Nampt/PBEF/Visfatin Regulates Insulin Secretion in β Cells as a Systemic NAD Biosynthetic Enzyme

Transcriptional silencing and longevity protein Sir2 is an NAD-dependent histone deacetylase

Imai, S.-I., Armstrong, C. M., Kaeberlein, M., & Guarente, L. (2000) · Nature · doi:10.1038/35001622 · Cited by 3,510

Cloning and Characterization of the cDNA Encoding a Novel Human pre-B-Cell Colony-enhancing Factor

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The NAD Biosynthesis Pathway Mediated by Nicotinamide Phosphoribosyltransferase Regulates Sir2 Activity in Mammalian Cells

Revollo, J. R., Grimm, A. A., & Imai, S.-I. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m408388200 · Cited by 1,010

NAD+ metabolism in health and disease

Belenky, P. A., Bogan, K. L., & Brenner, C. (2006) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2006.11.006 · Cited by 1,006

Visfatin, an Adipocytokine with Proinflammatory and Immunomodulating Properties

Moschen, A. R., Kaser, A., Enrich, B., Mosheimer, B. A., Theurl, M., Niederegger, H., & Tilg, H. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.178.3.1748 · Cited by 957

Plasma Visfatin Concentrations and Fat Depot–Specific mRNA Expression in Humans

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A phylogenetically conserved NAD + -dependent protein deacetylase activity in the Sir2 protein family

Smith, J. S., Brachmann, C. B., Celic, I., Kenna, M. A., Muhammad, S., Starai, V. J., Avalos, J. L., Escalante-Semerena, J. C., Grubmeyer, C., Wolberger, C., et al. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.12.6658 · Cited by 718

Elevated Plasma Level of Visfatin/Pre-B Cell Colony-Enhancing Factor in Patients with Type 2 Diabetes Mellitus

Chen, M., Chung, F., Chang, D., Tsai, J. C. ‐., Huang, H.-F., Shin, S., & Lee, Y. (2006) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2005-1475 · Cited by 660

Increased dosage of mammalian Sir2 in pancreatic β cells enhances glucose-stimulated insulin secretion in mice

Moynihan, K. A., Grimm, A. A., Plueger, M. M., Bernal‐Mizrachi, E., Ford, E. L., CRAS-MÉNEUR, C. M. H., Permutt, M. A., & Imai, S. (2005) · Cell Metabolism · doi:10.1016/j.cmet.2005.07.001 · Cited by 638

eNAMPT Blockade Disrupts PD-L1/PD-1 Axis to Counter T-Cell Evasion in Breast Cancer

Fischer, A. M., & Weber, J. L. (2024) · Archive of International Journal of Cancer and Allied Science · doi:10.51847/k6aytuxgqa · Cited by 1

NAD+ and Its Precursors for Health and Longevity

Yi, L. (2026) · Healthy ageing and longevity · doi:10.1007/978-3-032-11608-6_5 · Cited by 1

Therapeutic potential of dihydronicotinamide riboside (NRH) on obesity and glucose intolerance in mice

Rumpler, M., van Mierlo, G., Vinten, K. T., Giner, M. P., Christen, S., Hayat, F., Makarov, M. V., Gardeux, V., Russeil, J., Schomakers, B. V., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-70965-4 · Cited by 1

In silico screening of candidate NAMPT modulators for treatment of age-related diseases

Nahálková, J., & Zanchi, F. B. (2026) · In Silico Research in Biomedicine · doi:10.1016/j.insi.2026.100587 · Cited by 1

Regeneration and Aging: Regulation by Sirtuins and the NAD+ Salvage Pathway

Borradaile, N. M., Watson, A., & Pickering, J. G. (2010) · Elsevier eBooks · doi:10.1016/b978-0-12-380928-5.10019-3 · Cited by 3

Nicotinamide Phosphoribosyltransferase Inhibitors

Wu, D., Cheranova, D. I., Daniel, P., Qin, L., & Qing, S. (2012) · InTech eBooks · doi:10.5772/34981 · Cited by 1

NEURO-ADIPOSE INTERACTIONS (BIACTOME). IMPLICATION IN CARDIOMETABOLIC DISEASE

Chaldakov, G. N., Aloe, L., Tonchev, A. B., Chervenkov, T., Fiore, M., & Zhelezov, M. (2014) · Cited by 1

