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Journal articles on the topic 'Haeme-oxygenase'

Author: Grafiati
Published: 2 June 2025
Last updated: 31 July 2025

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1

Ndisang, Joseph Fomusi, Rui Wang, Alfredo Vannacci, et al. "Haeme oxygenase-1 and cardiac anaphylaxis." British Journal of Pharmacology 134, no. 8 (2001): 1689–96. http://dx.doi.org/10.1038/sj.bjp.0704427.

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2

Fredenburgh, Laura E., Allison A. Merz, and Susan Cheng. "Haeme oxygenase signalling pathway: implications for cardiovascular disease." European Heart Journal 36, no. 24 (2015): 1512–18. http://dx.doi.org/10.1093/eurheartj/ehv114.

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3

Calò, Lorenzo A., Paul A. Davis, Andrea Semplicini, and Achille C. Pessina. "l-Carnitine and erythropoiesis: relationship with haeme oxygenase-1." Nephrology Dialysis Transplantation 20, no. 8 (2005): 1769–70. http://dx.doi.org/10.1093/ndt/gfh934.

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4

Sacca, P., R. Meiss, G. Casas, et al. "Nuclear translocation of haeme oxygenase-1 is associated to prostate cancer." British Journal of Cancer 97, no. 12 (2007): 1683–89. http://dx.doi.org/10.1038/sj.bjc.6604081.

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5

Smith, Abigail F., and George Loo. "Upregulation of haeme oxygenase-1 by zinc in HCT-116 cells." Free Radical Research 46, no. 9 (2012): 1099–107. http://dx.doi.org/10.3109/10715762.2012.690872.

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6

Syapin, P. J. "Regulation of haeme oxygenase-1 for treatment of neuroinflammation and brain disorders." British Journal of Pharmacology 155, no. 5 (2008): 623–40. http://dx.doi.org/10.1038/bjp.2008.342.

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7

Steiner, A. A., L. G. S. Branco, F. Q. Cunha, and S. H. Ferreira. "Role of the haeme oxygenase/carbon monoxide pathway in mechanical nociceptor hypersensitivity." British Journal of Pharmacology 132, no. 8 (2001): 1673–82. http://dx.doi.org/10.1038/sj.bjp.0704014.

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8

Vargas, Hilda, Carlos Castillo, Francisco Posadas, and Bruno Escalante. "Acute lead exposure induces renal haeme oxygenase-1 and decreases urinary Na excretion." Human & Experimental Toxicology 22, no. 5 (2003): 237–44. http://dx.doi.org/10.1191/0960327103ht360oa.

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The effects of acute lead exposure on renal function, lipid peroxidation and the expression of haeme oxygenase (HO) in rat kidney were determined. A single injection of lead acetate (50 mg Pb/kg) was given to rats. Changes in renal function, characterized by a significant reduction in the Na excretion was observed six hours after Pb exposure; this effect persisted for 24 hours. TBARS levels increased in kidney cortex 24 hours after Pb administration. In kidney cortex, Pb exposure affected the expression of HO-1, a renal protein associated with oxidative stress. HO-1 mRNA increased 2.3-fold, th
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9

Taye, Ashraf, and Badr Mostafa Ibrahim. "Activation of renal haeme oxygenase-1 alleviates gentamicin-induced acute nephrotoxicity in rats." Journal of Pharmacy and Pharmacology 65, no. 7 (2013): 995–1004. http://dx.doi.org/10.1111/jphp.12067.

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10

Wojas-Pelc, Anna, and Janusz Marcinkiewicz. "What is a role of haeme oxygenase-1 in psoriasis? Current concepts of pathogenesis." International Journal of Experimental Pathology 88, no. 2 (2006): 95–102. http://dx.doi.org/10.1111/j.1365-2613.2006.00505.x.

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11

Vashist, Yogesh K., Guentac Uzunoglu, Guelle Cataldegirmen, et al. "Haeme oxygenase-1 promoter polymorphism is an independent prognostic marker of gastrointestinal stromal tumour." Histopathology 54, no. 3 (2009): 303–8. http://dx.doi.org/10.1111/j.1365-2559.2009.03221.x.

