The DOI matches its Crossref record; 18 of the 18 references it cites were found in a registry or an index.
Effects of intraduodenal injection of Lactobacillus johnsonii La1 on renal sympathetic nerve activity and blood pressure in urethane-anesthetized rats.
Abstract
Previously, it was shown that milk fermented with lactic acid bacteria lowers blood pressure, suggesting that metabolites or components of the bacteria have hypotensive action. To examine whether one of lactobacilli, Lactobacillus johnsonii La1 (LJLa1), a probiotic strain adhesive onto intestinal epithelial cells, or its metabolite has hypotensive action, and if so the mechanism of action, we determined the effects of intraduodenal injection of LJLa1 on blood pressure (BP) and the activity of autonomic nerves in urethane-anesthetized rats. Intraduodenal injection of LJLa1 reduced renal sympathetic nerve activity (RSNA) and BP and enhanced gastric vagal nerve activity (GVNA). Pre-treatment with thioperamide, a histaminergic H3-receptor antagonist, eliminated the effects of LJLa1 on RSNA, GVNA, and BP. Furthermore, bilateral lesions of the hypothalamic suprachiasmatic nucleus (SCN), the master circadian oscillator, abolished the suppression of RSNA and BP and the elevation of GVNA caused by LJLa1. These findings suggest that LJLa1 or its metabolites might lower BP by changing autonomic neurotransmission via the central histaminergic nerves and the suprachiasmatic nucleus in rats.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“It has become apparent that commensal bacteria can signal to local sensory neurons to alter their excitability state, which itself can last long after the bacteria have been removed (Tanida et al., 2005)”
From The Microbiota-Gut-Brain Axis (2019) · cites this paper as Tanida et al., 2005
Citations
Cites
The rat brain in stereotaxic coordinates
Palkovits, M. (1983) · Neuropeptides · doi:10.1016/0143-4179(83)90049-5 · Cited by 28,959
The Rat Brain in Stereotaxic Coordinates
Paxinos, G., & Watson, C. (1983) · Elsevier eBooks · doi:10.1016/c2009-0-63235-9 · Cited by 28,585
Auto-inhibition of brain histamine release mediated by a novel class (H3) of histamine receptor
Arrang, J., Garbarg, M., & Schwartz, J. (1983) · Nature · doi:10.1038/302832a0 · Cited by 1,584
Seppo, L., Jauhiainen, T., Poussa, T. A., & Korpela, R. (2003) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/77.2.326 · Cited by 670
A detailed mapping of the histamine H3 receptor and its gene transcripts in rat brain
Pillot, C., Héron, A., Cochois, V., Tardivel‐Lacombe, J., Ligneau, X., Schwartz, J. C., & Arrang, J. M. (2002) · Neuroscience · doi:10.1016/s0306-4522(02)00135-5 · Cited by 340
Probiotics, infection and immunity
Macfarlane, G. T., & Cummings, J. H. (2002) · Current Opinion in Infectious Diseases · doi:10.1097/00001432-200210000-00008 · Cited by 185
Sipola, M., Finckenberg, P., Santisteban, J., Korpela, R., Vapaatalo, H., & Nurminen, M. L. (2001) · PubMed · Cited by 162
Chapter 8 Role of medulla oblongata in generation of sympathetic and vagal outflows
Guyenet, P. G., Koshiya, N., Huangfu, D., Baraban, S. C., Stornetta, R. L., & Li, Y. (1996) · Progress in brain research · doi:10.1016/s0079-6123(08)61862-2 · Cited by 147
Nagai, K., Nagai, N., Shimizu, K., Chun, S.-J., Nakagawa, H., & Niijima, A. (1996) · Progress in brain research · doi:10.1016/s0079-6123(08)60413-6 · Cited by 143
Self-citationSubstance P in the nucleus of the solitary tract augments bronchopulmonary C fiber reflex output
Mutoh, T., Bonham, A. C., & Joad, J. P. (2000) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.2000.279.4.r1215 · Cited by 102
Research works printed but not linked: 1
- T. Yamano, H. Iino, M. Takada, S. Blum, F. Rochat, Y. Fukushima, Improvement of the human intestinal microflora by ingestion of the probiotic strain Lactobacillus johnsonii, Br. J. Nutr., in press.