Toward Productive Aging: SIRT1, Systemic NAD Biosynthesis, and the NAD World

Imai, S. (2010) · Cornea · doi:10.1097/ico.0b013e3181ea4714 · Cited by 1

ADIPOCITOQUINAS Y SÍNDROME METABÓLICO: ROL DE LA VISFATINA EN LA PATOGENIA DE ENFERMEDAD CARDIOVASCULAR

Cecilia, M., Lanzi, R., & Miatello, R. M. (2011) · Cited by 1

Pathways Leading to Child Obesity: An Overview

Jarouliya, U., & Keservani, R. K. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-812840-4.00012-8 · Cited by 2

Potential significance of NAD+ biology translational research in super-aged Japan

山口慎太郎, 裕, 伊., & 純, 吉. (2020) · Nippon Ronen Igakkai Zasshi Japanese Journal of Geriatrics · doi:10.3143/geriatrics.57.213 · Cited by 1

Sağlıklı insanlarda uyku yoksunluğunun insülin, resistin ve visfatin düzeylerine etkileri

Gürel, E. E., Ayaz, L., & Öztürk, L. (2022) · Akdeniz Medical Journal · doi:10.53394/akd.1001617 · Cited by 1

Obesity, adipokines and their relationship with insulin resistance

García-Ortega, W. A., Angulo-Camacho, J. Á., & Ibarra-Sánchez, A. (2023) · Ciencia Latina Revista Científica Multidisciplinar · doi:10.37811/cl_rcm.v6i6.4335 · Cited by 1

Pharmacology of NAD+boosters

Braidy, N., & Sachdev, P. S. (2023) · Elsevier eBooks · doi:10.1016/b978-0-12-823679-6.00005-9 · Cited by 1

Investigation of Airway Obstruction Severity Based on Plasma Visfatin Level in Asthmatic Women

Fekri, M. S., Bajgani, S. M. H., Shafiepour, M., Yazdani, R., & Dalfardi, B. (2023) · Current Respiratory Medicine Reviews · doi:10.2174/1573398x19666230315114948 · Cited by 1

Pancreatic Islets as a Target of Adipokines

Reiterer, M., Gilani, A., & Lo, J. C. (2022) · Comprehensive physiology · doi:10.1002/j.2040-4603.2022.tb00238.x · Cited by 1

Blood-Based Novel Biomarkers for Nonalcoholic Steatohepatitis

Qiu, Y., Wang, S., Wan, T., Ye, M., Jiang, R., Pei, L., & Yang, L. (2018) · Biomarkers in Medicine · doi:10.2217/bmm-2017-0361 · Cited by 1

Nampt (Visfatin) Influence on Proliferative Activity of Normal Rat Adrenocortical Cells and Human Adrenal Corticocarcinoma Nci-H295r Cells

Celichowski, P., Jopek, K., Szyszka, M., Milecka, P., Malendowicz, L. K., Tyczewska, M., & Ruciński, M. (2018) · Medical Journal of Cell Biology · doi:10.2478/acb-2018-0007 · Cited by 1

Biomarkers of Insulin Resistance

Cox‐York, K. A., & Pereira, R. I. (2019) · Contemporary Endocrinology · doi:10.1007/978-3-030-25057-7_11 · Cited by 1

Serum Visfatin Levels in Pediatric Hemodialysis Patients: Association with Circulating HDL-Cholesterol

Galal, A., Elshamaa, M. F., Aa, A., Farid, T., Tm, A. E. M., & El-Saaid, G. S. (2011) · Journal für Kardiologie (Krause & Pachernegg GmbH) · Cited by 1

Adipocyte Development and Experimental Obesity

ISGANAITIS, E. M., & Patti, M. (2010) · Endocrine updates · doi:10.1007/978-1-4419-7034-3_16 · Cited by 1

Métabolisme du NAD et contrôle de la réponse inflammatoire

Gool, F. V., Gallí, M., Rongvaux, A., Andris, F., & Léo, O. (2009) · médecine/sciences · doi:10.1051/medsci/2009256-7551 · Cited by 1

Sirtuin Function in Longevity

Smith, D. L., & Smith, J. S. (2009) · Springer eBooks · doi:10.1007/978-90-481-3465-6_6 · Cited by 1

Novel NAD+ metabolomic technologies and their applications to Nicotinamide Riboside interventions