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12

Bolognesi, M. "Haeme oxygenase mediates hyporeactivity to phenylephrine in the mesenteric vessels of cirrhotic rats with ascites." Gut 54, no. 11 (2005): 1630–36. http://dx.doi.org/10.1136/gut.2004.063735.

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13

Ono, Koh, Toshifumi Mannami, and Naoharu Iwai. "Association of a promoter variant of the haeme oxygenase-1 gene with hypertension in women." Journal of Hypertension 21, no. 8 (2003): 1497–503. http://dx.doi.org/10.1097/00004872-200308000-00013.

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14

Gutierrez, Fredy R. S., Wander R. Pavanelli, Tiago S. Medina, et al. "Haeme oxygenase activity protects the host against excessive cardiac inflammation during experimental Trypanosoma cruzi infection." Microbes and Infection 16, no. 1 (2014): 28–39. http://dx.doi.org/10.1016/j.micinf.2013.10.007.

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15

Liu, Da-Nan, Ying Fang, Li-Rong Wu, Xing-De Liu, Ping Li, and Zuo-Yun He. "Effect of the haeme oxygenase-1/endogenous carbon monoxide system on atherosclerotic plaque formation in rabbits." CardioVascular Journal of Africa 21, no. 5 (2010): 257–62. http://dx.doi.org/10.5830/cvja-2010-015.

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16

Der Sarkissian, S., J.-F. Cailhier, M. Borie, et al. "Celastrol protects ischaemic myocardium through a heat shock response with up-regulation of haeme oxygenase-1." British Journal of Pharmacology 171, no. 23 (2014): 5265–79. http://dx.doi.org/10.1111/bph.12838.

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17

Tongers, J., J. M. Knapp, M. Korf, et al. "Haeme oxygenase promotes progenitor cell mobilization, neovascularization, and functional recovery after critical hindlimb ischaemia in mice." Cardiovascular Research 78, no. 2 (2008): 294–300. http://dx.doi.org/10.1093/cvr/cvm107.

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18

Gorman, Des, Y. L. Huang, and Chris Williams. "A narcotic dose of carbon monoxide induces neuronal haeme oxygenase and nitric oxide synthetase in sheep." Toxicology 179, no. 1-2 (2002): 79–84. http://dx.doi.org/10.1016/s0300-483x(02)00339-6.

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19

Xia, Zhong-yuan, Jin Gao, Ameer Kumar Ancharaz, Ke-xuan Liu, Zhengyuan Xia, and Tao Luo. "Ischaemic post-conditioning protects lung from ischaemia–reperfusion injury by up-regulation of haeme oxygenase-1." Injury 41, no. 5 (2010): 510–16. http://dx.doi.org/10.1016/j.injury.2009.03.002.

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20

Gorman, Des, and Yi Lin Huang. "Haeme oxygenase and nitric oxide synthetase blockade and brain blood flow in sheep exposed to carbon monoxide." Neuroscience Letters 444, no. 2 (2008): 203–7. http://dx.doi.org/10.1016/j.neulet.2008.08.038.

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21

Xu, J. J., and Y. L. Wang. "Propofol attenuation of hydrogen peroxide-mediated oxidative stress and apoptosis in cultured cardiomyocytes involves haeme oxygenase-1." European Journal of Anaesthesiology 25, no. 5 (2008): 395–402. http://dx.doi.org/10.1017/s0265021508003542.

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22

Berglund, L., B. Angelin, R. Hultcrantz, et al. "Studies with the haeme oxygenase inhibitor Sn-protoporphyrin in patients with primary biliary cirrhosis and idiopathic haemochromatosis." Gut 31, no. 8 (1990): 899–904. http://dx.doi.org/10.1136/gut.31.8.899.

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23

Nam, S. Y., and K. Sabapathy. "p53 promotes cellular survival in a context-dependent manner by directly inducing the expression of haeme-oxygenase-1." Oncogene 30, no. 44 (2011): 4476–86. http://dx.doi.org/10.1038/onc.2011.150.

