hydrogen sulfide has been researched along with Obesity in 35 studies
Hydrogen Sulfide: A flammable, poisonous gas with a characteristic odor of rotten eggs. It is used in the manufacture of chemicals, in metallurgy, and as an analytical reagent. (From Merck Index, 11th ed)
hydrogen sulfide : A sulfur hydride consisting of a single sulfur atom bonded to two hydrogen atoms. A highly poisonous, flammable gas with a characteristic odour of rotten eggs, it is often produced by bacterial decomposition of organic matter in the absence of oxygen.
thiol : An organosulfur compound in which a thiol group, -SH, is attached to a carbon atom of any aliphatic or aromatic moiety.
Obesity: A status with BODY WEIGHT that is grossly above the recommended standards, usually due to accumulation of excess FATS in the body. The standards may vary with age, sex, genetic or cultural background. In the BODY MASS INDEX, a BMI greater than 30.0 kg/m2 is considered obese, and a BMI greater than 40.0 kg/m2 is considered morbidly obese (MORBID OBESITY).
| Excerpt | Relevance | Reference |
|---|---|---|
| "Hydrogen sulfide (H(2)S) is a vasodilatory gasotransmitter mediator in the cardiovascular system, proposed as an endothelium-derived relaxing factor." | 6.47 | Hydrogen sulfide and the metabolic syndrome. ( Chang, T; Desai, KM; Untereiner, A; Wu, L, 2011) |
| "Hydrogen sulfide (H2S) is an essential neuromodulator, generates by cystathionine β synthase (CBS) or 3-mecaptopyruvate sulfurtransferase (3MST) in the brain." | 5.48 | Cystathionine beta synthase-hydrogen sulfide system in paraventricular nucleus reduced high fatty diet induced obesity and insulin resistance by brain-adipose axis. ( Cai, J; Cui, C; Cui, Q; Geng, B; Han, J; Lu, H; Tang, C; Xu, G; Yang, J; Zheng, F; Zhou, Y, 2018) |
| "Obesity was found to be associated with decreased vessel H2S concentration, inward hypertrophic remodeling, altered collagen-to-elastin ratio, and reduced vessel stiffness." | 5.43 | Hydrogen sulfide depletion contributes to microvascular remodeling in obesity. ( Candela, J; Velmurugan, GV; White, C, 2016) |
| "Hydrogen-rich water has a significant protective effect on OGD/R-causing HT22 cell injury, and the mechanism may be related to the inhibition of autophagy." | 4.40 | Effect of 12-week of aerobic exercise on hormones and lipid profile status in adolescent girls with polycystic ovary syndrome: A study during COVID-19. ( , 2023) |