Trammell, S. A. J., Wright, M. E., Piper, R. C., Brenner, C., Slusarski, D. C., & Wilson, M. E. (2016) · doi:10.17077/etd.mk206led · Cited by 1

Caloric restriction overcomes pre-diabetic and hypertension induced by high fat diet and renal artery stenosisPreprint

Faria, M. S. D. S. N., Pimentel, V. E., Helaehil, J. V., Bertolo, M. C., Santos, N. T. H., Silva-Neto, P. V. D., Thomazini, B. F., de Oliveira, C. A., & do Amaral, M. E. C. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.03.30.437684 · Cited by 1

Long-Term NMN Treatment Increases Lifespan and Healthspan in Mice in a Sex Dependent MannerPreprint

Kane, A. E., Chellappa, K., S, M., Arnold, M. W., Li, J., Amorim, J. A., Diener, C., Zhu, D., Mitchell, S. J., Griffin, P. T., et al. (2024) · SSRN Electronic Journal · doi:10.2139/ssrn.4857461 · Cited by 1

Investigation of effect of hyperinsulinaemia on adipose tissue microvasculature.

Bakhamis, A. (2015) · UCL Discovery (University College London)

Adipokines, Inflammation, and Atherosclerosis

Stulnig, T. M., & Zeyda, M. (2011) · Springer eBooks · doi:10.1007/978-3-7091-0338-8_14

Regulation of neutrophil function by NAMPT

Roberts, K. (2013) · doi:10.17638/00008355

Investigating the role of nicotinamide phosphoribosyltransferase (NAMPT) in cartilage catabolism

Evans, L. (2013) · ORCA Online Research @Cardiff (Cardiff University)

Adipocytokines, Oxidative Stress and Impaired Cardiovascular Functions

Zavalza-Gómez, A. B., Islas-Carbajal, M. C., & Snchez, A. R. R. (2012) · InTech eBooks · doi:10.5772/32621 · Cited by 1

Adipokines: Regulators of Lipid Metabolism

Gualillo, O., & Lago, F. (2009) · Springer eBooks · doi:10.1007/978-3-642-00300-4_11

No Association between Visfatin (NAMPT) Gene Variants and Metabolic Traits in the Newfoundland Population

Shea, J. L., Loredo‐Osti, J. C., & Sun, G. (2010) · Genetics & Epigenetics · doi:10.4137/geg.s5337

Effect of rosiglitazone and metformin on serum visfatin level in newly diagnosed patients with type 2 diabetes mellitus

Huang, Y., Zou, J., & Liu, Z. (2010) · Academic Journal of Second Military Medical University · doi:10.3724/sp.j.1008.2010.00564

Visfatin Gene Responses to 8 Weeks of Treadmill Running with or without Pistachio atlantica Liquid Extraction in Female Rat Tissues

Ghanbari–Niaki, A., Zarekookandeh, N., Rahmati-Ahmadabad, S., & Fathi, R. (2012) · Food and Nutrition Sciences · doi:10.4236/fns.2012.38150

Effect of grape polyphenol concentrate "Enoant" on adipokines secretion in experimental metabolic syndrome

Zagayko, A. L., Kravchenko, G. B., & Krasilnikova, O. A. (2012) · Adipobiology · doi:10.14748/adipo.v4.284

The effects of the adipocyte-secreted proteins resistin and visfatin on the pancreatic beta-cell

Onyango, D. (2009) · Wolverhampton Intellectual Repository and E-Theses (University of Wolverhampton)

Strategies to Potentiate the Cellular Poly(ADP-ribosyl)ation Response to DNA Damage

Kunzmann, A. (2009)

Determination of ATP release of human platelets using collagen sepharose resin.