Cited by
Sorted by citations
Cryan, J. F., O'Riordan, K. J., Cowan, C. S. M., Sandhu, K. V., Bastiaanssen, T. F. S., Boehme, M., Codagnone, M. G., Cussotto, S., Fulling, C., Golubeva, A. V., et al. (2019) · Physiological Reviews · doi:10.1152/physrev.00018.2018 · Cited by 5,286
Mind-altering microorganisms: the impact of the gut microbiota on brain and behaviour
Cryan, J. F., & Dinan, T. G. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3346 · Cited by 4,572
Gut microbiota in cardiovascular health and disease
Tang, W. H. W., Kitai, T., & Hazen, S. L. (2017) · Circulation Research · doi:10.1161/circresaha.117.309715 · Cited by 1,670
Gut/brain axis and the microbiota
Mayer, E. A., Tillisch, K., & Gupta, A. (2015) · Journal of Clinical Investigation · doi:10.1172/jci76304 · Cited by 1,503
The vagus nerve at the interface of the microbiota-gut-brain axis
Bonaz, B., Bazin, T., & Pellissier, S. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00049 · Cited by 1,397
Martin, C. R., Osadchiy, V., Kalani, A., & Mayer, E. A. (2018) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2018.04.003 · Cited by 1,284
Bercik, P., Park, A. J., Sinclair, D., Khoshdel, A., Lu, J., Huang, X., Deng, Y., Blennerhassett, P. A., Fahnestock, M., Moine, D., et al. (2011) · Neurogastroenterology & Motility · doi:10.1111/j.1365-2982.2011.01796.x · Cited by 1,018
Collins, S. M., & Bercik, P. (2009) · Gastroenterology · doi:10.1053/j.gastro.2009.01.075 · Cited by 612
Vagal pathways for microbiome-brain-gut axis communication
Forsythe, P., Bienenstock, J., & Kunze, W. A. (2014) · Advances in Experimental Medicine and Biology · doi:10.1007/978-1-4939-0897-4_5 · Cited by 576
Microbiome–microglia connections via the gut–brain axis
Abdel-Haq, R., Schlachetzki, J. C. M., Glass, C. K., & Mazmanian, S. K. (2019) · Journal of Experimental Medicine · doi:10.1084/jem.20180794 · Cited by 471
“Oral inoculation with the pathogen Campylobacter jejuni or intraduodenal injection of the probiotic strain Lactobacillus johnsonii are sufficient to induce activation of vagal sensory neurons innervating the GI tract, as well as neurons in the brainstem (Goehler et al., 2005; Tanida et al., 2005).”
BackgroundDysbiosis of gut microbiota and microbial metabolites in Parkinson's disease
Sun, M.-F., & Shen, Y.-Q. (2018) · Ageing Research Reviews · doi:10.1016/j.arr.2018.04.004 · Cited by 445
Forsythe, P., Sudo, N., Dinan, T., Taylor, V. H., & Bienenstock, J. (2010) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2009.05.058 · Cited by 429
Savignac, H. M., Kiely, B., Dinan, T. G., & Cryan, J. F. (2014) · Neurogastroenterology & Motility · doi:10.1111/nmo.12427 · Cited by 418
Gut Microbiota in Hypertension and Atherosclerosis: A Review
Verhaar, B. J. H., Prodan, A., Nieuwdorp, M., & Muller, M. (2020) · Nutrients · doi:10.3390/nu12102982 · Cited by 425
Beyond gut feelings: how the gut microbiota regulates blood pressure
Marques, F. Z., Mackay, C. R., & Kaye, D. M. (2017) · Nature Reviews Cardiology · doi:10.1038/nrcardio.2017.120 · Cited by 408
Voices from within: gut microbes and the CNS
Forsythe, P., & Kunze, W. A. (2013) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-012-1028-z · Cited by 336
The Microbiota–Gut–Brain Axis and Alzheimer’s Disease: Neuroinflammation Is to Blame?
