Lactobacillus and Bifidobacterium Improves Physiological Function and Cognitive Ability in Aged Mice by the Regulation of Gut Microbiota

Oxidative stress, aging, and diseases

Liguori, I., Russo, G., Curcio, F., Bulli, G., Aran, L., Della-Morte, D., Gargiulo, G., Testa, G., Cacciatore, F., Bonaduce, D., et al. (2018) · Clinical Interventions in Aging · doi:10.2147/cia.s158513 · Cited by 3,979 · see citing works

Inflammaging: a new immune–metabolic viewpoint for age-related diseases

Franceschi, C., Garagnani, P., Parini, P., Giuliani, C., & Santoro, A. (2018) · Nature Reviews Endocrinology · doi:10.1038/s41574-018-0059-4 · Cited by 3,586 · see citing works

Gut microbiota composition correlates with diet and health in the elderly

Claesson, M. J., Jeffery, I. B., Conde, S., Power, S. E., O’Connor, E. M., Cusack, S., Harris, H. M. B., Coakley, M., Lakshminarayanan, B., O’Sullivan, O., et al. (2012) · Nature · doi:10.1038/nature11319 · Cited by 3,314 · see citing works

Understanding the odd science of aging

Kirkwood, T. B. L. (2005) · Cell · doi:10.1016/j.cell.2005.01.027 · Cited by 1,984 · see citing works

The gut microbiome in health and in disease

Shreiner, A. B., Kao, J. Y., & Young, V. B. (2014) · Current Opinion in Gastroenterology · doi:10.1097/mog.0000000000000139 · Cited by 1,695 · see citing works

Object recognition test in mice

Leger, M., Quiedeville, A., Bouet, V., Haelewyn, B., Boulouard, M., Schumann-Bard, P., & Freret, T. (2013) · Nature Protocols · doi:10.1038/nprot.2013.155 · Cited by 1,357 · see citing works

Gut microbiota and aging

O’Toole, P. W., & Jeffery, I. B. (2015) · Science · doi:10.1126/science.aac8469 · Cited by 1,202 · see citing works

Cellular senescence drives age-dependent hepatic steatosis

Ogrodnik, M., Miwa, S., Tchkonia, T., Tiniakos, D., Wilson, C. L., Lahat, A., Day, C. P., Burt, A., Palmer, A., Anstee, Q. M., et al. (2017) · Nature Communications · doi:10.1038/ncomms15691 · Cited by 1,044 · see citing works

Effect of Probiotic Supplementation on Cognitive Function and Metabolic Status in Alzheimer's Disease: A Randomized, Double-Blind and Controlled Trial

Akbari, E., Asemi, Z., Daneshvar Kakhaki, R., Bahmani, F., Kouchaki, E., Tamtaji, O. R., Hamidi, G. A., & Salami, M. (2016) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2016.00256 · Cited by 946 · see citing works

Probiotics and antibodies to TNF inhibit inflammatory activity and improve nonalcoholic fatty liver disease

Li, Z., Yang, S., Lin, H., Huang, J., Watkins, P. A., Moser, A. B., Desimone, C., Song, X.-Y., & Diehl, A. M. (2003) · Hepatology · doi:10.1053/jhep.2003.50048 · Cited by 930 · see citing works

Skeletal muscle performance and ageing

Tieland, M., Trouwborst, I., & Clark, B. C. (2018) · Journal of Cachexia, Sarcopenia and Muscle · doi:10.1002/jcsm.12238 · Cited by 904 · see citing works

Consequences of Age-Related Cognitive Declines

Salthouse, T. (2012) · Annual Review of Psychology · doi:10.1146/annurev-psych-120710-100328 · Cited by 818 · see citing works

Gut Bifidobacteria Populations in Human Health and Aging

Arboleya, S., Watkins, C., Stanton, C., & Ross, R. P. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.01204 · Cited by 683 · see citing works

Gut microbiome and aging: physiological and mechanistic insights

Nagpal, R., Mainali, R., Ahmadi, S., Wang, S., Singh, R., Kavanagh, K., Kitzman, D. W., Kushugulova, A., Marotta, F., & Yadav, H. (2018) · Nutrition and Healthy Aging · doi:10.3233/nha-170030 · Cited by 670 · see citing works

Antioxidative Ability of Lactic Acid Bacteria

Lin, M., & Yen, C.-L. (1999) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf981149l · Cited by 511 · see citing works

Can probiotics modulate human disease by impacting intestinal barrier function?

Bron, P. A., Kleerebezem, M., Brummer, R.-J., Cani, P. D., Mercenier, A., MacDonald, T. T., Garcia-Ródenas, C. L., & Wells, J. M. (2017) · British Journal Of Nutrition · doi:10.1017/s0007114516004037 · Cited by 499 · see citing works

Probiotics, their health benefits and applications for developing healthier foods: a review

Nagpal, R., Kumar, A., Kumar, M., Behare, P. V., Jain, S., & Yadav, H. (2012) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.2012.02593.x · Cited by 496 · see citing works

The role of the hippocampus in flexible cognition and social behavior

Rubin, R. D., Watson, P. D., Duff, M. C., & Cohen, N. J. (2014) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2014.00742 · Cited by 489 · see citing works

Probiotics as Potential Antioxidants: A Systematic Review

Mishra, V., Shah, C., Mokashe, N. U., Chavan, R. S., Yadav, H., & Prajapati, J. B. (2015) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf506326t · Cited by 462 · see citing works

Gut Microbiota Contribute to Age-Related Changes in Skeletal Muscle Size, Composition, and Function: Biological Basis for a Gut-Muscle Axis

Grosicki, G. J., Fielding, R. A., & Lustgarten, M. S. (2018) · Calcified Tissue International · doi:10.1007/s00223-017-0345-5 · Cited by 388 · see citing works

Small metabolites, possible big changes: A microbiota-centered view of non-alcoholic fatty liver disease

Chu, H., Duan, Y., Yang, L., & Schnabl, B. (2019) · Gut · doi:10.1136/gutjnl-2018-316307 · Cited by 354 · see citing works

Lactobacillus plantarum TWK10 Supplementation Improves Exercise Performance and Increases Muscle Mass in Mice