Tatsumi, N., Niri, M., Furukawa, Y., Inoue, T., Sagawa, H., & Yamane, T. (1987) · PubMed

Studio degli intermedi deamidati del NAD e del loro metabolismo

Carradori, M. R. (2014) · Università Politecnica delle Marche (Università Politecnica delle Marche)

The NAMPT-mediated NAD salvage pathway in cancer cell metabolism and its regulation by resveratrol

Schuster, S. (2015) · Qucosa (Saxon State and University Library Dresden)

Up-to-Date on Novel “Adipocrines”

Carpéné, C., & Saulnier‐Blache, J. S. (2012) · Springer eBooks · doi:10.1007/978-2-8178-0343-2_15

Recent advances on the relationship between visfatin and type 2 diabetes mellitus

Jian, Z., Yun-chao, S., & Li-ling, W. (2009) · Xiandai shengwu yixue jinzhan

The effect of high-intensity intermittent exercise and carbohydrate supplementation on plasma visfatin

Mellick, P. F. (2013)

THE EFFECTS OF ACUTE ENDURANCE EXERCISE ON VISFATIN AND INSULIN LEVELS IN OBESE WOMEN

Taghian, F., & Maryam, Z. (2014)

Characteristics of serum Nampt and its relationship with TNFα in patients with type 2 diabetes mellitus

He, M., Zhao, J., Li, Y., Liu, Q., Xie, Z., & Zhang, X. (2010) · Academic Journal of Second Military Medical University · doi:10.3724/sp.j.1008.2010.01038

Pharmacogenetics of Oral Antidiabetic Drugs: Potential Clinical Application

Yin, J., & Yu, G. (2012) · Endocrinology & Metabolic Syndrome · doi:10.4172/2161-1017.s5-003

Effect of intermittent and continuous exercise in water and land on Visfatin in pre and post menopausal obese women

Gaeini, A. A., Payamipoor, S., Satarifard, S., & Kordi, M. R. (2015) · Bimonthly Journal of Hormozgan University of Medical Sciences

NAD + -Dependent Deacetylases and Medical Therapy

Kumar, A., Ben-Aderet, L., Elayyan, J., & Dvir‐Ginzberg, M. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-803239-8.00035-1

A Role of Visceral Adipose and Gastric Tissue in Inflammatory Conditions Associated With Metabolic Syndrome

Mehta, R. (2013) · doi:10.13021/mars/7304

Clinical Implications of Pharmacogenetic Data

Chiara, G. (2012)

Omentin and subclinical cardiovascular disease in rheumatoid arthritis

Robinson, C. (2016)

The Neuroprotective Compound P7C3-A20 Promotes Neurogenesis and Improves Functional Outcomes After Focal Cerebral Ischemia

Loris, Z. B. (2017)

Vitamin B3 salvage and NAD\(^+\) metabolism in skeletal muscle

Fletcher, R. S. (2017) · University of Birmingham Institutional Research Archive (University of Birmingham)

Tubuloglomerular Communication in Diabetic Nephropathy

Wakino, S., Hasegawa, K., & Itoh, H. (2018) · Springer eBooks · doi:10.1007/978-3-319-93521-8_14

Nicotinamide Mononucleotide in the Context of Elevated Plasma Levels of Free Fatty Acids Improves Glucose Tolerance by Decreasing Insulin Clearance

Nahle, A. (2016) · TSpace (University of Toronto)

The importance of pharmacological modulation of the enzymatic activity of CD38 and intracellular NAD levels

Al-Abady, Z. N., Jabbar, N. K., & Alfarhani, B. F. (2019) · Journal of Physics Conference Series · doi:10.1088/1742-6596/1294/5/052073 · Cited by 1

Understanding the Molecular Pathogenesis of Retinal Neurodegeneration

Lin, J. B. (2020) · Open Scholarship Institutional Repository (Washington University in St. Louis) · doi:10.7936/v6tn-2v15

Caloric Restriction Overcomes Pre-Diabetic and Hypertension Induced by High Fat Diet and Renal Artery StenosisPreprint

Faria, M. S. D. S. N., Pimentel, V. E., Helaehil, J. V., Bertolo, M. C., Santos, N. T. H., Silva-Neto, P. V. D., Thomazini, B. F., de Oliveira, C. A., & do Amaral, M. E. C. (2021) · Research Square · doi:10.21203/rs.3.rs-1085770/v1

Inflammatory Pathways Linked to β Cell Demise in Diabetes

Imai, Y., Morris, M. A., Dobrian, A. D., Taylor, D., & Nadler, J. L. (2014) · Springer eBooks · doi:10.1007/978-94-007-6686-0_30

Hormonal regulation of visfatin and adiponectin system in quail muscle cells

Ramser, A., & Dridi, S. (2023) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/j.cbpa.2023.111425