| "Dietary methionine restriction (MR) has been reported to extend lifespan, reduce obesity and decrease oxidative damage to mtDNA in the heart of rats, and increase endogenous hydrogen sulfide (H2S) production in the liver and blood." | 3.96 | Dietary methionine restriction improves the impairment of cardiac function in middle-aged obese mice. ( Feng, C; Ge, Y; Han, L; Jiang, Y; Le, G; Li, B; Shi, Y; Wu, G; Yang, Y, 2020) |
| "Obesity is associated with elevated plasma cysteine, whereas diabetes is associated with reduced cysteine levels." | 2.53 | Cysteine and hydrogen sulphide in the regulation of metabolism: insights from genetics and pharmacology. ( Carter, RN; Morton, NM, 2016) |
| "Hyperglycemia has been consistently demonstrated to suppress CSE-H₂S pathway in various adipose tissue depots." | 2.53 | Hydrogen Sulfide in the Adipose Tissue-Physiology, Pathology and a Target for Pharmacotherapy. ( Bełtowski, J; Jamroz-Wiśniewska, A, 2016) |
| "Hydrogen sulfide (H(2)S) is a vasodilatory gasotransmitter mediator in the cardiovascular system, proposed as an endothelium-derived relaxing factor." | 2.47 | Hydrogen sulfide and the metabolic syndrome. ( Chang, T; Desai, KM; Untereiner, A; Wu, L, 2011) |
| " Chronic administration of NaSH in particular at high doses impaired carbohydrate metabolism in type 2 diabetic rats." | 1.51 | Effects of Hydrogen Sulfide on Carbohydrate Metabolism in Obese Type 2 Diabetic Rats. ( Ghasemi, A; Gheibi, S; Jeddi, S; Kashfi, K, 2019) |
| "Hydrogen sulfide (H2S) is an essential neuromodulator, generates by cystathionine β synthase (CBS) or 3-mecaptopyruvate sulfurtransferase (3MST) in the brain." | 1.48 | Cystathionine beta synthase-hydrogen sulfide system in paraventricular nucleus reduced high fatty diet induced obesity and insulin resistance by brain-adipose axis. ( Cai, J; Cui, C; Cui, Q; Geng, B; Han, J; Lu, H; Tang, C; Xu, G; Yang, J; Zheng, F; Zhou, Y, 2018) |
| "Obesity was found to be associated with decreased vessel H2S concentration, inward hypertrophic remodeling, altered collagen-to-elastin ratio, and reduced vessel stiffness." | 1.43 | Hydrogen sulfide depletion contributes to microvascular remodeling in obesity. ( Candela, J; Velmurugan, GV; White, C, 2016) |
| " Endothelial function and NO bioavailability were significantly reduced in the WD group (p < 0." | 1.43 | Decreased vascular H2S production is associated with vascular oxidative stress in rats fed a high-fat western diet. ( Hart, JL; Jenkins, TA; Nguyen, JC, 2016) |
| "Hydrogen sulfide (H2S) plays an important role in renal physiological and pathophysiological processes." | 1.43 | Hydrogen Sulfide Mitigates Kidney Injury in High Fat Diet-Induced Obese Mice. ( Chen, M; Gao, B; Ji, A; Li, H; Li, M; Li, Y; Ma, C; Wang, S; Wu, D; Yao, L, 2016) |