Chen, Y.-M., Wei, L., Chiu, Y.-S., Hsu, Y.-J., Tsai, T.-Y., Wang, M.-F., & Huang, C.-C. (2016) · Nutrients · doi:10.3390/nu8040205 · Cited by 297 · see citing works

Restoring Specific Lactobacilli Levels Decreases Inflammation and Muscle Atrophy Markers in an Acute Leukemia Mouse Model

Bindels, L. B., Beck, R., Schakman, O., Martin, J. C., De Backer, F., Sohet, F. M., Dewulf, E. M., Pachikian, B. D., Neyrinck, A. M., Thissen, J.-P., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0037971 · Cited by 278 · see citing works

Age-associated Impairment of the Mucus Barrier Function is Associated with Profound Changes in Microbiota and Immunity

Sovran, B., Hugenholtz, F., Elderman, M. E., van Beek, A. A., Graversen, K., Huijskes, M., Boekschoten, M. V., Savelkoul, H. F. J., de Vos, P., Dekker, J. P., et al. (2019) · Scientific Reports · doi:10.1038/s41598-018-35228-3 · Cited by 237 · see citing works

Neurotrophic factors in Alzheimer's and Parkinson's diseases: implications for pathogenesis and therapy

Pinton, S., Sampaio, T. B., Savall, A. S. P., & Gutierrez, M. Z. (2017) · Neural Regeneration Research · doi:10.4103/1673-5374.205084 · Cited by 219 · see citing works

Oral administration of dahi containing probioticLactobacillus acidophilusandLactobacillus caseidelayed the progression of streptozotocin-induced diabetes in rats

Yadav, H., Jain, S., & Sinha, P. R. (2008) · Journal of Dairy Research · doi:10.1017/s0022029908003129 · Cited by 211 · see citing works

Age-dependent changes in GI physiology and microbiota: time to reconsider?

An, R., Wilms, E., Masclee, A. A. M., Smidt, H., Zoetendal, E. G., & Jonkers, D. (2018) · Gut · doi:10.1136/gutjnl-2017-315542 · Cited by 209 · see citing works

Aging and the human gut microbiota—from correlation to causality

Saraswati, S., & Sitaraman, R. (2015) · Frontiers in Microbiology · doi:10.3389/fmicb.2014.00764 · Cited by 153 · see citing works

Lactobacillus casei DN-114 001 inhibits the increase in paracellular permeability of enteropathogenic Escherichia coli-infected T84 cells

Parassol, N., Freitas, M., Thoreux, K., Dalmasso, G., Bourdet‐Sicard, R., & Rampal, P. (2004) · Research in Microbiology · doi:10.1016/j.resmic.2004.09.013 · Cited by 146 · see citing works

Lactobacillus casei Shirota protects from fructose-induced liver steatosis: A mouse model

Wagnerberger, S., Spruss, A., Kanuri, G., Stahl, C., Schröder, M., Vetter, W., Bischoff, S. C., & Bergheim, I. (2012) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2012.01.014 · Cited by 123 · see citing works

The impact of ageing on the intestinal epithelial barrier and immune system

Man, A., Gicheva, N., & Nicoletti, C. (2014) · Cellular Immunology · doi:10.1016/j.cellimm.2014.04.001 · Cited by 114 · see citing works

Bifidobacterium longum supplementation improved high-fat-fed-induced metabolic syndrome and promoted intestinal Reg I gene expression

Chen, J. J., Wang, R., Li, X., & Wang, R. (2011) · Experimental Biology and Medicine · doi:10.1258/ebm.2011.010399 · Cited by 112 · see citing works

Lactobacillus sakei Alleviates High‐Fat‐Diet‐Induced Obesity and Anxiety in Mice by Inducing AMPK Activation and SIRT1 Expression and Inhibiting Gut Microbiota‐Mediated NF‐κB Activation

Jang, H., Han, S., Kim, J., Oh, S., Jang, H., & Kim, D. (2019) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201800978 · Cited by 112 · see citing works

Lactobacillus plantarum LC27 and Bifidobacterium longum LC67 simultaneously alleviate high-fat diet-induced colitis, endotoxemia, liver steatosis, and obesity in mice

In Kim, H., Kim, J.-K., Kim, J.-Y., Jang, S.-E., Han, M. J., & Kim, D.-H. (2019) · Nutrition Research · doi:10.1016/j.nutres.2019.03.008 · Cited by 82 · see citing works

Probiotic Bacteria for Healthier Aging: Immunomodulation and Metabolism of Phytoestrogens

Landete, J. M., Gaya, P., Rodríguez, E., Langa, S., Peirotén, Á., Medina, M., & Arqués, J. L. (2017) · BioMed Research International · doi:10.1155/2017/5939818 · Cited by 76 · see citing works

Understanding mode of action can drive the translational pipeline towards more reliable health benefits for probiotics

Kleerebezem, M., Binda, S., Bron, P. A., Gross, G., Hill, C., Vlieg, J. E. V. H., Lebeer, S., Satokari, R. M., & Ouwehand, A. C. (2018) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2018.09.007 · Cited by 73 · see citing works

The effects of ageing on the colonic bacterial microflora in adults

Enck, P., Zimmermann, K., Rusch, K., Schwiertz, A., Klosterhalfen, S., & Frick, J.-S. (2009) · Zeitschrift für Gastroenterologie · doi:10.1055/s-0028-1109055 · Cited by 68 · see citing works

Novel strategies for anti-aging drug discovery

Saraswat, K., & Rizvi, S. I. (2017) · Expert Opinion on Drug Discovery · doi:10.1080/17460441.2017.1349750 · Cited by 66 · see citing works

Endotoxin-induced skeletal muscle wasting is prevented by angiotensin-(1–7) through a p38 MAPK-dependent mechanism

Morales, M. G., Olguín, H., Di Capua, G., Brandan, E., Simon, F., & Cabello-Verrugio, C. (2015) · Clinical Science · doi:10.1042/cs20140840 · Cited by 62 · see citing works

Pilose antler polypeptides ameliorate inflammation and oxidative stress and improves gut microbiota in hypoxic-ischemic injured rats

Ni, Y., Wang, Z., Ma, L., Yang, L., Wu, T., & Fu, Z. (2019) · Nutrition Research · doi:10.1016/j.nutres.2019.01.005 · Cited by 53 · see citing works

