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Increased Endothelial Tetrahydrobiopterin Synthesis by Targeted Transgenic GTP-Cyclohydrolase I Overexpression Reduces Endothelial Dysfunction and Atherosclerosis in ApoE-Knockout Mice
Open accessAbstract
Objective— Increased production of reactive oxygen species and loss of endothelial nitric oxide (NO) bioactivity are key features of vascular disease states such as atherosclerosis. Tetrahydrobiopterin (BH4) is a required cofactor for NO synthesis by endothelial nitric oxide synthase (eNOS); pharmacologic studies suggest that reduced BH4 availability may be an important mediator of endothelial dysfunction in atherosclerosis. We aimed to investigate the importance of endothelial BH4 availability in atherosclerosis using a transgenic mouse model with endothelial-targeted overexpression of the rate-limiting enzyme in BH4 synthesis, GTP-cyclohydrolase I (GTPCH). Methods and Results— Transgenic mice were crossed into an ApoE knockout (ApoE-KO) background and fed a high-fat diet for 16 weeks. Compared with ApoE-KO controls, transgenic mice (ApoE-KO/GCH-Tg) had higher aortic BH4 levels, reduced endothelial superoxide production and eNOS uncoupling, increased cGMP levels, and preserved NO-mediated endothelium dependent vasorelaxations. Furthermore, aortic root atherosclerotic plaque was significantly reduced in ApoE-KO/GCH-Tg mice compared with ApoE-KO controls. Conclusions— These findings indicate that BH4 availability is a critical determinant of eNOS regulation in atherosclerosis and is a rational therapeutic target to restore NO-mediated endothelial function and reduce disease progression.
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“Overexpression of GCH1 in cells and mouse models improves eNOS function (19, 143).”
From Sources of Vascular Nitric Oxide and Reactive Oxygen Species and Their Regulation (2019) · cites this paper as [19]
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Cites
Endothelial dysfunction in cardiovascular diseases: the role of oxidant stress
Cai, H., & Harrison, D. G. (2000) · Circulation Research · doi:10.1161/01.res.87.10.840 · Cited by 3,839
Landmesser, U., Dikalov, S., Price, S. R., McCann, L., Fukai, T., Holland, S. M., Mitch, W. E., & Harrison, D. G. (2003) · Journal of Clinical Investigation · doi:10.1172/jci200314172 · Cited by 1,660
Landmesser, U., Dikalov, S., Price, S. R., McCann, L. A., Fukai, T., Holland, S. M., Mitch, W. E., & Harrison, D. G. (2003) · Journal of Clinical Investigation · doi:10.1172/jci14172 · Cited by 1,652
Mechanisms Underlying Endothelial Dysfunction in Diabetes Mellitus
Hink, U., Li, H., Mollnau, H., Oelze, M., Matheis, E., Hartmann, M., Skatchkov, M. P., Thaiss, F., Stahl, R. A. K., Warnholtz, A., et al. (2001) · Circulation Research · doi:10.1161/01.res.88.2.e14 · Cited by 1,191
Mechanisms of Increased Vascular Superoxide Production in Human Diabetes Mellitus
Guzik, T. J., Mussa, S., Gastaldi, D., Sadowski, J., Ratnatunga, C., Pillai, R. G., & Channon, K. M. (2002) · Circulation · doi:10.1161/01.cir.0000012748.58444.08 · Cited by 979
Self-citationPiedrahita, J. A., Zhang, S. H., Hagaman, J. R., Oliver, P. M., & Maeda, N. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.10.4471 · Cited by 944
Laursen, J. B., Somers, M., Kurz, S., McCann, L., Warnholtz, A., Freeman, B. A., Tarpey, M., Fukai, T., & Harrison, D. G. (2001) · Circulation · doi:10.1161/01.cir.103.9.1282 · Cited by 721
Interactions of Peroxynitrite, Tetrahydrobiopterin, Ascorbic Acid, and Thiols
Kuzkaya, N., Weissmann, N., Harrison, D. G., & Dikalov, S. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m302227200 · Cited by 692
Tetrahydrobiopterin restores endothelial function in hypercholesterolemia.