Megur, A., Baltriukienė, D., Bukelskienė, V., & Burokas, A. (2020) · Nutrients · doi:10.3390/nu13010037 · Cited by 323
Role of Microbiota-Gut-Brain Axis in Regulating Dopaminergic Signaling
Hamamah, S., Aghazarian, A., Nazaryan, A., Hajnal, A. S., & Covașă, M. (2022) · Biomedicines · doi:10.3390/biomedicines10020436 · Cited by 327
The Gut Microbiota (Microbiome) in Cardiovascular Disease and Its Therapeutic Regulation
Rahman, M. M., Islam, F., Harun-Or-Rashid, M., Mamun, A. A., Rahaman, M. S., Islam, M. M., Meem, A. F. K., Sutradhar, P. R., Mitra, S., Mimi, A. A., et al. (2022) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2022.903570 · Cited by 272
Communication of gut microbiota and brain via immune and neuroendocrine signaling
Kasarełło, K., Cudnoch‐Jędrzejewska, A., & Czarzasta, K. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1118529 · Cited by 283
The role of the gut microbiota in dietary interventions for depression and anxiety
Bear, T. L. K., Dalziel, J. E., Coad, J., Roy, N. C., Butts, C. A., & Gopal, P. K. (2020) · Advances in Nutrition · doi:10.1093/advances/nmaa016 · Cited by 229
Liang, D., Leung, R. K., Guan, W., & Au, W. W. (2018) · Gut Pathogens · doi:10.1186/s13099-018-0230-4 · Cited by 206
Longo, S., Rizza, S., & Federici, M. (2023) · Acta Diabetologica · doi:10.1007/s00592-023-02088-x · Cited by 230
The role of gut microbiota in pathogenesis of Alzheimer's disease
Bostancıklıoğlu, M. (2019) · Journal of Applied Microbiology · doi:10.1111/jam.14264 · Cited by 210
The Gut-Brain Axis, the Human Gut Microbiota and Their Integration in the Development of Obesity
Bliss, E., & Whiteside, E. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.00900 · Cited by 196
The Role of the Gut Microbiome in Diabetes and Obesity-Related Kidney Disease
Zaky, A. A., Glastras, S. J., Wong, M. Y. W., Pollock, C. A., & Saad, S. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22179641 · Cited by 176
Choi, C. H., Jo, S. Y., Park, H. J., Chang, S. K., Byeon, J.-S., & Myung, S.-J. (2011) · Journal of Clinical Gastroenterology · doi:10.1097/mcg.0b013e318204593e · Cited by 144
“Probiotics also inhibit the release of adrenocorticotropic hormone and corticosterone,(40) and provoke behavioral alterations by releasing soluble factors.(41,42) Finally, dosing could have been sufficient to improve patient QOL, but inadequate to improve individual symptoms.”
BackgroundSuda, K., & Matsuda, K. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23031172 · Cited by 154
On communication between gut microbes and the brain
Forsythe, P., Kunze, W. A., & Bienenstock, J. (2012) · Current Opinion in Gastroenterology · doi:10.1097/mog.0b013e3283572ffa · Cited by 137
Antihypertensive Effects of Probiotics
Robles‐Vera, I., Toral, M., Romero, M., Jiménez, R., Sánchez, M., Pérez‐Vizcaíno, F., & Duarte, J. (2017) · Current Hypertension Reports · doi:10.1007/s11906-017-0723-4 · Cited by 138
Impact of Gut Microbiota Composition on Onset and Progression of Chronic Non-Communicable Diseases
Noce, A., Marrone, G., Daniele, F. D., Ottaviani, E., Jones, G. W., Bernini, R., Romani, A., & Rovella, V. (2019) · Nutrients · doi:10.3390/nu11051073 · Cited by 162
Muralitharan, R. R., Jama, H. A., Xie, L., Peh, A., Snelson, M., & Marques, F. Z. (2020) · Hypertension · doi:10.1161/hypertensionaha.120.14473 · Cited by 131
How functional foods play critical roles in human health
Pang, G., Xie, J., Chen, Q., & Zhi-he, H. (2012) · Food Science and Human Wellness · doi:10.1016/j.fshw.2012.10.001 · Cited by 134