Protective effects of astaxanthin on a combination of D-galactose and jet lag-induced aging model in mice

Ni, Y., Wu, T., Yang, L., Xu, Y., Ota, T., & Fu, Z. (2018) · Endocrine Journal · doi:10.1507/endocrj.ej17-0500 · Cited by 32 · see citing works

Maternal exposure to imazalil disrupts the endocrine system in F1 generation mice

Jin, C., Zhang, R., Fu, Z., & Jin, Y. (2019) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2019.03.002 · Cited by 32 · see citing works

Brain-derived Neurotrophic Factor Is Associated with Cognitive Impairment in Elderly Korean Individuals

Lee, S. J., Baek, J.-H., & Kim, Y.-H. (2015) · Clinical Psychopharmacology and Neuroscience · doi:10.9758/cpn.2015.13.3.283 · Cited by 30 · see citing works

Pilose antler polypeptides ameliorates hypoxic-ischemic encephalopathy by activated neurotrophic factors and SDF1/CXCR4 axis in rats

Wu, T., Yang, L., Chen, Y., Ni, Y., Jiang, J., Zhang, W., Zhou, Q., Zheng, X., Wang, Q., Fu, Z., et al. (2018) · Acta Biochimica et Biophysica Sinica · doi:10.1093/abbs/gmy005 · Cited by 20 · see citing works

Neurosteroid dehydroepiandrosterone improves active avoidance retrieval and induces antidepressant-like behavior in rats

Samardžić, J., Henčić, B., Jančić, J., Jadzic, D., Djuric, M., Obradovic, D. I., & Štrac, D. Š. (2017) · Neuroscience Letters · doi:10.1016/j.neulet.2017.09.013 · Cited by 13 · see citing works

The involvement of sympathetic nervous system in essence of chicken-facilitated physiological adaption and circadian resetting

Ni, Y., Ma, L., Wu, T., Lim, A. L., Zhang, W., Yang, L., Nakao, Y., & Fu, Z. (2018) · Life Sciences · doi:10.1016/j.lfs.2018.03.047 · Cited by 9 · see citing works

Spermidine improves gut barrier integrity and gut microbiota function in diet-induced obese mice

Ma, L., Ni, Y., Wang, Z., Tu, W., Ni, L., Zhuge, F., Zheng, A., Hu, L., Zhao, Y., Zheng, L., et al. (2020) · Gut Microbes · doi:10.1080/19490976.2020.1832857 · Cited by 596 · see citing works

Diet and the Microbiota–Gut–Brain Axis: Sowing the Seeds of Good Mental Health

Berding, K., Vlckova, K., Marx, W., Schellekens, H., Stanton, C., Clarke, G., Jacka, F., Dinan, T. G., & Cryan, J. F. (2021) · Advances in Nutrition · doi:10.1093/advances/nmaa181 · Cited by 451 · see citing works

Nutritional Components in Western Diet Versus Mediterranean Diet at the Gut Microbiota–Immune System Interplay. Implications for Health and Disease

Montero, C. G., Fraile‐Μartinez, O., Gomez-Lahoz, A. M., Pekarek, L., Castellanos, A. J., Noguerales-Fraguas, F., Coca, S., Guijarro, L. G., García‐Honduvilla, N., Asúnsolo, Á., et al. (2021) · Nutrients · doi:10.3390/nu13020699 · Cited by 452 · see citing works

Understanding the gut microbiota and sarcopenia: a systematic review

Liu, C., Cheung, W., Li, J., Chow, S. K., Yu, J., Wong, S. H., Ip, M., Sung, J. J. Y., & Wong, R. M. Y. (2021) · Journal of Cachexia, Sarcopenia and Muscle · doi:10.1002/jcsm.12784 · Cited by 363 · see citing works

Gut microbiota and aging

Ling, Z., Liu, X., Cheng, Y., Yan, X., & Wu, S. (2020) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2020.1867054 · Cited by 366 · see citing works

The impact of the microbiota-gut-brain axis on Alzheimer’s disease pathophysiology

Doifode, T., Giridharan, V. V., Generoso, J. S., Bhatti, G., Collodel, A., Schulz, P. E., Forlenza, O. V., & Barichello, T. (2021) · Pharmacological Research · doi:10.1016/j.phrs.2020.105314 · Cited by 347 · see citing works

Interplay of gut microbiota and oxidative stress: Perspective on neurodegeneration and neuroprotection

Shandilya, S., Kumar, S., Jha, N. K., Kesari, K. K., & Ruokolainen, J. (2021) · Journal of Advanced Research · doi:10.1016/j.jare.2021.09.005 · Cited by 300 · see citing works

Gut microbes and muscle function: can probiotics make our muscles stronger?

Giron, M., Thomas, M., Dardevet, D. P., Chassard, C., & Savary‐Auzeloux, I. (2022) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.12964 · Cited by 195 · see citing works

Obesity as a risk factor for COVID-19: an overview

Alberca, R. W., Oliveira, L. D. M., Branco, A. C. C. C., Pereira, N. Z., & Sato, M. N. (2020) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2020.1775546 · Cited by 187 · see citing works

The Skin Microbiome: Current Landscape and Future Opportunities

Smythe, P., & Wilkinson, H. N. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24043950 · Cited by 208 · see citing works

Alterations in intestinal microbiota diversity, composition, and function in patients with sarcopenia

Kang, L., Li, P., Wang, D., Wang, T., Dong, H., & Qu, X. (2021) · Scientific Reports · doi:10.1038/s41598-021-84031-0 · Cited by 190 · see citing works

Skeletal muscle oxidative stress and inflammation in aging: Focus on antioxidant and anti-inflammatory therapy

Chen, M., Wang, Y., Deng, S., Lian, Z., & Yu, K. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.964130 · Cited by 187 · see citing works

Gut microbiota–bile acid–skeletal muscle axis

Mancin, L., Wu, G. D., & Paoli, A. (2022) · Trends in Microbiology · doi:10.1016/j.tim.2022.10.003 · Cited by 176 · see citing works

Chronic Stress-Induced Depression and Anxiety Priming Modulated by Gut-Brain-Axis Immunity

