± 0.35 pmol/mg, respectively. Antibiotic depletion weakened but did not abolish the high-dose NMN ocular response, and fecal transfer from NMN-treated donors partially shifted microbial metabolite and lens stiffness endpoints toward the direct NMN-treatment profile. Discussion These findings support an NMN-associated reduction in metabolic-syndrome-related lens stiffening accompanied by coordinated systemic metabolic, microbial-metabolite, and ocular biochemical changes; the microbiota-related component appeared contributory rather than sufficient to explain the ocular response.

Frontiers in MicrobiologyVol. 17
Second Affiliated Hospital of Guangzhou Medical University (CN), State Key Laboratory of Ophthalmology (CN), Zhongshan Ophthalmic Center, Sun Yat-sen University (CN), Guangzhou Medical University (CN)
Good health and well-being
Openalex Percentile: Top 17%
Sirtuins and Resveratrol in Medicine
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Laika access coming soon