Stroes, E. S. G., Kastelein, J. J. P., Cosentino, F., Erkelens, W. D., Wever, R. M. F., Koomans, H. A., Lüscher, T. F., & Rabelink, T. J. (1997) · Journal of Clinical Investigation · doi:10.1172/jci119131 · Cited by 588
Oxidation of Tetrahydrobiopterin by Peroxynitrite: Implications for Vascular Endothelial Function
Milstien, S., & Katušić, Z. S. (1999) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1999.1422 · Cited by 492
Research works printed but not linked: 10
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Oxidative Stress in Atherosclerosis
Kattoor, A. J., Pothineni, N. V. K., Palagiri, D. R., & Mehta, J. L. (2017) · Current Atherosclerosis Reports · doi:10.1007/s11883-017-0678-6 · Cited by 1,309
Nitric oxide signalling in cardiovascular health and disease
Farah, C., Michel, L. Y. M., & Balligand, J.-L. (2018) · Nature Reviews Cardiology · doi:10.1038/nrcardio.2017.224 · Cited by 779
Endothelial cell superoxide generation: regulation and relevance for cardiovascular pathophysiology
Li, J.-M., & Shah, A. M. (2004) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00124.2004 · Cited by 773
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Sugamura, K., & Keaney (2011) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2011.05.004 · Cited by 769
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Li, H., Horke, S., & Förstermann, U. (2014) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2014.09.001 · Cited by 678
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Marchio, P., Guerra‐Ojeda, S., Vila, J. M., Aldasoro, M., Víctor, V. M., & Mauricio, M. D. (2019) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2019/8563845 · Cited by 651
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Münzel, T. F., Camici, G. G., Maack, C., Bonetti, N. R., Fuster, V., & Kovacic, J. C. (2017) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2017.05.035 · Cited by 642
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Tejero, J., Shiva, S., & Gladwin, M. T. (2019) · Physiological Reviews · doi:10.1152/physrev.00036.2017 · Cited by 541
NADPH oxidases and oxidase crosstalk in cardiovascular diseases: novel therapeutic targets
Zhang, Y., Murugesan, P., Huang, K., & Cai, H. “. (2019) · Nature Reviews Cardiology · doi:10.1038/s41569-019-0260-8 · Cited by 551
Oxidative stress and endothelial dysfunction in hypertension
Schulz, E., Gori, T., & Münzel, T. F. (2011) · Hypertension Research · doi:10.1038/hr.2011.39 · Cited by 516
Tetrahydrobiopterin: biochemistry and pathophysiology
Werner, E. R., Blau, N., & Thöny, B. (2011) · Biochemical Journal · doi:10.1042/bj20110293 · Cited by 493
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Hopkins, P. N. (2013) · Physiological Reviews · doi:10.1152/physrev.00004.2012 · Cited by 469
Oxidative Stress-Induced Endothelial Dysfunction in Cardiovascular Diseases
Shaito, A. A., Aramouni, K., Assaf, R., Parenti, A., Orekhov, A. N., EL‐Yazbi, A. F., Pintus, G., & Eid, A. H. (2022) · Frontiers in Bioscience-Landmark · doi:10.31083/j.fbl2703105 · Cited by 449
THE REGULATION AND PHARMACOLOGY OF ENDOTHELIAL NITRIC OXIDE SYNTHASE
Dudzinski, D. M., Igarashi, J., Greif, D. M., & Michel, T. M. (2005) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pharmtox.44.101802.121844 · Cited by 425
Thum, T., Fraccarollo, D., Schultheiß, M., Froese, S., Galuppo, P., Widder, J. D., Tsikas, D., Ertl, G., & Bauersachs, J. K. (2007) · Diabetes · doi:10.2337/db06-0699 · Cited by 416
Thomas, S. R., Witting, P. K., & Drummond, G. R. (2008) · Antioxidants & Redox Signaling · doi:10.1089/ars.2008.2027 · Cited by 383
Kim, F., Pham, M., Maloney, E., Rizzo, N. O., Morton, G. J., Wisse, B. E., Kirk, E. A., Chait, A., & Schwartz, M. W. (2008) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.108.169722 · Cited by 364
Endothelial Dysfunction: Is There a Hyperglycemia-Induced Imbalance of NOX and NOS?