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24

Egea, Javier, Angelo O. Rosa, Silvia Lorrio, Laura del Barrio, Antonio Cuadrado, and Manuela G. López. "Haeme oxygenase-1 overexpression via nAChRs and the transcription factor Nrf2 has antinociceptive effects in the formalin test." Pain 146, no. 1 (2009): 75–83. http://dx.doi.org/10.1016/j.pain.2009.07.007.

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25

Park, Na-Young, Seul-Ki Park, and Yunsook Lim. "Long-term dietary antioxidant cocktail supplementation effectively reduces renal inflammation in diabetic mice." British Journal of Nutrition 106, no. 10 (2011): 1514–21. http://dx.doi.org/10.1017/s0007114511001929.

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Diabetic nephropathy is a serious complication for diabetic patients, yet the precise mechanism that underlies the development of diabetic complications remains unknown. We hypothesised that dietary antioxidant supplementation with single N-acetylcysteine (NAC) or vitamin C combined with either vitamin E or vitamin E and NAC improves diabetic renal inflammation through the modulation of blood glucose levels, oxidative stress and inflammatory response. Experimental animals were treated with alloxan monohydrate to induce diabetes. Mice were divided into five groups and supplemented with single o
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26

Elies, J., C. Peers C, and F. Del Galdo. "A9.03 Exploring the potential of haeme-oxygenase 1 (HO-1) as a therapeutic target for pah associated with CTD." Annals of the Rheumatic Diseases 75, Suppl 1 (2016): A71.1—A71. http://dx.doi.org/10.1136/annrheumdis-2016-209124.169.

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27

Jonas, J. C., Y. Guiot, J. Rahier, and J. C. Henquin. "Haeme-oxygenase 1 expression in rat pancreatic beta cells is stimulated by supraphysiological glucose concentrations and by cyclic AMP." Diabetologia 46, no. 9 (2003): 1234–44. http://dx.doi.org/10.1007/s00125-003-1174-9.

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28

Henquin, J. C., J. C. Jonas, Y. Guiot, and J. Rahier. "Haeme-oxygenase 1 expression in rat pancreatic beta cells is stimulated by supraphysiological glucose concentrations and by cyclic AMP." Diabetologia 47, no. 4 (2004): 765. http://dx.doi.org/10.1007/s00125-004-1376-9.

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29

Haines, D. D., I. Lekli, P. Teissier, I. Bak, and A. Tosaki. "Role of haeme oxygenase-1 in resolution of oxidative stress-related pathologies: focus on cardiovascular, lung, neurological and kidney disorders." Acta Physiologica 204, no. 4 (2012): 487–501. http://dx.doi.org/10.1111/j.1748-1716.2011.02387.x.

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30

Rahman, Z., DK Dwivedi, and GB Jena. "Ethanol-induced gastric ulcer in rats and intervention of tert-butylhydroquinone: Involvement of Nrf2/HO-1 signalling pathway." Human & Experimental Toxicology 39, no. 4 (2019): 547–62. http://dx.doi.org/10.1177/0960327119895559.

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Gastric ulcer (GU) is the most common health concern that occurs due to alcohol consumption, smoking and physiological stress. Ethanol-induced GU in animal model resembles the pathophysiology of human ulcer. The present study was designed to investigate the cytoprotective and anti-inflammatory properties of tert-butylhydroquinone (tBHQ), a nuclear factor erythroid 2-related factor 2 (Nrf2) activator, against gastric mucosal damage induced by acute exposure of ethanol (5 ml/kg). The intervention of tBHQ (25 and 50 mg/kg, per os (po)) and omeprazole (20 mg/kg, po) was done for 10 consecutive day
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31

Sammut, Ivan A., Roberta Foresti, James E. Clark, et al. "Carbon monoxide is a major contributor to the regulation of vascular tone in aortas expressing high levels of haeme oxygenase-1." British Journal of Pharmacology 125, no. 7 (1998): 1437–44. http://dx.doi.org/10.1038/sj.bjp.0702212.

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32

Herden, C., H. J. Schluesener, and J. A. Richt. "Expression of allograft inflammatory factor-1 and haeme oxygenase-1 in brains of rats infected with the neurotropic Borna disease virus." Neuropathology and Applied Neurobiology 31, no. 5 (2005): 512–21. http://dx.doi.org/10.1111/j.1365-2990.2005.00668.x.