The Correlation between Adipokines and Gynecological Diseases

祁, 璘. (2023) · Advances in Clinical Medicine · doi:10.12677/acm.2023.1361317

Chemerin, Visfatin, Omentin-1 and Their Gene Polymorphisms Associated With Diabetes Associated Chronic Kidney DiseasePreprint

Ahmed, C. M. J., Vasanthan, M., Vinodhini, V. M., & Renuka, P. (2024) · Research Square · doi:10.21203/rs.3.rs-4739209/v1

NRH, a potent NAD+ booster, improves glucose homeostasis and lipid metabolism in diet-induced obese mice though an active adenosine kinase pathwayPreprint

Zeng, X., Wang, Y., Farias, K., Rappa, A., Darko, C., Sauve, A. A., & Yang, Y. J. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.08.29.610289

Significance of Adipose Tissue as an Endocrine Organ

Avtanski, D. B., & Stojchevski, R. (2024) · Contemporary Endocrinology · doi:10.1007/978-3-031-72570-8_1

Alterations in serum concentrations of visfatin and betatrophin in dogs with diabetes mellitus

Slon, A., & Mazaki‐Tovi, M. (2025) · Domestic Animal Endocrinology · doi:10.1016/j.domaniend.2025.106914

NAMPT activity plays a key role in driving autoimmune processes that characterise type 1 diabetes development in micePreprint

Egbase, D., Sayers, S. R., Haq, N., Varghese, J. J., Gesheva, V., Bhattacharya, S., Kynaston, J., Hubber, E.-L., Smith, L. I. F., Pullen, T. J., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.01.14.632985

CNS Targets of Adipokines

Beall, C., Hanna, L., & Ellacott, K. L. J. (2017) · Comprehensive physiology · doi:10.1002/j.2040-4603.2017.tb00781.x

In silico screening of candidate NAMPT modulators for treatment of age-related diseasesPreprint

Nahálková, J., & Zanchi, F. B. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.04.07.647561

NAMPT-mediated deacetylation of HCLS1 protein promotes clonogenic growth of pediatric CML cells

Samareh, B., Klimenkova, O., Aghaallaei, N., Cheng, L., Zikic, A., Loghmani, H., Tesakov, I. P., Müller, P., Suttorp, M., Welte, K., et al. (2025) · Experimental Hematology · doi:10.1016/j.exphem.2025.104801

NAD+ metabolism as a target for anti-aging

Uchida, H., & Nakagawa, T. (2025) · Folia Pharmacologica Japonica · doi:10.1254/fpj.24072

Keeping up with the nicotinamides: NADP(H), the forgotten circadian cofactor that keeps metabolic time

Palluth, L., Takahashi, J. S., & Green, C. B. (2025) · Life Metabolism · doi:10.1093/lifemeta/loaf034 · Cited by 2

Adipose Tissue Overexpression of Nicotinamide Phosphoribosyltransferase Prevents Metabolic Dysfunction in Obese MicePreprint

Ferguson, D., Gadson, E. I., Markan, K. R., Yoshino, J., Lin, M., Habibi, M., Tiash, S., Cui, X., Kouranova, E. V., Franczak, E., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.09.30.679563

Targeting NAD + Salvage Suppresses PBMC Inflammation to Improve Cognitive Function in Vascular Cognitive Impairment

Li, Z., Zhang, H., Feng, R., Qi, W., Wang, Y.-T., Li, Q., & Zhang, K. (2025) · Stroke · doi:10.1161/strokeaha.125.052431

Role of visfatin on early embryogenesis in normal weight and obese mice. Studies on siRNA induced knockdown model

Kurowska, P., Honda, S., Tanaka, G., Yuwei, G., Minami, N., Rak, A., & Ikeda, S. (2025) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2025.112702

FGF2 Enhances MSCs Secretome Therapy for Skin Photoaging by Delaying Senescence via iNAMPT/AMPK Signaling and Facilitating eNAMPT-Mediated Regenerative Crosstalk

Zhang, Y., Lu, M., Ouyang, J., Liang, L., Li, F., Pei, Z., Chen, L., Ye, M., Tan, J., Xiang, L., et al. (2025) · Stem Cell Reviews and Reports · doi:10.1007/s12015-025-11018-z

Additional file 1 of Zebrafish nampt-a mutants are viable despite perturbed primitive hematopoiesis