Meza, C. A., La Favor, J. D., Kim, D.-H., & Hickner, R. C. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20153775 · Cited by 323
Oxidative stress in vascular disease and its pharmacological prevention
Li, H., Horke, S., & Förstermann, U. (2013) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2013.03.007 · Cited by 321
eNOS Uncoupling in Cardiovascular Diseases - the Role of Oxidative Stress and Inflammation
Karbach, S., Wenzel, P., Waisman, A., Munzel, T., & Daiber, A. (2014) · Current Pharmaceutical Design · doi:10.2174/13816128113196660748 · Cited by 307
Uncoupling of endothelial NO synthase in atherosclerosis and vascular disease
Li, H., & Förstermann, U. (2013) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2013.01.006 · Cited by 285
Sukhanov, S., Higashi, Y., Shai, S., Vaughn, C., Mohler, J., Li, Y., Song, Y., Titterington, J. S., & Delafontaine, P. (2007) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.107.156257 · Cited by 273
Sickle cell disease vasculopathy: A state of nitric oxide resistance
Wood, K. C., Hsu, L. L.-Y., & Gladwin, M. T. (2008) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2008.01.008 · Cited by 252
Endothelial Arginase II: A Novel Target for the Treatment of Atherosclerosis
Ryoo, S., Gupta, G., Benjo, A., Lim, H. K., Camara, A., Sikka, G., Lim, H. K., Sohi, J., Santhanam, L., Soucy, K., et al. (2008) · Circulation Research · doi:10.1161/circresaha.107.169573 · Cited by 236
Self-citationReversal of Cardiac Hypertrophy and Fibrosis From Pressure Overload by Tetrahydrobiopterin
Moens, A. L., Takimoto, E., Tocchetti, C. G., Chakir, K., Bedja, D., Cormaci, G., Ketner, E., Majmudar, M. D., Gabrielson, K., Halushka, M. K., et al. (2008) · Circulation · doi:10.1161/circulationaha.107.737031 · Cited by 237
Self-citationTetrahydrobiopterin in Cardiovascular Health and Disease
Bendall, J. K., Douglas, G., McNeill, E., Channon, K. M., & Crabtree, M. J. (2014) · Antioxidants & Redox Signaling · doi:10.1089/ars.2013.5566 · Cited by 231
Self-citationRedox signaling in cardiovascular health and disease
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Synthesis and recycling of tetrahydrobiopterin in endothelial function and vascular disease
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Self-citationKietadisorn, R., Juni, R. P., & Moens, A. L. (2011) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00540.2011 · Cited by 221
Oxidative risk for atherothrombotic cardiovascular disease
Leopold, J. A., & Loscalzo, J. (2009) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2009.09.009 · Cited by 218
Molecular mechanisms of the cardiovascular protective effects of polyphenols
Andriantsitohaina, R., Auger, C., Chataigneau, T., Étienne-Selloum, N., Li, H., Martínez, M. C., Schini‐Kerth, V. B., & Laher, I. (2012) · British Journal Of Nutrition · doi:10.1017/s0007114512003406 · Cited by 224
Crabtree, M. J., Tatham, A. L., Hale, A. B., Alp, N. J., & Channon, K. M. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.041483 · Cited by 210
Self-citationBendall, J. K., Alp, N. J., Warrick, N., Cai, S., Adlam, D., Rockett, K. A., Yokoyama, M., Kawashima, S., & Channon, K. M. (2005) · Circulation Research · doi:10.1161/01.res.0000187447.03525.72 · Cited by 209
Self-citationResveratrol and Vascular Function
Li, H., Xia, N., Hasselwander, S., & Daiber, A. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20092155 · Cited by 212
Crabtree, M. J., Tatham, A. L., Al-Wakeel, Y., Warrick, N., Hale, A. B., Cai, S., Channon, K. M., & Alp, N. J. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m805403200 · Cited by 200
Self-citationMechanisms for the role of tetrahydrobiopterin in endothelial function and vascular disease
Schmidt, T. S., & Alp, N. J. (2007) · Clinical Science · doi:10.1042/cs20070108 · Cited by 195
Self-citationChannon, K. M. (2004) · Trends in Cardiovascular Medicine · doi:10.1016/j.tcm.2004.10.003 · Cited by 196
Self-citationXu, J., Wu, Y., Song, P., Zhang, M., Wang, S., & Zou, M. (2007) · Circulation · doi:10.1161/circulationaha.106.684795 · Cited by 193