Westfall, S., Caracci, F., Estill, M. S., Frolinger, T., Shen, L., & Pasinetti, G. M. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.670500 · Cited by 142 · see citing works

Role of Bifidobacterium in Modulating the Intestinal Epithelial Tight Junction Barrier: Current Knowledge and Perspectives

Abdulqadir, R. F., Engers, J., & Al–Sadi, R. (2023) · Current Developments in Nutrition · doi:10.1016/j.cdnut.2023.102026 · Cited by 136 · see citing works

The Potential of Lactobacillus spp. for Modulating Oxidative Stress in the Gastrointestinal Tract

Kong, Y., Olejar, K. J., On, S. L. W., & Chelikani, V. (2020) · Antioxidants · doi:10.3390/antiox9070610 · Cited by 125 · see citing works

Tryptophan-rich diet ameliorates chronic unpredictable mild stress induced depression- and anxiety-like behavior in mice: The potential involvement of gut-brain axis

Wang, D., Wu, J., Zhu, P., Xie, H., Lu, L., Bai, W., Pan, W., Shi, R., Ye, J., Xia, B., et al. (2022) · Food Research International · doi:10.1016/j.foodres.2022.111289 · Cited by 112 · see citing works

Population‐based metagenomics analysis reveals altered gut microbiome in sarcopenia: data from the Xiangya Sarcopenia Study

Wang, Y., Zhang, Y., Lane, N. E., Wu, J., Yang, T., Li, J., He, H., Wei, J., Zeng, C., & Lei, G. (2022) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.13037 · Cited by 109 · see citing works

Antidepressant effects of a polysaccharide from okra (Abelmoschus esculentus (L) Moench) by anti-inflammation and rebalancing the gut microbiota

Yan, T., Nian, T., Liao, Z., Xiao, F., Wu, B., Bi, K., He, B., & Jia, Y. (2019) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2019.12.138 · Cited by 109 · see citing works

Impact of probiotics on muscle mass, muscle strength and lean mass: a systematic review and meta‐analysis of randomized controlled trials

Prokopidis, K., Giannos, P., Kirwan, R., Ispoglou, T., Galli, F., Witard, O. C., Triantafyllidis, K. K., Kechagias, K. S., Morwani‐Mangnani, J., Ticinesi, A., et al. (2022) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.13132 · Cited by 111 · see citing works

Genetic and metabolic links between the murine microbiome and memory

Mao, J., Kim, Y., Zhou, Y., Hu, D., Zhong, C., Chang, H., Brislawn, C., Fansler, S. J., Langley, S. A., Wang, Y., et al. (2020) · Microbiome · doi:10.1186/s40168-020-00817-w · Cited by 108 · see citing works

Bisphenol A impairs cognitive function and 5-HT metabolism in adult male mice by modulating the microbiota-gut-brain axis

Ni, Y., Hu, L., Yang, S., Ni, L., Ma, L., Zhao, Y., Zheng, A., Jin, Y., & Fu, Z. (2021) · Chemosphere · doi:10.1016/j.chemosphere.2021.130952 · Cited by 105 · see citing works

The Role of the Gut Microbiome on Skeletal Muscle Mass and Physical Function: 2019 Update

Lustgarten, M. S. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2019.01435 · Cited by 105 · see citing works

Depletion of gut microbiota induces skeletal muscle atrophy by FXR-FGF15/19 signalling

Qiu, Y., Yu, J., Li, Y., Yang, F., Yu, H., Xue, M., Zhang, F., Jiang, X., Ji, X., & Bao, Z. (2021) · Annals of Medicine · doi:10.1080/07853890.2021.1900593 · Cited by 105 · see citing works

Gut Microbiota Interaction with the Central Nervous System throughout Life

Ojeda, J., Ávila, A., & Vidal, P. M. (2021) · Journal of Clinical Medicine · doi:10.3390/jcm10061299 · Cited by 107 · see citing works

Ganoderic acid A from Ganoderma lucidum protects against alcoholic liver injury through ameliorating the lipid metabolism and modulating the intestinal microbial composition

Lv, X., Wu, Q., Cao, Y.-J., Lin, Y., Guo, W., Rao, P., Zhang, Y., Chen, Y., Ai, L., & Ni, L. (2022) · Food & Function · doi:10.1039/d1fo03219d · Cited by 104 · see citing works

Mechanisms Linking the Gut-Muscle Axis With Muscle Protein Metabolism and Anabolic Resistance: Implications for Older Adults at Risk of Sarcopenia

Prokopidis, K., Chambers, E. S., Lochlainn, M. N., & Witard, O. C. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.770455 · Cited by 109 · see citing works

PPARs and Microbiota in Skeletal Muscle Health and Wasting

Manickam, R., Duszka, K., & Wahli, W. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21218056 · Cited by 98 · see citing works

Bifidobacterium and Lactobacillus improve inflammatory bowel disease in zebrafish of different ages by regulating the intestinal mucosal barrier and microbiota

Ni, Y., Zhang, Y., Zheng, L., Rong, N., Yang, Y., Gong, P., Yang, Y. M., Siwu, X., Zhang, C., Zhu, L., et al. (2023) · Life Sciences · doi:10.1016/j.lfs.2023.121699 · Cited by 89 · see citing works

Advances in Fecal Microbiota Transplantation for Gut Dysbiosis‐Related Diseases

Hou, S., Yu, J., Li, Y., Zhao, D., & Zhang, Z. (2025) · Advanced Science · doi:10.1002/advs.202413197 · Cited by 93 · see citing works

Alleviation of cognitive impairment by gut microbiota lipopolysaccharide production-suppressing Lactobacillus plantarum and Bifidobacterium longum in mice

Lee, D.-Y., Shin, Y.-J., Kim, J.-K., Jang, H., Joo, M.-K., & Kim, D. (2021) · Food & Function · doi:10.1039/d1fo02167b · Cited by 71 · see citing works

Exploring the Relationship between the Gut Microbiota and Ageing: A Possible Age Modulator

Salazar, J., Durán, P., Díaz, M. P., Chacín, M., Santeliz, R., Mengual, E., Gutiérrez, E., León, X., Díaz, A., Bernal, M., et al. (2023) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph20105845 · Cited by 71 · see citing works