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33

Elouil, H., A. K. Cardozo, D. L. Eizirik, J. C. Henquin та J. C. Jonas. "High glucose and hydrogen peroxide increase c-Myc and haeme-oxygenase 1 mRNA levels in rat pancreatic islets without activating NFκB". Diabetologia 48, № 12 (2005): 2693. http://dx.doi.org/10.1007/s00125-005-0043-0.

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34

Elouil, H., A. K. Cardozo, D. L. Eizirik, J. C. Henquin, and J. C. Jonas. "High glucose and hydrogen peroxide increase c-Myc and haeme-oxygenase 1 mRNA levels in rat pancreatic islets without activating NF?B." Diabetologia 48, no. 3 (2005): 496–505. http://dx.doi.org/10.1007/s00125-004-1664-4.

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35

Pagano, Giovanni, Annarita Aiello Talamanca, Giuseppe Castello, Federico V. Pallardó, Adriana Zatterale, and Paolo Degan. "Oxidative stress in Fanconi anaemia: from cells and molecules towards prospects in clinical management." Biological Chemistry 393, no. 1-2 (2012): 11–21. http://dx.doi.org/10.1515/bc-2011-227.

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Abstract Fanconi anaemia (FA) is a genetic disease featuring bone marrow failure, proneness to malignancies, and chromosomal instability. A line of studies has related FA to oxidative stress (OS). This review attempts to evaluate the evidence for FA-associated redox abnormalities in the literature from 1981 to 2010. Among 2170 journal articles on FA evaluated, 162 related FA with OS. Early studies reported excess oxygen toxicity in FA cells that accumulated oxidative DNA damage. Prooxidant states were found in white blood cells and body fluids from FA patients as excess luminol-dependent chemi
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36

Đurašević, Stojković, Bogdanović, et al. "The Effects of Meldonium on the Renal Acute Ischemia/Reperfusion Injury in Rats." International Journal of Molecular Sciences 20, no. 22 (2019): 5747. http://dx.doi.org/10.3390/ijms20225747.

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Acute renal ischemia/reperfusion (I/R) injury is a clinical condition that is challenging to treat. Meldonium is an anti-ischemic agent that shifts energy production from fatty acid oxidation to less oxygen-consuming glycolysis. Thus, in this study we investigated the effects of a four-week meldonium pre-treatment (300 mg/kg b.m./day) on acute renal I/R in male rats (Wistar strain). Our results showed that meldonium decreased animal body mass gain, food and water intake, and carnitine, glucose, and lactic acid kidney content. In kidneys of animals subjected to I/R, meldonium increased phosphor
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37

Lee, Jin-Ching, Chin-Kai Tseng, Kung-Chia Young, et al. "Andrographolide exerts anti-hepatitis C virus activity by up-regulating haeme oxygenase-1 via the p38 MAPK/Nrf2 pathway in human hepatoma cells." British Journal of Pharmacology 171, no. 1 (2013): 237–52. http://dx.doi.org/10.1111/bph.12440.

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38

Park, H. J., B. T. Jeon, H. C. Kim, et al. "Aged red garlic extract reduces lipopolysaccharide-induced nitric oxide production in RAW 264.7 macrophages and acute pulmonary inflammation through haeme oxygenase-1 induction." Acta Physiologica 205, no. 1 (2012): 61–70. http://dx.doi.org/10.1111/j.1748-1716.2012.02425.x.

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39

Rosa, Angelo O., Javier Egea, Silvia Lorrio, Ana I. Rojo, Antonio Cuadrado, and Manuela G. López. "Nrf2-mediated haeme oxygenase-1 up-regulation induced by cobalt protoporphyrin has antinociceptive effects against inflammatory pain in the formalin test in mice." Pain 137, no. 2 (2008): 332–39. http://dx.doi.org/10.1016/j.pain.2007.09.015.

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40

Mueller, Kristin, Nicole M. Blum, Holger Kluge, and Andreas S. Mueller. "Influence of broccoli extract and various essential oils on performance and expression of xenobiotic- and antioxidant enzymes in broiler chickens." British Journal of Nutrition 108, no. 4 (2011): 588–602. http://dx.doi.org/10.1017/s0007114511005873.