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Moens, A. L., & Kass, D. A. (2006) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/01.atv.0000243924.00970.cb · Cited by 194
Recent Advances in Understanding Endothelial Dysfunction in Atherosclerosis
Yang, Z., & Ming, X. (2006) · Clinical Medicine & Research · doi:10.3121/cmr.4.1.53 · Cited by 191
Resveratrol Reverses Endothelial Nitric-Oxide Synthase Uncoupling in Apolipoprotein E Knockout Mice
Xia, N., Daiber, A., Habermeier, A., Closs, E. I., Thum, T., Spanier, G., Lü, Q., Oelze, M. W., Torzewski, M., Lackner, K. J., et al. (2010) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.110.168724 · Cited by 186
Eskurza, I., Myerburgh, L. A., Kahn, Z. D., & Seals, D. R. (2005) · The Journal of Physiology · doi:10.1113/jphysiol.2005.092734 · Cited by 175
The eNOS signalosome and its link to endothelial dysfunction
Siragusa, M., & Fleming, I. (2016) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-016-1839-0 · Cited by 180
SICKLE CELL DISEASE: ROLE OF REACTIVE OXYGEN AND NITROGEN METABOLITES
Wood, K. C., & Granger, D. N. (2007) · Clinical and Experimental Pharmacology and Physiology · doi:10.1111/j.1440-1681.2007.04639.x · Cited by 164
Cunnington, C., Van Assche, T., Shirodaria, C., Kylintireas, I., Lindsay, A. C., Lee, J. M., Antoniades, C., Margaritis, M., Lee, R., Cerrato, R., et al. (2012) · Circulation · doi:10.1161/circulationaha.111.038919 · Cited by 166
Self-citationResveratrol and Endothelial Nitric Oxide
Xia, N., Förstermann, U., & Li, H. (2014) · Molecules · doi:10.3390/molecules191016102 · Cited by 170
CAI, S., Khoo, J., & Channon, K. M. (2004) · Cardiovascular Research · doi:10.1016/j.cardiores.2004.10.040 · Cited by 164
Self-citationFree radical biology of the cardiovascular system
Chen, A. F., Chen, D., Daiber, A., Faraci, F. M., Li, H., Rembold, C. M., & Laher, I. (2012) · Clinical Science · doi:10.1042/cs20110562 · Cited by 155
Oxidative Stress and Antioxidants in Atherosclerosis Development and Treatment
Poznyak, A. V., Grechko, A. V., Orekhova, V. A., Chegodaev, Y. S., Wu, W., & Orekhov, A. N. (2020) · Biology · doi:10.3390/biology9030060 · Cited by 188
Prevention of Atherosclerosis by Interference with the Vascular Nitric Oxide System
Li, H., & Förstermann, U. (2009) · Current Pharmaceutical Design · doi:10.2174/138161209789058002 · Cited by 154
The clinical significance of endothelial dysfunction
Landmesser, U., & Drexler, H. (2005) · Current Opinion in Cardiology · doi:10.1097/01.hco.0000179821.11071.79 · Cited by 142
Vascular protection by tetrahydrobiopterin: progress and therapeutic prospects
Katušić, Z. S., d’Uscio, L. V., & Nath, K. A. (2008) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2008.10.003 · Cited by 144
Bevers, L. M., Braam, B. G., Post, J. A., van Zonneveld, A. J., Rabelink, T. J., Koomans, H. A., Verhaar, M. C., & Joles, J. A. (2005) · Hypertension · doi:10.1161/01.hyp.0000196735.85398.0e · Cited by 130
Nitric oxide signalling in the regulation of cardiovascular and platelet function
Gkaliagkousi, Ε. (2010) · Frontiers in bioscience · doi:10.2741/3828 · Cited by 124
Moens, A. L., Champion, H. C., Claeys, M. J., Tavazzi, B., Kaminski, P. M., Wolin, M. S., Borgonjon, D. J., Nassauw, L. V., Haile, A., Zviman, M. M., et al. (2008) · Circulation · doi:10.1161/circulationaha.107.725481 · Cited by 119
Role of Uncoupled Endothelial Nitric Oxide Synthase in Abdominal Aortic Aneurysm Formation
Gao, L., Siu, K. L., Chalupský, K., Nguyen, A. H., Chen, P., Weintraub, N. L., Galis, Z. S., & Cai, H. “. (2011) · Hypertension · doi:10.1161/hypertensionaha.111.181644 · Cited by 118
Kossmann, S., Hu, H., Steven, S., Schönfelder, T., Fraccarollo, D., Mikhed, Y., Brähler, M., Knorr, M., Brandt, M., Karbach, S. H., et al. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.604231 · Cited by 116
Interleukin-1 Regulates Multiple Atherogenic Mechanisms in Response to Fat Feeding