Probiotic Bifidobacterium breve MCC1274 Mitigates Alzheimer’s Disease-Related Pathologies in Wild-Type Mice

Abdelhamid, M., Zhou, C., Jung, C., & Michikawa, M. (2022) · Nutrients · doi:10.3390/nu14122543 · Cited by 68 · see citing works

Mechanisms Involved in Gut Microbiota Regulation of Skeletal Muscle

Li, G., Jin, B., & Fan, Z. (2022) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2022/2151191 · Cited by 71 · see citing works

The gut metabolite 3-hydroxyphenylacetic acid rejuvenates spermatogenic dysfunction in aged mice through GPX4-mediated ferroptosis

Jin, Z., Yang, Y., Cao, Y., Wen, Q., Xi, Y., Cheng, J., Zhao, Q., Weng, J., Hong, K., Jiang, H., et al. (2023) · Microbiome · doi:10.1186/s40168-023-01659-y · Cited by 68 · see citing works

Achieving healthy aging through gut microbiota-directed dietary intervention: Focusing on microbial biomarkers and host mechanisms

Xiao, Y., Feng, Y., Zhao, J., Chen, W., & Lu, W. (2024) · Journal of Advanced Research · doi:10.1016/j.jare.2024.03.005 · Cited by 75 · see citing works

Interactions between gut microbiota and skeletal muscle

Gizard, F., Fernandez, A., & Vadder, F. D. (2020) · Nutrition and Metabolic Insights · doi:10.1177/1178638820980490 · Cited by 66 · see citing works

Interplay of good bacteria and central nervous system: cognitive aspects and mechanistic considerations

Salami, M. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.613120 · Cited by 67 · see citing works

An Integrated Approach to Skeletal Muscle Health in Aging

Agostini, D., Gervasi, M., Ferrini, F., Bartolacci, A., Stranieri, A., Piccoli, G., Barbieri, E., Sestili, P., Patti, A., Stocchi, V., et al. (2023) · Nutrients · doi:10.3390/nu15081802 · Cited by 76 · see citing works

Age-Related Dysfunction in Proteostasis and Cellular Quality Control in the Development of Sarcopenia

Paez, H., Pitzer, C. R., & Alway, S. (2023) · Cells · doi:10.3390/cells12020249 · Cited by 66 · see citing works

Role of Probiotics, Prebiotics, and Synbiotics in the Elderly: Insights Into Their Applications

Ale, E. C., & Binetti, A. G. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.631254 · Cited by 64 · see citing works

Gut Microbiota Markers and Dietary Habits Associated with Extreme Longevity in Healthy Sardinian Centenarians

Palmas, V., Pisanu, S., Madau, V., Casula, E., Deledda, A., Cusano, R., Uva, P., Loviselli, A., Velluzzi, F., & Manzin, A. (2022) · Nutrients · doi:10.3390/nu14122436 · Cited by 67 · see citing works

Progress of linking gut microbiota and musculoskeletal health: casualty, mechanisms, and translational values

Wang, Y., Li, Y., Bo, L., Zhou, E., Chen, Y., Naranmandakh, S., Xie, W., Ru, Q., Chen, L., Zhu, Z., et al. (2023) · Gut Microbes · doi:10.1080/19490976.2023.2263207 · Cited by 64 · see citing works

Nutraceuticals in the Prevention and Treatment of the Muscle Atrophy

Wang, Y., Liu, Q., Quan, H., Kang, S.-G., Huang, K., & Tong, T. (2021) · Nutrients · doi:10.3390/nu13061914 · Cited by 61 · see citing works

Gut microbiota and anti-aging: Focusing on spermidine

Yu, L., Pan, J., Guo, M., Duan, H., Zhang, H., Narbad, A., Zhai, Q., Tian, F., & Chen, W. (2023) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2023.2224867 · Cited by 62 · see citing works

Spermidine ameliorates high-fat diet-induced hepatic steatosis and adipose tissue inflammation in preexisting obese mice

Ma, L., Ni, Y., Hu, L., Zhao, Y., Zheng, L., Yang, S. T., Ni, L., & Fu, Z. (2020) · Life Sciences · doi:10.1016/j.lfs.2020.118739 · Cited by 59 · see citing works

The Role of Bifidobacteria in Predictive and Preventive Medicine: A Focus on Eczema and Hypercholesterolemia

Marras, L., Caputo, M., Bisicchia, S., Soato, M., Bertolino, G., Vaccaro, S., & Inturri, R. (2021) · Microorganisms · doi:10.3390/microorganisms9040836 · Cited by 60 · see citing works

Association between gut microbiota and psychiatric disorders: a systematic review

Valle, C. G.-D., Fernández, J., Solá, E., Montoya‐Castilla, I., Morillas, C., & Bañuls, C. (2023) · Frontiers in Psychology · doi:10.3389/fpsyg.2023.1215674 · Cited by 61 · see citing works

Lactobacillus plantarum GKM3 Promotes Longevity, Memory Retention, and Reduces Brain Oxidation Stress in SAMP8 Mice

Lin, S.-W., Tsai, Y., Chen, Y., Wang, M.-F., Chen, C., Lin, W., & Fang, T. J. (2021) · Nutrients · doi:10.3390/nu13082860 · Cited by 56 · see citing works

Bifidobacterium animalis subsp. lactis lkm512 Attenuates Obesity‐Associated Inflammation and Insulin Resistance Through the Modification of Gut Microbiota in High‐Fat Diet‐Induced Obese Mice

Ma, L., Zheng, A., Ni, L., Wu, L., Hu, L., Zhao, Y., Fu, Z., & Ni, Y. (2021) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.202100639 · Cited by 56 · see citing works

Gut microbes-muscle axis in muscle function and meat quality

He, Y., Hu, H., Liang, X., Liang, J., Li, F., & Zhou, X. (2025) · Science China Life Sciences · doi:10.1007/s11427-024-2885-4 · Cited by 57 · see citing works

The Gut Microbiota and Its Metabolites, Novel Targets for Treating and Preventing Non‐Alcoholic Fatty Liver Disease

Ni, Y., Ni, L., Zhuge, F., & Fu, Z. (2020) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.202000375 · Cited by 53 · see citing works