Pomreinke, A. P., & Müller, P. (2024) · Figshare · doi:10.6084/m9.figshare.26713807

Exploring NAD(+) metabolism in host-pathogen interactions

Belinha, A., Gaifem, J., Mesquita, I., & Silvestre, R. (2016) · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT)

Exploring novel pathways and potential therapeutic targets for diabetic nephropathy: The interplay of podocytes and proximal tubular epithelial cells

Abdelaziz, T. S. (2026) · World Journal of Diabetes · doi:10.4239/wjd.v17.i1.114082

Possible Involvement of NAMPT in the Anti-Obesity Effect of Oral Administration of Fermented Rice with Lactobacillus kefiranofaciens (Rice Kefiran) in C57BL/6J Mice

Othman, M. B., & Sakamoto, K. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27041912

Activité ambivalente du nicotinamide chez le parasite Leishmania : adjuvant thérapeutique dans le traitement des leishmanioses et précurseur majeur du NAD+ chez le parasite.

Gazanion, É. (2010) · theses.fr (ABES) · doi:10.70675/5d636192z8a90z4ee8z89d1ze397f3b1e02d

Adaptation de fonction et de masse des cellules bêta pancréatiques dans un modèle d'insulinorésistance induite par les glucocorticoïdes.

Courty, É. (2018) · theses.fr (ABES) · doi:10.70675/e3b505daz4530z48a2z927bz483fbf05e110

Pyrimidine and NAD salvage pathways : unexpected allies in the maintenance of genome stability

Silveira, S. C. (2018) · theses.fr (ABES) · doi:10.70675/d8951764z7ae2z4d5eza2e1z0b24bea9f901

Etude de trois adipocytokines, adiponectine, visfatine et chémérine au niveau plasmatique et dans plusieurs tissus métaboliques et reproducteurs de différentes espèces

Mellouk, N. (2018) · doi:10.70675/f6ee516az0355z4eb7za779z694d7dd94b98

Effets de l’exercice et d’une modulation du métabolisme du NAD sur la fonction cardiaque et musculaire dans la cardiomyopathie dilatée

Deloux, R. (2018) · theses.fr (ABES) · doi:10.70675/187a7874z7c88z4ab7z9392zc08078be5b17

Expression de quatre adipocytokines, chémérine, adiponectine, visfatine et adipoline au niveau plasmatique et dans les tissus métaboliques et reproducteurs chez les truies Large White et Meishan et en réponse à diverses conditions nutritionnelles chez la poule reproductrice

Barbe, A. (2020) · theses.fr (ABES) · doi:10.70675/a1929a18zc99dz4f74zb8f8z614bf9e123e9

Finishing Barrow Skeletal Muscle Performance and Fatigue Response to Large-Dose Nicotinamide Riboside Supplementation

Alambarrio, D. A., Li, X., Zedonek, S. S., Willis, S. E., Proctor, J. N., Mozafari, F., Call, J. A., Delgado, L. E., Doran, M. S., & Gonzalez, J. M. (2026) · Metabolites · doi:10.3390/metabo16040261

Adipose-Derived Proinflammatory Visfatin Promotes Vascular Calcification via TLR4 and is Suppressed by Empagliflozin

Zhang, Y., Zhao, Y., Luo, Y., Wang, L., Liao, J., Lu, H., Zhang, X., & Ji, X. (2026) · Inflammation · doi:10.1007/s10753-026-02507-5 · Cited by 1

Targeting the mitochondrial thermogenesis pathway for neuroprotection in neonatal hypoxic-ischemic encephalopathy by curcumin

Wang, X., Zhang, B., Eide, S., Zhang, X.-Y., Yang, M., Feng, Z.-P., & Sun, H. (2026) · Acta Pharmacologica Sinica · doi:10.1038/s41401-026-01813-w

Investigation of the reactions between NAD+ and a photoactivatable anticancer Pt(IV) prodrug by ESI-MS

Hu, Y., Zhang, J., Lin, J., Wu, X., Wu, K., & Wang, F. (2026) · Microchemical Journal · doi:10.1016/j.microc.2026.118537

NAMPT activity plays a key role in driving autoimmune processes that mediate beta-cell death and type 1 diabetes development in mice

Egbase, D., Sayers, S. R., Haq, N., Gesheva, V., Varghese, J. J., Bhattacharya, S., Kynaston, J., Hubber, E.-L., Smith, L. I. F., Pullen, T. J., et al. (2026) · Cell Death and Disease · doi:10.1038/s41419-026-08700-6