The Microbiome-Gut-Brain Axis and Resilience to Developing Anxiety or Depression under Stress
Bear, T., Dalziel, J. E., Coad, J., Roy, N. C., Butts, C. A., & Gopal, P. K. (2021) · Microorganisms · doi:10.3390/microorganisms9040723 · Cited by 136
Santisteban, M. M., Kim, S., Pepine, C. J., & Raizada, M. K. (2016) · Circulation Research · doi:10.1161/circresaha.116.307709 · Cited by 126
Lai, K.-K., Lorca, G. L., & González, C. F. (2009) · Applied and Environmental Microbiology · doi:10.1128/aem.02837-08 · Cited by 121
Fukushima, Y., Miyaguchi, S., Yamano, T., Kaburagi, T., Iino, H., Ushida, K., & Sato, K. (2007) · British Journal Of Nutrition · doi:10.1017/s0007114507764723 · Cited by 116
Self-citationKunugi, H. (2023) · Psychiatry and Clinical Neurosciences · doi:10.1111/pcn.13551 · Cited by 117
Microbiota associated with type 2 diabetes and its related complications
Zhang, Y., & Zhang, H. (2013) · Food Science and Human Wellness · doi:10.1016/j.fshw.2013.09.002 · Cited by 115
The Gut Microbiome as Therapeutic Target in Central Nervous System Diseases: Implications for Stroke
Winek, K., Dirnagl, U., & Meisel, A. (2016) · Neurotherapeutics · doi:10.1007/s13311-016-0475-x · Cited by 108
Tanida, M., Niijima, A., Shen, J., Nakamura, T., & Nagai, K. (2006) · Neuroscience Letters · doi:10.1016/j.neulet.2005.12.076 · Cited by 108
Self-citationWang, B., Mao, Y., Diorio, C. J., Wang, L., Huizinga, J. D., Bienenstock, J., & Kunze, W. (2009) · Neurogastroenterology & Motility · doi:10.1111/j.1365-2982.2009.01384.x · Cited by 106
Onal, E. M., Afşar, B., Covic, A. C., Vaziri, N. D., & Kanbay, M. (2018) · Hypertension Research · doi:10.1038/s41440-018-0144-z · Cited by 108
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 112
Cole‐Jeffrey, C. T., Liu, M., Katovich, M. J., Raizada, M. K., & Shenoy, V. (2015) · Journal of Cardiovascular Pharmacology · doi:10.1097/fjc.0000000000000307 · Cited by 101
Wang, B., Mao, Y., Diorio, C. J., Pasyk, M., Wu, R., Bienenstock, J., & Kunze, W. (2010) · The FASEB Journal · doi:10.1096/fj.09-153841 · Cited by 98
Impact of Probiotics on Risk Factors for Cardiovascular Diseases. A Review
Ebel, B., Lemetais, G., Beney, L., Cachon, R., Sokol, H., Langella, P., & Gervais, P. (2014) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2011.579361 · Cited by 97
Effects of adiponectin on the renal sympathetic nerve activity and blood pressure in rats.
Tanida, M., Shen, J., Horii, Y., Matsuda, M., Kihara, S., Funahashi, T., Shimomura, I., Sawai, H., Fukuda, Y., Matsuzawa, Y., et al. (2007) · PubMed · Cited by 95
Self-citationMa, X., Mao, Y., Wang, B., Huizinga, J. D., Bienenstock, J., & Kunze, W. (2009) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.90511.2008 · Cited by 93
Tanida, M., Shen, J., Maeda, K., Horii, Y., Yamano, T., Fukushima, Y., & Nagai, K. (2008) · Obesity Research & Clinical Practice · doi:10.1016/j.orcp.2008.04.003 · Cited by 93
Self-citationYamano, T., Tanida, M., Niijima, A., Maeda, K., Okumura, N., Fukushima, Y., & Nagai, K. (2006) · Life Sciences · doi:10.1016/j.lfs.2006.06.038 · Cited by 92
Self-citationHord, N. G. (2008) · Annual Review of Nutrition · doi:10.1146/annurev.nutr.28.061807.155402 · Cited by 89
Martin, C. R., & Mayer, E. A. (2017) · Nestlé Nutrition Institute Workshop series · doi:10.1159/000461732 · Cited by 85
Wu, R., Pasyk, M., Wang, B., Forsythe, P., Bienenstock, J., Mao, Y., Sharma, P., Stanisz, A. M., & Kunze, W. (2013) · Neurogastroenterology & Motility · doi:10.1111/nmo.12072 · Cited by 88