Chamberlain, J., Francis, S., Brookes, Z. L. S., Shaw, G., Graham, D., Alp, N. J., Dower, S., & Crossman, D. C. (2009) · PLoS ONE · doi:10.1371/journal.pone.0005073 · Cited by 121
Self-citationMusicki, B., Liu, T., Lagoda, G. A., Strong, T. D., Sezen, S. F., Johnson, J. M., & Burnett, A. L. “. (2010) · The Journal of Sexual Medicine · doi:10.1111/j.1743-6109.2010.01880.x · Cited by 114
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Wu, Y., Ding, Y., Ramprasath, T., & Zou, M. (2020) · Antioxidants and Redox Signaling · doi:10.1089/ars.2020.8112 · Cited by 116
Wang, S., Xu, J., Song, P., Wu, Y., Zhang, J., Choi, H. C., & Zou, M. (2008) · Hypertension · doi:10.1161/hypertensionaha.108.112094 · Cited by 110
M2 Macrophage Polarization Mediates Anti-inflammatory Effects of Endothelial Nitric Oxide Signaling
Lee, W. J., Tateya, S., Cheng, A. M., Rizzo, N. O., Wang, N. F., Handa, P., Wilson, C. L., Clowes, A. W., Sweet, I. R., Bomsztyk, K., et al. (2015) · Diabetes · doi:10.2337/db14-1668 · Cited by 109
Du, Y., Guan, Y., Alp, N. J., Channon, K. M., & Chen, A. F. (2008) · Circulation · doi:10.1161/circulationaha.107.748236 · Cited by 107
Self-citationIwata, N. G., Pham, M., Rizzo, N. O., Cheng, A. M., Maloney, E. J., & Kim, F. (2011) · PLoS ONE · doi:10.1371/journal.pone.0029600 · Cited by 103
A Specific Role for eNOS-Derived Reactive Oxygen Species in Atherosclerosis Progression
Takaya, T., Hirata, K., Yamashita, T., Shinohara, M., Sasaki, N., Inoue, N., Yada, T., Goto, M., Fukatsu, A., Hayashi, T., et al. (2007) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.107.142182 · Cited by 102
Self-citationA review of endothelial dysfunction in diabetes: a focus on the contribution of a dysfunctional eNOS
Triggle, C. R., & Ding, H. (2010) · Journal of the American Society of Hypertension · doi:10.1016/j.jash.2010.02.004 · Cited by 103
Endothelial dysfunction in diabetes: multiple targets for treatment
Ding, H., & Triggle, C. R. (2010) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-010-0807-3 · Cited by 101
Whitsett, J., Picklo, M. J., & Vasquez-Vivar, J. M. (2007) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.107.153742 · Cited by 92
Wohlfart, P., Xu, H., Endlich, A., Habermeier, A., Closs, E. I., Hübschle, T., Mang, C. F., Strobel, H., Suzuki, T. C., Kleinert, H., et al. (2008) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.107.128009 · Cited by 91
Wood, K. C., Hebbel, R. P., Lefer, D. J., & Granger, D. N. (2006) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2005.12.015 · Cited by 87
Rakovich, T. Y., Boland, C., Bernstein, I. R., Chikwana, V. M., Iwata‐Reuyl, D., & Kelly, V. P. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.219576 · Cited by 85
Tetrahydrobiopterin, superoxide, and vascular dysfunction
Vásquez-Vivar, J. (2009) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2009.07.024 · Cited by 84
Therapeutic Potential of Tetrahydrobiopterin for Treating Vascular and Cardiac Disease
Moens, A. L., & Kass, D. A. (2007) · Journal of Cardiovascular Pharmacology · doi:10.1097/fjc.0b013e318123f854 · Cited by 83
Shishido, T., Nozaki, N., Takahashi, H., Arimoto, T., Niizeki, T., Koyama, Y., Abe, J., Takeishi, Y., & Kubota, I. (2006) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2006.05.056 · Cited by 83
GCH1 Haplotype Determines Vascular and Plasma Biopterin Availability in Coronary Artery Disease
Antoniades, C. A., Shirodaria, C. C., Assche, T. V., Cunnington, C., Tegeder, I., Lötsch, J., Guzik, T. J., Leeson, P., Diesch, J., Tousoulis, D., et al. (2008) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2007.12.062 · Cited by 79
Self-citationCardiac nitric oxide: Emerging role for nNOS in regulating physiological function
Danson, E., Choate, J., & Paterson, D. J. (2005) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2004.11.003 · Cited by 77
Wang, J., Wang, Y., Huang, J.-Y., Yang, Z., Chen, L., Wang, L.-C., Tang, A.-L., Lou, Z.-F., & Tao, J. (2007) · Journal of Vascular Research · doi:10.1159/000100558 · Cited by 73
Ferroptosis and Its Potential Role in Metabolic Diseases: A Curse or Revitalization?