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The aim of our present study was to examine the regulation of xenobiotic- and antioxidant enzymes by phytogenic feed additives in the intestine and the liver of broilers. A total of 240 male Ross-308 broiler chickens (1 d old) were fed a commercial starter diet for 2 weeks. On day 15, the birds were assigned to six treatment groups of forty birds each. The control (Con) group was fed a diet without any additive for 3 weeks. The diet of group sulforaphane (SFN) contained broccoli extract providing 0·075 g/kg SFN, whereas the diets of the other four groups contained 0·15 g/kg essential oils from
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41

Polla, BS, S. Kantengwa, GJ Gleich, M. Kondo, CM Reimert, and AF Junod. "Spontaneous heat shock protein synthesis by alveolar macrophages in interstitial lung disease associated with phagocytosis of eosinophils." European Respiratory Journal 6, no. 4 (1993): 483–88. http://dx.doi.org/10.1183/09031936.93.06040483.

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Synthesis of heat shock proteins (HSPs) is induced in all cells and tissues after exposure to elevated temperatures, or a variety of other types of injury, including oxidative injury. We have previously reported that stress proteins are induced in monocytes-macrophages during phagocytosis of red blood cells. Receptor-mediated phagocytosis is associated with activation of the respiratory burst, generation of the lipid mediators of inflammation, and increased production of cytokines. Similar activation events have been described in the alveolar macrophage (AM) during pulmonary fibrosis. We there
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42

Jancsó, Zsanett, and Edit Hermesz. "Impact of acute arsenic and cadmium exposure on the expression of two haeme oxygenase genes and other antioxidant markers in common carp (Cyprinus carpio)." Journal of Applied Toxicology 35, no. 3 (2014): 310–18. http://dx.doi.org/10.1002/jat.3000.

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43

Meiller, A., S. Alvarez, P. Drane, et al. "p53-dependent stimulation of redox-related genes in the lymphoid organs of -irradiated mice identification of Haeme-oxygenase 1 as a direct p53 target gene." Nucleic Acids Research 35, no. 20 (2007): 6924–34. http://dx.doi.org/10.1093/nar/gkm824.

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44

Sahin, Kazim, Cemal Orhan, Mehmet Tuzcu, et al. "Berberis vulgaris root extract alleviates the adverse effects of heat stress via modulating hepatic nuclear transcription factors in quails." British Journal of Nutrition 110, no. 4 (2013): 609–16. http://dx.doi.org/10.1017/s0007114512005648.

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To evaluate the action mode of Berberis vulgaris root extract in the alleviation of oxidative stress, female Japanese quails (n 180, aged 5 weeks) were reared, either at 22°C for 24 h/d (thermoneutral, TN) or 34°C for 8 h/d (heat stress, HS), and fed one of three diets: diets containing 0, 100 or 200 mg of B. vulgaris root extract per kg for 12 weeks. Exposure to HS depressed feed intake by 8·5 % and egg production by 12·1 %, increased hepatic malondialdehyde (MDA) level by 98·0 % and decreased hepatic superoxide dismutase, catalase and glutathione peroxidase activities by 23·5, 35·4 and 55·7
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45

Choi, Eun-Young, Ji-Young Jin, Jeom-Il Choi, In Soon Choi, and Sung-Jo Kim. "DHA suppressesPrevotella intermedialipopolysaccharide-induced production of proinflammatory mediators in murine macrophages." British Journal of Nutrition 111, no. 7 (2013): 1221–30. http://dx.doi.org/10.1017/s0007114513003681.

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Several reports have indicated that dietary intake of DHA is associated with lower prevalence of periodontitis. In the present study, we investigated the effect of DHA on the production of proinflammatory mediators in murine macrophage-like RAW264.7 cells stimulated with lipopolysaccharide (LPS) isolated fromPrevotellaintermedia, a pathogen implicated in inflammatory periodontal disease, and its mechanisms of action. LPS was isolated from lyophilisedP.intermediaATCC 25 611 cells using the standard hot-phenol–water protocol. Culture supernatants were collected and assayed for NO, IL-1β and IL-6
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46

Zheng, Adi, Hao Li, Jie Xu, et al. "Hydroxytyrosol improves mitochondrial function and reduces oxidative stress in the brain of db/db mice: role of AMP-activated protein kinase activation." British Journal of Nutrition 113, no. 11 (2015): 1667–76. http://dx.doi.org/10.1017/s0007114515000884.