| " We found that obesity in mice reduced the bioavailability of the gaseous signaling molecule hydrogen sulfide (H2S)." | 1.42 | Depletion of H2S during obesity enhances store-operated Ca2+ entry in adipose tissue macrophages to increase cytokine production. ( Beaman, KD; Candela, J; Huang, H; Jaiswal, MK; Prakriya, M; Sun, H; Velmurugan, GV; White, C; Yamashita, M, 2015) |
| "Hydrogen sulfide (H(2)S) has been traditionally known for its toxic effects on living organisms." | 1.35 | Pancreatic islet overproduction of H2S and suppressed insulin release in Zucker diabetic rats. ( Cao, K; Duridanova, D; Jia, X; Wang, R; Wu, L; Yang, G; Yang, W, 2009) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (2.86) | 29.6817 |
| 2010's | 25 (71.43) | 24.3611 |
| 2020's | 9 (25.71) | 2.80 |
| Authors | Studies |
|---|---|
| Bełtowski, J | 5 |
| Wiórkowski, K | 1 |
| Shahi, SK | 1 |
| Ghimire, S | 1 |
| Lehman, P | 1 |
| Mangalam, AK | 1 |
| Zinchuk, VV | 1 |
| Al-Jebur, JSO | 1 |
| Glutkina, NV | 1 |
| Blaha, I | 1 |
| López-Oliva, ME | 1 |
| Martínez, MP | 1 |
| Recio, P | 1 |
| Agis-Torres, Á | 1 |
| Martínez, AC | 1 |
| Benedito, S | 1 |
| García-Sacristán, A | 1 |
| Prieto, D | 1 |
| Fernandes, VS | 1 |
| Hernández, M | 1 |
| Han, L | 1 |
| Wu, G | 2 |
| Feng, C | 1 |
| Yang, Y | 4 |
| Li, B | 1 |
| Ge, Y | 1 |
| Jiang, Y | 1 |
| Shi, Y | 2 |
| Le, G | 2 |
| Jeddi, S | 2 |
| Gheibi, S | 2 |
| Kashfi, K | 2 |
| Carlström, M | 1 |
| Ghasemi, A | 2 |
| Ortiz-Barrios, M | 1 |
| Gul, M | 1 |
| López-Meza, P | 1 |
| Yucesan, M | 1 |
| Navarro-Jiménez, E | 1 |
| Khuntia, HK | 1 |
| Chanakya, HN | 1 |
| D'Arienzo, M | 1 |
| Coniglio, A | 1 |
| Boag, AM | 1 |
| Short, A | 1 |
| Kennedy, LJ | 1 |
| Syme, H | 1 |
| Graham, PA | 1 |
| Catchpole, B | 1 |
| Tofighi, B | 1 |
| El Shahawy, O | 1 |
| Segoshi, A | 1 |
| Moreno, KP | 1 |
| Badiei, B | 1 |
| Sarker, A | 1 |
| Krawczyk, N | 1 |
| Zhou, Y | 2 |
| Li, R | 1 |
| Guo, B | 1 |
| Zhang, L | 1 |
| Zhang, H | 1 |
| Xia, S | 1 |
| Liu, Y | 2 |
| Nielsen, CU | 1 |
| Pedersen, M | 1 |
| Müller, S | 1 |
| Kæstel, T | 1 |
| Bjerg, M | 1 |
| Ulaganathan, N | 1 |
| Nielsen, S | 1 |
| Carlsen, KL | 1 |
| Nøhr, MK | 1 |
| Holm, R | 1 |
| Dottino, JA | 1 |
| Zhang, Q | 2 |
| Loose, DS | 1 |
| Fellman, B | 1 |
| Melendez, BD | 1 |
| Borthwick, MS | 1 |
| McKenzie, LJ | 1 |
| Yuan, Y | 1 |
| Yang, RK | 1 |
| Broaddus, RR | 1 |
| Lu, KH | 1 |
| Soliman, PT | 1 |
| Yates, MS | 1 |
| Zhu, Z | 1 |
| Hasegawa, K | 1 |
| Ma, B | 1 |