The Effects of Pro-, Pre-, and Synbiotics on Muscle Wasting, a Systematic Review—Gut Permeability as Potential Treatment Target

van Krimpen, S. J., Jansen, F. A. C., Ottenheim, V. L., Belzer, C., van der Ende, M., & van Norren, K. (2021) · Nutrients · doi:10.3390/nu13041115 · Cited by 53 · see citing works

Effects of probiotics supplementation on dementia and cognitive impairment: A systematic review and meta-analysis of preclinical and clinical studies

Ruiz‐González, C., Román, P., Rueda‐Ruzafa, L., Rodríguez-Arrastia, M. J., & Cardona, D. (2020) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2020.110189 · Cited by 53 · see citing works

The Effect of Probiotics on Health Outcomes in the Elderly: A Systematic Review of Randomized, Placebo-Controlled Studies

Hutchinson, A. N., Bergh, C., Krüger, K., Sűsserová, M., Allen, J., Améen, S., & Tingö, L. (2021) · Microorganisms · doi:10.3390/microorganisms9061344 · Cited by 54 · see citing works

Common Inflammatory Mechanisms in COVID-19 and Parkinson’s Diseases: The Role of Microbiome, Pharmabiotics and Postbiotics in Their Prevention

Danilenko, V., Devyatkin, A., Marsova, M., Shibilova, M., Ilyasov, R. A., & Shmyrev, V. (2021) · Journal of Inflammation Research · doi:10.2147/jir.s333887 · Cited by 53 · see citing works

Fucoxanthin has potential for therapeutic efficacy in neurodegenerative disorders by acting on multiple targets

Yang, M., Xuan, Z., Wang, Q., Yan, S., Zhou, D., Naman, C. B., Zhang, J., He, S., Yan, X., & Cui, W. (2021) · Nutritional Neuroscience · doi:10.1080/1028415x.2021.1926140 · Cited by 43 · see citing works

5‐Heptadecylresorcinol, a Biomarker for Whole Grain Rye Consumption, Ameliorates Cognitive Impairments and Neuroinflammation in APP/PS1 Transgenic Mice

Liu, J., Wang, Y., Wang, Z., Hao, Y., Bai, W.-Z., Wang, Z., & Wang, J. (2020) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201901218 · Cited by 43 · see citing works

Plant Polyphenols Attenuate DSS-induced Ulcerative Colitis in Mice via Antioxidation, Anti-inflammation and Microbiota Regulation

Chen, H., Li, Y., Wang, J., Zheng, T., Wu, C., Cui, M., Feng, Y., Ye, H., Dong, Z., & Dang, Y. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241310828 · Cited by 41 · see citing works

Biological Functions and Cross-Kingdom Host Gene Regulation of Small RNAs in Lactobacillus plantarum-Derived Extracellular Vesicles

Yu, S., Zhao, Z., Hao, P., Yan, Q., Zhao, M., Zhou, G., Zhang, C., Kang, J., & Li, P. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.944361 · Cited by 40 · see citing works

Benign regulation of the gut microbiota: The possible mechanism through which the beneficial effects of manual acupuncture on cognitive ability and intestinal mucosal barrier function occur in APP/PS1 mice

Hao, X., Ding, N., Zhang, Y., Yang, Y., Zhao, Y., Zhao, J. J., Li, Y., & Li, Z. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.960026 · Cited by 40 · see citing works

Organophosphate Insecticide Malathion Induces Alzheimer’s Disease-Like Cognitive Impairment in Mice: Evidence of the Microbiota-Gut-Brain Axis

Cui, J., Xiao, S., Cao, Y., Zhang, Y., Yang, J., Zheng, L., Zhao, F., Liu, X., Liu, D., Zhou, Z., et al. (2024) · Environmental Science & Technology · doi:10.1021/acs.est.4c07427 · Cited by 41 · see citing works

Bifidobacterium as a Potential Biomarker of Sarcopenia in Elderly Women

Wang, Z., Xu, X., Deji, Y., Gao, S., Wu, C., Song, Q., Shi, Z., Xiang, X., Zang, J., & Su, J. (2023) · Nutrients · doi:10.3390/nu15051266 · Cited by 38 · see citing works

Pharmacological activation of REV-ERBα improves nonalcoholic steatohepatitis by regulating intestinal permeability

Ni, Y., Zhao, Y., Ma, L., Wang, Z., Ni, L., Hu, L., & Fu, Z. (2020) · Metabolism · doi:10.1016/j.metabol.2020.154409 · Cited by 38 · see citing works

Impact of Gut Microbiota on the Peripheral Nervous System in Physiological, Regenerative and Pathological Conditions

Calabrò, S., Kankowski, S., Cescon, M., Gambarotta, G., Raimondo, S., Haastert‐Talini, K., & Ronchi, G. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24098061 · Cited by 38 · see citing works

Nutritional Strategies for Muscle Atrophy: Current Evidence and Underlying Mechanisms

Shen, Y., Zhang, C., Dai, C., Zhang, Y., Wang, K., Gao, Z., Chen, X., Yang, X., Sun, H., Yao, X., et al. (2024) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.202300347 · Cited by 37 · see citing works

Effect of dendrobium mixture in alleviating diabetic cognitive impairment associated with regulating gut microbiota

Zheng, Y., Zhou, X., Wang, C., Zhang, J., Chang, D., Zhuang, S., Xu, W., Chen, Y., Wang, X., Nan, L., et al. (2022) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2022.112891 · Cited by 37 · see citing works

Can probiotics, prebiotics and synbiotics improve functional outcomes for older people: a systematic review

Coutts, L., Ibrahim, K., Tan, Q. Y., Lim, S. E. R., Cox, N. J., & Roberts, H. C. (2020) · European Geriatric Medicine · doi:10.1007/s41999-020-00396-x · Cited by 33 · see citing works

Exposure to polystyrene microplastics reduces sociality and brain oxytocin levels through the gut-brain axis in mice

Wang, L., Li, S., Hao, Y., Liu, X., Liu, Y., Zuo, L., Tai, F., Yin, L., Young, L. J., & Li, D. (2024) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2024.174026 · Cited by 37 · see citing works

Bifidobacterium adolescentis-derived nicotinic acid improves host skeletal muscle mitochondrial function to ameliorate sarcopenia