Probiotics and blood pressure: current insights
Sudha, R., & Upadrasta, A. (2016) · Integrated Blood Pressure Control · doi:10.2147/ibpc.s73246 · Cited by 88
Defensive responses: behaviour, the brain and the body
Tseng, Y.-T., Schaefke, B., Wei, P., & Wang, L. (2023) · Nature reviews. Neuroscience · doi:10.1038/s41583-023-00736-3 · Cited by 84
Zhang, Y., Guo, X. Q., Guo, J., He, Q., Li, H., Song, Y., & Zhang, H. (2014) · Scientific Reports · doi:10.1038/srep05654 · Cited by 69
Dietary Regulation of Gut-Brain Axis in Alzheimer’s Disease: Importance of Microbiota Metabolites
Frausto, D. M., Forsyth, C. B., Keshavarzian, A., & Voigt, R. M. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.736814 · Cited by 61
Targeting DNA Methylation in the Adult Brain through Diet
Allison, J., Kaliszewska, A., Uceda, S., Reiriz, M., & Arias, N. (2021) · Nutrients · doi:10.3390/nu13113979 · Cited by 65
Pharmacomicrobiomics: Exploiting the Drug-Microbiota Interactions in Antihypertensive Treatment
Chen, H., Gong, J.-Y., Xing, K., Liu, M.-Z., Ren, H., & Luo, J. (2022) · Frontiers in Medicine · doi:10.3389/fmed.2021.742394 · Cited by 59
Dietary Fat Modulation of Gut Microbiota and Impact on Regulatory Pathways Controlling Food Intake
Hamamah, S., Amin, A., Al-Kassir, A. L., Chuang, J., & Covașă, M. (2023) · Nutrients · doi:10.3390/nu15153365 · Cited by 56
Disruptive physiology: olfaction and the microbiome–gut–brain axis
Bienenstock, J., Kunze, W., & Forsythe, P. (2017) · Biological reviews/Biological reviews of the Cambridge Philosophical Society · doi:10.1111/brv.12348 · Cited by 53
Willing, B. P., & Kessel, A. G. V. (2010) · Livestock Science · doi:10.1016/j.livsci.2010.06.031 · Cited by 52
The microbiome and cognitive aging: a review of mechanisms
Komanduri, M., Gondalia, S. V., Scholey, A. B., & Stough, C. K. K. (2019) · Psychopharmacology · doi:10.1007/s00213-019-05231-1 · Cited by 49
The Role and Mechanism of Intestinal Flora in Blood Pressure Regulation and Hypertension Development
Li, J., Yang, X., Zhou, X., & Cai, J. (2020) · Antioxidants and Redox Signaling · doi:10.1089/ars.2020.8104 · Cited by 51
Gut Microbiota and Pathophysiology of Depressive Disorder
Kunugi, H. (2021) · Annals of Nutrition and Metabolism · doi:10.1159/000518274 · Cited by 53
Kong, C., Li, Z., Mao, Y., Chen, H., Hu, W., Han, B., & Wang, L. (2021) · Food & Function · doi:10.1039/d1fo01836a · Cited by 47
Sashihara, T., Nagata, M., Mori, T., Ikegami, S., Gotoh, M., Okubo, K., Uchida, M., & Itoh, H. (2013) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/apnm-2012-0490 · Cited by 46
Diagnostics and therapeutic implications of gut microbiota alterations in cardiometabolic diseases
Schiattarella, G. G., Sannino, A., Esposito, G., & Perrino, C. (2018) · Trends in Cardiovascular Medicine · doi:10.1016/j.tcm.2018.08.003 · Cited by 47
Bartley, A., Yang, T., Arocha, R., Malphurs, W. L., Larkin, R., Magee, K. L., Vickroy, T. W., & Zubcevic, J. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.01593 · Cited by 44
Inflammatory Stress Effects on Health and Function After Spinal Cord Injury
Noller, C. M., Groah, S. L., & Nash, M. S. (2017) · Topics in Spinal Cord Injury Rehabilitation · doi:10.1310/sci2303-207 · Cited by 42
Munir, M. U., Ali, S. A., Chung, K. H. K., Käkinen, A., Javed, I., & Davis, T. P. (2024) · Gut Microbes · doi:10.1080/19490976.2024.2422468 · Cited by 45