КЛІНІЧНЕ ЗНАЧЕННЯ ВІСФАТИНУ ЯК АДИПОЦИТОКІНОВОГО БІОМАРКЕРА У ЖІНОК ІЗ ПАТОЛОГІЄЮ ЕНДОМЕТРІЯ, АСОЦІЙОВАНОЮ З ОЖИРІННЯМ

Marichereda, V., & Drobot, D. I. (2026) · Актуальні питання педіатрії акушерства та гінекології · doi:10.11603/24116-4944.2026.1.16380

Sirtuin modulators: small molecules and natural compounds

Dubey, R., & Prabhakar, P. K. (2026) · Elsevier eBooks · doi:10.1016/b978-0-443-45380-9.00004-3

Adipose Tissue Overexpression of Nicotinamide Phosphoribosyltransferase Prevents Metabolic Dysfunction in Obese Mice via Extracellular Vesicles

Ferguson, D., Gadson, E. I., Markan, K. R., Yoshino, J., Palacios, H. H., Lin, M., Habibi, M., Tiash, S., Cui, X., Kouranova, E. V., et al. (2026) · Diabetes · doi:10.2337/db25-0914

NAMPT activation uncovers a senescence-specific vulnerability and promotes healthy aging in combination with NAMPreprint

Alcaraz, M., Ramachandra, R., Arnold, R., Teneche, M. G., Rajesh, A., Haddadin, L., Taing, M., Lei, X., Gandhi, A., Tzaridis, T., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.08.06.743365 · Cited by 1

Evaluation of visfatin levels in patients with hyperemesis gravidarum

Şanlı, C., Fener, H., Ayyıldız, H., Halisçelik, M. A., & Kalaycı, M. Z. (2026) · Scandinavian Journal of Clinical and Laboratory Investigation · doi:10.1080/00365513.2026.2713139

Tyrosine phosphorylation and dimerization cooperatively activate NAMPT to enable NAD+ synthesis in cancerPreprint

Basappa, J., Lobello, C., Faustino, A. M., Uribe‐Alvarez, C., Rushmore, D., Sen, N., Wang, L., Efimov, A., Cai, K. Q., Schneider, J. L., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.08.13.744642

The role of exercise in modulating NAD+ metabolic enzymes: mechanisms and health benefits

Anas, Sundus, H., Khan, S. A., Ahmed, S. S., Muruganantham, P., & Madar, I. H. (2026) · Frontiers in Sports and Active Living · doi:10.3389/fspor.2026.1863337

eNAMPT-IFITM3 axis links neuroinflammation to γ-secretase activation

Hyun, J., Jung, S., Noh, Y., Cho, Y., Saido, T. C., Nah, J., Kim, K. W., & Jung, Y. (2026) · iScience · doi:10.1016/j.isci.2026.117496

Mechanism of the NAMPT-SIRT2-Lactate Axis in Senescence of Human Nucleus Pulposus Cells

Zhang, W., Mo, L., Guo, H., 张西兵, Tang, H., Li, W., & Liu, C. (2026) · Frontiers in Bioscience-Landmark · doi:10.31083/fbl51724

Nampt/PBEF/Visfatin: A New Player in β Cell Physiology and in Metabolic Diseases?

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The regulation of nicotinamide adenine dinucleotide biosynthesis by Nampt/PBEF/visfatin in mammals

Revollo, J. R., Grimm, A. A., & Imai, S. (2007) · Current Opinion in Gastroenterology · doi:10.1097/mog.0b013e32801b3c8f · Cited by 316

Progress in functional research of nicotinamide phosphoribosyltransferase

He-li, D. (2009) · International Journal of Internal Medicine

Nampt: linking NAD biology, metabolism and cancer

Garten, A., Petzold-Quinque, S., Körner, A., Imai, S., & Kieß, W. (2008) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2008.10.004 · Cited by 399

Expression and Regulation of Nampt in Human Islets

Kover, K. L., Tong, P. Y., Watkins, D. J., Clements, M. A., Stehno‐Bittel, L., Novikova, L., Bittel, D., Kibiryeva, N., Stuhlsatz, J., Yan, Y., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0058767 · Cited by 47