Zhang, Z., Guo, Q., Yang, Z., Sun, Y., Jiang, S., He, Y., Li, J., & Zhang, J. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.115265 · Cited by 35 · see citing works

A narrative review on the use of probiotics in several diseases. Evidence and perspectives

Campaniello, D., Bevilacqua, A., Speranza, B., Racioppo, A., Sinigaglia, M., & Corbo, M. R. (2023) · Frontiers in Nutrition · doi:10.3389/fnut.2023.1209238 · Cited by 36 · see citing works

Unraveling the Microbiome–Human Body Axis: A Comprehensive Examination of Therapeutic Strategies, Interactions and Implications

Olteanu, G., Pană, M.-A., Busnatu, Ș., Lupuliasa, D., Neacșu, S. M., Mititelu, M., Musuc, A. M., Ioniță-Mîndrican, C.-B., & Boroghină, S. C. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25105561 · Cited by 34 · see citing works

Microbiota Targeted Interventions of Probiotic Lactobacillus as an Anti-Ageing Approach: A Review

Ishaq, M., Khan, A., Bacha, A. S., Shah, T., Hanif, A., Ahmad, A. A., Ke, W., Li, F., Din, A. U., Ding, Z., et al. (2021) · Antioxidants · doi:10.3390/antiox10121930 · Cited by 34 · see citing works

Centenarian-Sourced Lactobacillus casei Combined with Dietary Fiber Complex Ameliorates Brain and Gut Function in Aged Mice

Ren, M., Li, H., Fu, Z., & Li, Q. (2022) · Nutrients · doi:10.3390/nu14020324 · Cited by 34 · see citing works

Fecal microbiota transplantation, a tool to transfer healthy longevity

Novelle, M. G., Naranjo-Martínez, B., Lopez-Canovas, J. L., & Díaz‐Ruiz, A. (2024) · Ageing Research Reviews · doi:10.1016/j.arr.2024.102585 · Cited by 34 · see citing works

Presence of Blastocystis in gut microbiota is associated with cognitive traits and decreased executive function

Mayneris‐Perxachs, J., Arnoriaga‐Rodríguez, M., Garre‐Olmo, J., Puig, J., Ramos, R., Trelis, M., Burokas, A., Coll, C., Zapata-Tona, C., Pedraza, S., et al. (2022) · The ISME Journal · doi:10.1038/s41396-022-01262-3 · Cited by 35 · see citing works

Increase in muscle mass associated with the prebiotic effects of 1-kestose in super-elderly patients with sarcopenia

Tominaga, K., Tsuchiya, A., Nakano, O., Kuroki, Y., Oka, K., Minemura, A., Matsumoto, A., Takahashi, M., Kadota, Y., Tochio, T., et al. (2021) · Bioscience of Microbiota Food and Health · doi:10.12938/bmfh.2020-063 · Cited by 32 · see citing works

Red Cabbage Anthocyanins Attenuate Cognitive Impairment By Attenuating Neuroinflammation and Regulating Gut Microbiota in Aging Mice

Zhang, N., & Jing, P. (2023) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.3c03183 · Cited by 31 · see citing works

Nutritional Value of Yogurt as a Protein Source: Digestibility/Absorbability and Effects on Skeletal Muscle

Sumi, K., Tagawa, R., Yamazaki, K., Nakayama, K., Ichimura, T., Sanbongi, C., & Nakazato, K. (2023) · Nutrients · doi:10.3390/nu15204366 · Cited by 31 · see citing works

Protective effects of camellia and olive oils against cognitive impairment via gut microbiota-brain communication in rats

Chen, S.-Y., Weng, M.-H., Li, Z., Wang, G., & Yen, G. (2022) · Food & Function · doi:10.1039/d1fo04418d · Cited by 31 · see citing works

Agaricus bisporus Polysaccharides Ameliorates Behavioural Deficits in D-Galactose-Induced Aging Mice: Mediated by Gut Microbiota

Duan, H., Li, J., & Fan, L. (2023) · Foods · doi:10.3390/foods12020424 · Cited by 31 · see citing works

Probiotics Supplements Improve the Sarcopenia-Related Quality of Life in Older Adults with Age-Related Muscle Decline

Qaisar, R., Burki, A., Karim, A., Iqbal, M. S., & Ahmad, F. (2024) · Calcified Tissue International · doi:10.1007/s00223-024-01211-6 · Cited by 30 · see citing works

The gut core microbial species Bifidobacterium longum: Colonization, mechanisms, and health benefits

Xiao, Y., Huang, L., Zhao, J., Chen, W., & Lu, W. (2024) · Microbiological Research · doi:10.1016/j.micres.2024.127966 · Cited by 31 · see citing works

Long-term silk peptide intake promotes skeletal muscle mass, reduces inflammation, and modulates gut microbiota in middle-aged female rats

Park, S., Yuan, H., Zhang, T., Wu, X., Huang, S. K., & Cho, S. M. (2021) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2021.111415 · Cited by 30 · see citing works

Metagenomic and Transcriptomic Analyses Reveal the Differences and Associations Between the Gut Microbiome and Muscular Genes in Angus and Chinese Simmental Cattle

Ya, Z., Chen, J., Wang, X., Han, L., Yang, Y., Wang, Q., & Yu, Q. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.815915 · Cited by 31 · see citing works

How Diet and Lifestyle Can Fine-Tune Gut Microbiomes for Healthy Aging

Tamayo, M., Olivares, M., Ruas‐Madiedo, P., Margollés, A., Espı́n, J. C., Medina, I., Moreno-Arribas, M. V., Canals, S., Mirasso, C. R., Ortín, S., et al. (2024) · Annual Review of Food Science and Technology · doi:10.1146/annurev-food-072023-034458 · Cited by 33 · see citing works

The gut microbiome, chronic kidney disease, and sarcopenia

Zheng, G., Cao, J., Wang, X. H., He, W., & Wang, B. (2024) · Cell Communication and Signaling · doi:10.1186/s12964-024-01922-1 · Cited by 29 · see citing works

Probiotic supplementation demonstrates therapeutic potential in treating gut dysbiosis and improving neurocognitive function in age-related dementia