| Fujiogi, M | 1 |
| Camargo, CA | 1 |
| Liang, L | 1 |
| Sangroula, S | 1 |
| Baez Vasquez, AY | 1 |
| Raut, P | 1 |
| Obeng, B | 1 |
| Shim, JK | 1 |
| Bagley, GD | 1 |
| West, BE | 1 |
| Burnell, JE | 1 |
| Kinney, MS | 1 |
| Potts, CM | 1 |
| Weller, SR | 1 |
| Kelley, JB | 1 |
| Hess, ST | 1 |
| Gosse, JA | 1 |
| Breves, JP | 1 |
| Springer-Miller, RH | 1 |
| Chenoweth, DA | 1 |
| Paskavitz, AL | 1 |
| Chang, AYH | 1 |
| Regish, AM | 1 |
| Einarsdottir, IE | 1 |
| Björnsson, BT | 1 |
| McCormick, SD | 1 |
| Villmones, HC | 1 |
| Halland, A | 1 |
| Stenstad, T | 1 |
| Ulvestad, E | 1 |
| Weedon-Fekjær, H | 1 |
| Kommedal, Ø | 1 |
| Nasri, A | 1 |
| Jaleh, B | 1 |
| Khazalpour, S | 1 |
| Nasrollahzadeh, M | 1 |
| Shokouhimehr, M | 1 |
| Ferrario, M | 1 |
| Fenoglio, D | 1 |
| Chantada, A | 1 |
| Guerrero, S | 1 |
| Odetayo, AA | 1 |
| Reible, DD | 1 |
| Acevedo-Mackey, D | 1 |
| Price, C | 1 |
| Thai, L | 1 |
| Li, S | 1 |
| Lin, Y | 1 |
| Wang, D | 1 |
| Zhang, C | 1 |
| Wang, Z | 1 |
| Li, X | 1 |
| Chen, Y | 3 |
| Nie, E | 1 |
| Huang, L | 1 |
| Lu, Y | 2 |
| Gao, X | 1 |
| Akhtar, K | 1 |
| Ye, Q | 1 |
| Wang, H | 2 |
| Li, Y | 2 |
| Wang, M | 1 |
| Chen, W | 1 |
| Dai, Y | 2 |
| Guo, X | 1 |
| An, Y | 1 |
| Chai, C | 1 |
| Sang, J | 1 |
| Jiang, L | 1 |
| Lu, F | 1 |
| Liu, F | 1 |
| Pu, Y | 1 |
| Zhou, B | 1 |
| Xiang, H | 1 |
| Wu, W | 1 |
| Yin, H | 1 |
| Yue, W | 1 |
| Yin, Y | 1 |
| Li, H | 2 |
| Xu, H | 1 |
| Shaw, L | 1 |
| Shaw, D | 1 |
| Hardisty, M | 1 |
| Britz-McKibbin, P | 1 |
| Verma, DK | 1 |
| Li, W | 1 |
| Wufuer, R | 1 |
| Duo, J | 1 |
| Wang, S | 2 |
| Luo, Y | 1 |
| Zhang, D | 1 |
| Pan, X | 1 |
| Jones, DL | 1 |
| Baluja, MQ | 1 |
| Graham, DW | 1 |
| Corbishley, A | 1 |
| McDonald, JE | 1 |
| Malham, SK | 1 |
| Hillary, LS | 1 |
| Connor, TR | 1 |
| Gaze, WH | 1 |
| Moura, IB | 1 |
| Wilcox, MH | 1 |
| Farkas, K | 1 |
| Liu, X | 1 |
| Wang, J | 2 |
| Shao, X | 1 |
| Liu, J | 1 |
| Ji, X | 1 |
| Tian, G | 1 |
| Zhang, Y | 2 |
| Sun, R | 1 |
| Wang, L | 1 |
| Zhu, Y | 1 |
| Tuyiringire, D | 1 |
| Li, K | 1 |
| Han, W | 1 |
| Wang, Y | 3 |
| Yan, L | 1 |
| El Hayany, B | 1 |
| El Fels, L | 1 |
| Quénéa, K | 1 |
| Dignac, MF | 1 |
| Rumpel, C | 1 |
| Gupta, VK | 1 |
| Hafidi, M | 1 |
| de Oliveira, BR | 1 |
| Bragança, MLBM | 1 |
| Batalha, MA | 1 |
| Coelho, CCNDS | 1 |
| Bettiol, H | 1 |
| Barbieri, MA | 1 |
| Saraiva, MDCP | 1 |
| Kac, G | 1 |
| da Silva, AAM | 1 |
| Rather, BA | 1 |
| Mir, IR | 1 |
| Sehar, Z | 1 |
| Anjum, NA | 1 |
| Masood, A | 1 |
| Khan, NA | 1 |
| Songsamoe, S | 1 |
| Koomhin, P | 1 |