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Hydroxytyrosol (HT) is a major polyphenolic compound found in olive oil with reported anti-cancer and anti-inflammatory activities. However, the neuroprotective effect of HT on type 2 diabetes remains unknown. In the present study, db/db mice and SH-SY-5Y neuroblastoma cells were used to evaluate the neuroprotective effects of HT. After 8 weeks of HT administration at doses of 10 and 50 mg/kg, expression levels of the mitochondrial respiratory chain complexes I/II/IV and the activity of complex I were significantly elevated in the brain of db/db mice. Likewise, targets of the antioxidative tra
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47

Wang, X., L. Li, and G. Zhang. "Quercetin protects the buffalo rat liver (BRL-3A) cells from aflatoxin B1-induced cytotoxicity via activation of Nrf2-ARE pathway." World Mycotoxin Journal 13, no. 2 (2020): 299–312. http://dx.doi.org/10.3920/wmj2019.2465.

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Aflatoxin B1 (AFB1) is the most toxic mycotoxin widely presented in agricultural products, and the protective effect of quercetin (QUE), a natural antioxidant, against AFB1-induced cytotoxicity to the buffalo rat liver (BRL-3A) cells was investigated. With an IC50 of 23 μM, AFB1 induced a significant oxidative stress to BRL-3A cells evidenced by a dose-dependent reduction of mitochondria membrane potential (MMP), ATP content, and activities of endogenous antioxidant enzymes along with increased levels of reactive oxygen species (ROS) and lipid peroxidation biomarker of malondialdehyde (MDA). T
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48

Giacomo, Claudia Di, Rosaria Acquaviva, Andrea Piva та ін. "Protective effect of cyanidin 3-O-β-d-glucoside on ochratoxin A-mediated damage in the rat". British Journal of Nutrition 98, № 5 (2007): 937–43. http://dx.doi.org/10.1017/s0007114507756908.

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The aim of the present study was to verify whether the oral administration of cyanidin 3-O-β-d-glucoside (C3G) might counteract damage induced by chronic exposure (28 d) to ochratoxin A (OTA) in rats and if its effect may be mediated by haeme oxygenase-1 (HO-1). Forty male Sprague–Dawley rats, individually caged, were divided into four groups of ten animals. A control group received a commercial diet, group C3G received the control diet supplemented with C3G (1 g/kg feed), group OTA received the control diet supplemented with 200 parts per billion of OTA, and group OTA+C3G received the OTA gro
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49

Ide, Takashi. "Effect of dietary α-lipoic acid on the mRNA expression of genes involved in drug metabolism and antioxidation system in rat liver". British Journal of Nutrition 112, № 3 (2014): 295–308. http://dx.doi.org/10.1017/s0007114514000841.

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In the present study, the mRNA levels of hepatic proteins involved in the drug metabolism of rats fed α-lipoic acid were evaluated by DNA microarray and real-time PCR analyses. Experimental diets containing 0, 0·1, 0·25 and 0·5 % (w/w) α-lipoic acid were fed to four groups of rats consisting of seven animals each for 21 d. DNA microarray analysis revealed that the diet containing 0·5 % α-lipoic acid significantly (P< 0·05) increased the mRNA levels of various phase I drug-metabolising enzymes up to 15-fold and phase II enzymes up to 52-fold in an isoenzyme-specific manner. α-Lipoic acid als
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50

Damulewicz, Milena, Agnieszka Loboda, Alicja Jozkowicz, Jozef Dulak, and Elzbieta Pyza. "Haeme oxygenase protects against UV light DNA damages in the retina in clock-dependent manner." Scientific Reports 7, no. 1 (2017). http://dx.doi.org/10.1038/s41598-017-05418-6.

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