Duan, J.-Y., Lin, X., Xu, F., Shan, S., Guo, B., Li, F., Wang, Y., Zheng, M.-H., Xu, Q.-S., Lei, L.-M., et al. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.701788 · Cited by 69
Hattori, Y., Hattori, S., Wang, X., Satoh, H., Nakanishi, N., & Kasai, K. (2007) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/01.atv.0000258946.55438.0e · Cited by 66
Chuaiphichai, S., McNeill, E., Douglas, G., Crabtree, M. J., Bendall, J. K., Hale, A. B., Alp, N. J., & Channon, K. M. (2014) · Hypertension · doi:10.1161/hypertensionaha.114.03089 · Cited by 63
Self-citationChen, K., Zhou, X., Jiang, W., Wu, P., Liu, Y., Jiang, J., Kuang, S., Tang, L., Tang, W., Zhang, Y., et al. (2018) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2017.12.060 · Cited by 61
The role of tetrahydrobiopterin in inflammation and cardiovascular disease
McNeill, E., & Channon, K. M. (2012) · Thrombosis and Haemostasis · doi:10.1160/th12-06-0424 · Cited by 61
Self-citationMusicki, B., Liu, T., Strong, T., Jin, L., Laughlin, M. H., Turk, J. R., & Burnett, A. L. (2008) · The Journal of Sexual Medicine · doi:10.1111/j.1743-6109.2007.00731.x · Cited by 58
Daiber, A., Steven, S., Vujačić-Mirski, K., Kalinovic, S., Oelze, M. W., Lisa, F. D., & Münzel, T. F. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21103405 · Cited by 59
Plasma Tetrahydrobiopterin/Dihydrobiopterin Ratio A Possible Marker of Endothelial Dysfunction
Takeda, M., Yamashita, T., Shinohara, M., Sasaki, N., Takaya, T., Nakajima, K., Inoue, N., Masano, T., Tawa, H., Satomi‐Kobayashi, S., et al. (2009) · Circulation Journal · doi:10.1253/circj.cj-08-0850 · Cited by 58
Functional alterations in endothelial NO, PGI2 and EDHF pathways in aorta in ApoE/LDLR−/− mice
Csányi, G., Gajda, M., Franczyk‐Żarów, M., Kostogrys, R. B., Gwóźdź, P., Mateuszuk, Ł., Sternak, M., Wójcik, L., Zalewska, T., Walski, M., et al. (2012) · Prostaglandins & Other Lipid Mediators · doi:10.1016/j.prostaglandins.2012.02.002 · Cited by 54
Ceylan‐Isik, A. F., Guo, K. K., Carlson, E. C., Privratsky, J. R., Liao, S.-J., Cai, L. F., Chen, A. F., & Ren, J. T. (2009) · Hypertension · doi:10.1161/hypertensionaha.108.123422 · Cited by 55
Sasaki, N., Yamashita, T., Takaya, T., Shinohara, M., Shiraki, R., Takeda, M., Emoto, N., Fukatsu, A., Hayashi, T., Ikemoto, K., et al. (2008) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.107.160754 · Cited by 56
A novel role for endothelial tetrahydrobiopterin in mitochondrial redox balance
Bailey, J. D., Shaw, A., Fischer, R., Ryan, B. J., Kessler, B. M., McCullagh, J., Wade‐Martins, R., Channon, K. M., & Crabtree, M. J. (2017) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2017.01.012 · Cited by 53
Self-citationNitric oxide, angiotensin II, and reactive oxygen species in hypertension and atherogenesis
Schulman, I. H., Zhou, M.-S., & Raij, L. R. (2005) · Current Hypertension Reports · doi:10.1007/s11906-005-0056-6 · Cited by 56
Suppression of eNOS-derived superoxide by caveolin-1: a biopterin-dependent mechanism
Karuppiah, K. M., Druhan, L. J., Chen, C., Smith, T., Zweier, J. L., Sessa, W. C., & Cardounel, A. J. (2011) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00936.2010 · Cited by 49