Mörkl, S., Narrath, M., Schlotmann, D., Sallmutter, M.-T., Putz, J., Lang, J., Brandstätter, A., Pilz, R., Lackner, H. K., Goswami, N., et al. (2025) · Gut Microbes · doi:10.1080/19490976.2025.2492377 · Cited by 47
Hesampour, F., Bernstein, C. N., & Ghia, J. (2023) · Inflammatory Bowel Diseases · doi:10.1093/ibd/izad211 · Cited by 38
Hua, H., Huang, C., Liu, H., Xu, X., Xu, X., Wu, Z., Liu, C., Wang, Y. Y., & Yang, C. (2022) · Neuropharmacology · doi:10.1016/j.neuropharm.2022.109272 · Cited by 37
Inflammatory Bowel Disease: Role of Vagus Nerve Stimulation
Fornaro, R., Actis, G. C., Caviglia, G. P., Pitoni, D., & Ribaldone, D. G. (2022) · Journal of Clinical Medicine · doi:10.3390/jcm11195690 · Cited by 38
Ohara, K., Fukuda, T., Ishida, Y., Takahashi, C., Ohya, R., Katayama, M., Uchida, K., Tominaga, M., & Nagai, K. (2017) · Scientific Reports · doi:10.1038/s41598-017-16150-6 · Cited by 34
Self-citationPathophysiological Links Between Obesity and Dementia
Zhang, D. E. W., Tran, V., Vinh, A., Dinh, Q. N., Drummond, G. R., Sobey, C. G., Jelinic, M., & Silva, T. M. D. (2023) · NeuroMolecular Medicine · doi:10.1007/s12017-023-08746-1 · Cited by 36
Matsutomo, T. (2019) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2019.8375 · Cited by 35
The gut-brain axis in Parkinson's disease
Bonaz, B. L. (2023) · Revue Neurologique · doi:10.1016/j.neurol.2023.11.004 · Cited by 34
Swann, J. R., García‐Pérez, I., Braniste, V., Wilson, I. D., Sidaway, J. E., Nicholson, J. K., Pettersson, S., & Holmes, E. C. (2017) · Journal of Pharmaceutical and Biomedical Analysis · doi:10.1016/j.jpba.2017.05.040 · Cited by 31
Parekh, P. J., Nayi, V., Johnson, D. A., & Vinik, A. I. (2016) · Frontiers in Endocrinology · doi:10.3389/fendo.2016.00055 · Cited by 31
Acupuncture influences multiple diseases by regulating gut microbiota
Xu, H., Luo, Y., Li, Q., & Zhu, H. (2024) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2024.1371543 · Cited by 33
Tanida, M., Niijima, A., Shen, J., Yamada, S., Sawai, H., Fukuda, Y., & Nagai, K. (2006) · Experimental Biology and Medicine · doi:10.1177/153537020623101006 · Cited by 30
Self-citationHorii, Y., Kaneda, H., Fujisaki, Y., Fuyuki, R., Nakakita, Y., Shigyo, T., & Nagai, K. (2014) · Journal of Applied Microbiology · doi:10.1111/jam.12435 · Cited by 29
Self-citationHorii, Y., Nakakita, Y., Fujisaki, Y., Yamamoto, S., Itoh, N., Miyazaki, K., Kaneda, H., Oishi, K., Shigyo, T., & Nagai, K. (2013) · Neuroscience Letters · doi:10.1016/j.neulet.2013.01.037 · Cited by 28
Self-citationThe Potential Effects of Radiation on the Gut-Brain Axis
Jones, C. B., Davis, C. M., & Sfanos, K. S. (2020) · Radiation Research · doi:10.1667/rr15493.1 · Cited by 27
Shen, J., Nakamura, H., Fujisaki, Y., Tanida, M., Horii, Y., Fuyuki, R., Takumi, H., Shiraishi, K., Kometani, T., & Nagai, K. (2009) · Neuroscience Letters · doi:10.1016/j.neulet.2009.05.067 · Cited by 28
Self-citationThe Role of Gut Microbiome in Irritable Bowel Syndrome: Implications for Clinical Therapeutics
Zhao, Y., Zhu, S., Dong, Y., Xie, T., Chai, Z., Gao, X., Dai, Y., & Wang, X. (2024) · Biomolecules · doi:10.3390/biom14121643 · Cited by 32
Tanida, M., Imanishi, K., Akashi, H., Kurata, Y., Chonan, O., Naito, E., Kunihiro, S., Kawai, M., Kato-Kataoka, A., & Shibamoto, T. (2013) · Journal of Diabetes Investigation · doi:10.1111/jdi.12141 · Cited by 27
Self-citationEffect of Lactic Acid Bacteria on Lipid Metabolism and Fat Synthesis in Mice Fed a High-fat Diet
Yonejima, Y., Ushida, K., & Yoshiro, M. O. R. I. (2013) · Bioscience of Microbiota Food and Health · doi:10.12938/bmfh.32.51 · Cited by 28