Meng, H. Y. H., Mak, C. C. H., Mak, J. W. Y., Zuo, T., Ko, H., & Chan, F. K. L. (2022) · European Journal of Nutrition · doi:10.1007/s00394-021-02760-4 · Cited by 28 · see citing works

Amelioration of Ovalbumin-Induced Food Allergy in Mice by Targeted Rectal and Colonic Delivery of Cyanidin-3-O-Glucoside

Li, J., Zou, C., & Liu, Y. (2022) · Foods · doi:10.3390/foods11111542 · Cited by 28 · see citing works

Gut microbiota–astrocyte axis: new insights into age-related cognitive decline

Zhang, L., Wei, J., Liu, X., Li, D., Pang, X., Chen, F., Cao, H., & Lei, P. (2024) · Neural Regeneration Research · doi:10.4103/nrr.nrr-d-23-01776 · Cited by 28 · see citing works

Dysbiosis, Host Metabolism, and Non-communicable Diseases: Trialogue in the Inborn Errors of Metabolism

Montanari, C., Parolisi, S., Borghi, E., Putignani, L., Bassanini, G., Zuvadelli, J., Bonfanti, C., Tummolo, A., Dionisi‐Vici, C., Biasucci, G., et al. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.716520 · Cited by 27 · see citing works

Heat-Killed Lactiplantibacillus plantarum LRCC5314 Mitigates the Effects of Stress-Related Type 2 Diabetes in Mice via Gut Microbiome Modulation

Nam, Y., Yoon, S., Baek, J., Kim, J., Park, M., Hwang, K., & Kim, W. (2022) · Journal of Microbiology and Biotechnology · doi:10.4014/jmb.2111.11008 · Cited by 27 · see citing works

Effect of Lotus Seed Resistant Starch on Lactic Acid Conversion to Butyric Acid Fermented by Rat Fecal Microbiota

Wang, Z., Lin, Y., Liu, L., Zheng, B., Zhang, Y., & Zeng, H. (2022) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.1c06000 · Cited by 26 · see citing works

Bifidobacterium bifidum BGN4 and Bifidobacterium longum BORI promotes neuronal rejuvenation in aged mice

Kim, H., Shin, J., Kim, S., Kim, S., Cho, B., Park, S., Park, G., Shin, H., Park, M. S., & Kim, J. (2022) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2022.03.024 · Cited by 26 · see citing works

Association between Gut Microbiota and Body Composition in Japanese General Population: A Focus on Gut Microbiota and Skeletal Muscle

Sugimura, Y., Kanda, A., Sawada, K., Wai, K. M., Tanabu, A., Ozato, N., Midorikawa, T., Hisada, T., Nakaji, S., & Ihara, K. (2022) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph19127464 · Cited by 27 · see citing works

Mechanism Explanation on Improved Cognitive Ability of D -Gal Inducing Aged Mice Model by Lactiplantibacillus plantarum MWFLp-182 via the Microbiota–Gut–Brain Axis

Nie, H., Wang, X., Luo, Y., Kong, F., Mu, G., & Wu, X. (2024) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.3c09675 · Cited by 26 · see citing works

Navigating the Intersection: Sarcopenia and Sarcopenic Obesity in Inflammatory Bowel Disease

Calvez, V., Becherucci, G., Covello, C., Piccirilli, G., Mignini, I., Esposto, G., Laterza, L., Ainora, M. E., Scaldaferri, F., Gasbarrini, A., et al. (2024) · Biomedicines · doi:10.3390/biomedicines12061218 · Cited by 25 · see citing works

Probiotics and muscle health: the impact of Lactobacillus on sarcopenia through the gut-muscle axis

Zhu, J., Peng, F., Yang, H., Luo, J., Zhang, L., Chen, X., Liao, H., Lei, H., Liu, S., Yang, T., et al. (2025) · Frontiers in Microbiology · doi:10.3389/fmicb.2025.1559119 · Cited by 26 · see citing works

The microbiota-gut- hippocampus axis

Salami, M., & Soheili, M. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.1065995 · Cited by 27 · see citing works

Ameliorative Effect of Ellagic Acid on Aging in Rats with the Potential Mechanism Relying on the Gut Microbiota and Urolithin A-Producing Ability

Xian, W., Deng, Y., Yang, Y., Tan, Z., Chen, C., Li, W., & Yang, R. (2023) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.3c00960 · Cited by 28 · see citing works

Centenarian-Sourced Lactobacillus casei Combined with Dietary Fiber Complex Ameliorates Brain and Gut Function in Aged Mice

Ren, M., Li, H., Fu, Z., & Li, Q. (2022) · Nutrients · doi:10.3390/nu14020324 · Cited by 34 · see citing works

Bifidobacterium bifidum and Lactobacillus paracasei alleviate sarcopenia and cognitive impairment in aged mice by regulating gut microbiota-mediated AKT, NF-κB, and FOXO3a signaling pathways

Baek, J.-S., Shin, Y.-J., Ma, X., Park, H.-S., Hwang, Y.-H., & Kim, D. (2023) · Immunity & Ageing · doi:10.1186/s12979-023-00381-5 · Cited by 53 · see citing works

Probiotics Ameliorate Aging-Related Cognitive Impairments and Pathological Changes through Alleviating Telomere Attrition and Enhancing Mitochondrial Function in Senescence-Accelerated Mouse Prone 8 Mice

Zhou, S., Shan, S., Li, R., Wang, X., Xiong, J., & Cheng, G. (2025) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.5c09572 · Cited by 6 · see citing works

Antiaging Effects of Human Fecal Transplants with Different Combinations of Bifidobacterium bifidum LTBB21J1 and Lactobacillus casei LTL1361 in d -Galactose-Induced Mice

Zhou, F., Zhang, Q., Zheng, X., Shi, F., Ma, K., Ji, F., Meng, N., Li, R., Lv, J., & Li, Q. (2024) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.3c09815 · Cited by 13 · see citing works

Lactobacillus plantarum LLY-606 Supplementation Ameliorates the Cognitive Impairment of Natural Aging in Mice: The Potential Role of Gut Microbiota Homeostasis

Shi, R., Jin, Y., Fan, H., Hu, X., Wu, X., Wang, D., Zhao, B., Dai, X., & Liu, X. (2024) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.3c07041 · Cited by 19 · see citing works