Antioxidants and endothelial nitric oxide synthesis
Heller, R., Werner‐Felmayer, G., & Werner, E. R. (2005) · European Journal of Clinical Pharmacology · doi:10.1007/s00228-005-0009-7 · Cited by 48
Leiva, A., Fuenzalida, B., Barros, E., Sobrevia, B., Salsoso, R., Sáez, T., Villalobos-Labra, R., Silva, L., Chiarello, D. I., Toledo, F., et al. (2016) · Current Vascular Pharmacology · doi:10.2174/1570161114666160222115158 · Cited by 50
Tetrahydrobiopterin in energy metabolism and metabolic diseases
Kim, H. K., & Han, J. (2020) · Pharmacological Research · doi:10.1016/j.phrs.2020.104827 · Cited by 50
Oidor-Chan, V. H., Hong, E., Pérez‐Severiano, F., Montes, S., Torres-Narváez, J. C., del Valle‐Mondragón, L., Pastelín-Hernández, G. S., & Sánchez-Mendoza, A. (2016) · PPAR Research · doi:10.1155/2016/8237264 · Cited by 46
Effects of resveratrol on eNOS in the endothelium and the perivascular adipose tissue
Xia, N., Förstermann, U., & Li, H. (2017) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.13397 · Cited by 44
Modeling of biopterin-dependent pathways of eNOS for nitric oxide and superoxide production
Kar, S., & Kavdia, M. (2011) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2011.06.009 · Cited by 42
Regulation of Endothelial Cell Tetrahydrobiopterin
Harrison, D. G., Chen, W., Dikalov, S., & Li, L. (2010) · Advances in pharmacology · doi:10.1016/b978-0-12-385061-4.00005-2 · Cited by 41
Metadata
- Authors
- Alp, N. J., McAteer, M. A., Khoo, J., Choudhury, R. P., & Channon, K. M.
- Affiliations
- John Radcliffe Hospital (GB)
- Venue
- Arteriosclerosis, Thrombosis, and Vascular Biology
- Published
- 2004-03
- Volume
- 24
- Issue
- 3
- Pages
- 445-450
- ISSN
- 1079-5642 (ISSN-L)
- 1524-4636
- OpenAlex
- W2172004618
- Cited by
- 194
- References
- 34
- Citations by year
- 2025: 5 · 2024: 1 · 2023: 4 · 2022: 4 · 2021: 2 · 2020: 7 · 2019: 6 · 2018: 7 · 2017: 11 · 2016: 7 · 2015: 4 · 2014: 17 · 2013: 10 · 2012: 13
- FWCI
- 8.55
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Arteriosclerosis Thrombosis and Vascular Biology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Wellcome Trust
- British Heart Foundation
- Topics
- Health Sciences › Medicine › Physiology (medical) › Nitric Oxide and Endothelin Effects
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiovascular Health and Disease Prevention
- Life Sciences › Immunology and Microbiology › Immunology › Atherosclerosis and Cardiovascular Diseases
- Keywords
- tetrahydrobiopterin, GTP cyclohydrolase I, endothelial dysfunction, atherosclerosis, endothelial nitric oxide synthase, nitric oxide bioactivity, eNOS uncoupling, superoxide production, cGMP signaling, ApoE-deficient mice, high-fat diet, aortic plaque, transgenic mice
- MeSH terms
- Animals, Aorta, Aortic Diseases, Apolipoproteins E, Arteriosclerosis, Biopterins, Coenzymes, Crosses, Genetic, Diet, Atherogenic, Endothelium, Vascular, GTP Cyclohydrolase, Cyclic GMP, Humans, Hyperlipoproteinemia Type II, Hyperlipoproteinemia Type IV, Mice, Inbred C57BL, Mice, Transgenic, Nitric Oxide, Organ Specificity, Recombinant Fusion Proteins, Superoxides, Vasodilation, Mice, Knockout, Receptor, TIE-2, Mice
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