Mörkl, S., Butler, M., & Wagner‐Skacel, J. (2023) · Journal of Affective Disorders Reports · doi:10.1016/j.jadr.2023.100607 · Cited by 26
Lactobacillus rhamnosus strain JB ‐1 reverses restraint stress‐induced gut dysmotility
West, C. L., Wu, R., Wong, A., Stanisz, A. M., Yan, R. R., Min, K. K. H., Pasyk, M., Neufeld, K. M., Karamat, M. I., Foster, J. A., et al. (2016) · Neurogastroenterology & Motility · doi:10.1111/nmo.12903 · Cited by 31
Changes of gut microbiota in patients at different phases of stroke
Cui, W., Xu, L., Huang, L., Tian, Y., Yang, Y., Li, Y., & Yu, Q. (2023) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.14271 · Cited by 25
The Gut Microbiota–Brain Axis Expands Neurologic Function: A Nervous Rapport
Bauer, K. C., Rees, T., & Finlay, B. B. (2019) · BioEssays · doi:10.1002/bies.201800268 · Cited by 26
Vagal Sensory Gut–Brain Pathways That Control Eating—Satiety and Beyond
Méndez‐Hernández, R., Braga, I., Bali, A. P., Yang, M., & de Lartigue, G. (2025) · Comprehensive physiology · doi:10.1002/cph4.70010 · Cited by 24
Ушакова, Г. А., Fedkiv, O., Prykhodko, O., Pierzynowski, S. G., & Kruszewska, D. (2008) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2008.06.010 · Cited by 24
Altered physiology of gastrointestinal vagal afferents following neurotrauma
Blanke, E. N., Holmes, G. M., & Besecker, E. M. (2020) · Neural Regeneration Research · doi:10.4103/1673-5374.290883 · Cited by 26
Potential Therapeutic Effects of Short-Chain Fatty Acids on Chronic Pain
Tang, Y., Du, J., Wu, H., Wang, M., Liu, S., & Tao, F. (2022) · Current Neuropharmacology · doi:10.2174/1570159x20666220927092016 · Cited by 26
Ejtahed, H., Ardeshirlarijani, E., Tabatabaei‐Malazy, O., Tavassol, Z. H., Hasani‐Ranjbar, S., Soroush, A., & Larijani, B. A. (2020) · Journal of Diabetes & Metabolic Disorders · doi:10.1007/s40200-020-00525-0 · Cited by 23
Metadata
- Authors
- Tanida, M., Yamano, T., Maeda, K., Okumura, N., Fukushima, Y., & Nagai, K.
- Affiliations
- Institute for Protein Research, The University of Osaka (JP)
- Corresponding author
- Nagai, Katsuya
- Venue
- Neuroscience Letters
- Publisher
- Elsevier BV
- Published
- 2005-12
- Volume
- 389
- Issue
- 2
- Pages
- 109-114
- ISSN
- 0304-3940 (ISSN-L)
- OpenAlex
- W2002714430
- Cited by
- 159
- References
- 18
- Citations by year
- 2026: 3 · 2025: 12 · 2024: 10 · 2023: 12 · 2022: 12 · 2021: 9 · 2020: 8 · 2019: 8 · 2018: 12 · 2017: 11 · 2016: 7 · 2015: 3 · 2014: 8 · 2013: 10 · 2012: 7
- FWCI
- 8.39
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Neuroscience Letters (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Agricultural and Biological Sciences › Food Science › Probiotics and Fermented Foods
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Heart Rate Variability and Autonomic Control
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Blood Pressure and Hypertension Studies
- Keywords
- probiotics, renal sympathetic nerve activity, blood pressure, histamine H3 receptor, thioperamide, suprachiasmatic nucleus, circadian rhythm, autonomic neurotransmission, gut-brain axis, antihypertensive effect
- MeSH terms
- Adrenergic Fibers, Animals, Blood Pressure, Denervation, Duodenum, Histamine, Histamine Antagonists, Kidney, Lactobacillus, Male, Neural Pathways, Reaction Time, Suprachiasmatic Nucleus, Urethane, Vagus Nerve, Yogurt, Rats, Wistar, Receptors, Histamine H3, Anesthetics, Intravenous, Rats
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review