| Matan, N | 1 |
| Flögel, F | 1 |
| Gärtner, S | 1 |
| Rahimi Khonakdari, M | 1 |
| Rezadoost, H | 1 |
| Heydari, R | 1 |
| Mirjalili, MH | 1 |
| Kebaili, I | 1 |
| Boukhris, I | 1 |
| Sayyed, MI | 1 |
| Tonguc, B | 1 |
| Al-Buriahi, MS | 1 |
| Ganson, KT | 1 |
| Nagata, JM | 1 |
| Cole, MA | 2 |
| Ozgen, C | 1 |
| Strobl, E | 1 |
| Coker, ES | 1 |
| Cavalli, L | 1 |
| Fabrizi, E | 1 |
| Guastella, G | 1 |
| Lippo, E | 1 |
| Parisi, ML | 1 |
| Pontarollo, N | 1 |
| Rizzati, M | 1 |
| Varacca, A | 1 |
| Vergalli, S | 1 |
| Elliott, RJR | 1 |
| Liu, B | 1 |
| Bajelan, S | 1 |
| Bahreini, MS | 1 |
| Asgari, Q | 1 |
| Mikaeili, F | 1 |
| Lakmal, MAC | 1 |
| Ekanayake, EMDNK | 1 |
| Kelum, SHP | 1 |
| Gamage, BD | 1 |
| Jayasundara, JASB | 1 |
| Gautam, S | 1 |
| Gautam, A | 1 |
| Chhetri, S | 1 |
| Bhattarai, U | 1 |
| Acharjee, N | 1 |
| Patel, AK | 1 |
| Lodha, D | 1 |
| Shekhawat, NS | 1 |
| Zeng, W | 1 |
| Dong, A | 1 |
| Chen, X | 1 |
| Cheng, ZL | 1 |
| Campo, M | 1 |
| Amandi, A | 1 |
| Biset, JC | 1 |
| Roviello, V | 1 |
| Roviello, GN | 1 |
| Lee, HJ | 1 |
| Mariappan, MM | 1 |
| Norton, L | 1 |
| Bakewell, T | 1 |
| Feliers, D | 1 |
| Oh, SB | 1 |
| Donati, A | 1 |
| Rubannelsonkumar, CS | 1 |
| Venkatachalam, MA | 1 |
| Harris, SE | 1 |
| Rubera, I | 1 |
| Tauc, M | 1 |
| Ghosh Choudhury, G | 1 |
| Kahn, CR | 1 |
| Sharma, K | 1 |
| DeFronzo, RA | 1 |
| Kasinath, BS | 1 |
| Ren, H | 1 |
| Liu, TC | 1 |
| Zhang, K | 1 |
| Xu, Y | 2 |
| Zhou, P | 1 |
| Tang, X | 1 |
| Candela, J | 3 |
| Wang, R | 2 |
| White, C | 3 |
| Sun, X | 1 |
| Zeng, Q | 2 |
| Huang, X | 1 |
| Cai, J | 3 |
| Zhao, H | 1 |
| Lu, S | 1 |
| Chai, J | 1 |
| Ma, X | 1 |
| Chen, J | 1 |
| Guan, Q | 1 |
| Wan, M | 1 |
| Sandu, RE | 1 |
| Dumbrava, D | 1 |
| Surugiu, R | 1 |
| Glavan, DG | 1 |
| Gresita, A | 1 |
| Petcu, EB | 1 |
| Zheng, F | 1 |
| Han, J | 1 |
| Lu, H | 1 |
| Cui, C | 1 |
| Yang, J | 3 |
| Cui, Q | 2 |
| Tang, C | 3 |
| Xu, G | 2 |
| Geng, B | 3 |
| Sun, J | 1 |
| Luo, T | 1 |
| Cai, B | 1 |
| Liao, F | 1 |
| Zheng, Y | 1 |
| Fan, X | 1 |
| Gong, Y | 1 |
| Cui, QH | 1 |
| Xu, GH | 1 |
| Jamroz-Wiśniewska, A | 3 |
| Gertler, A | 1 |
| Solomon, G | 1 |
| Wood, ME | 1 |
| Whiteman, M | 2 |
| Song, P | 1 |
| Zou, MH | 1 |
| Helmy, N | 1 |
| Prip-Buus, C | 1 |
| Vons, C | 1 |
| Lenoir, V | 1 |
| Abou-Hamdan, A | 1 |
| Guedouari-Bounihi, H | 1 |
| Lombès, A | 1 |
| Bouillaud, F | 1 |
| Guranowski, A | 1 |
| Wolski, A | 1 |
| Hałas, K | 1 |
| Carter, RN | 1 |
| Morton, NM | 1 |
| Velmurugan, GV | 2 |
| Huang, H | 1 |
| Sun, H | 1 |
| Jaiswal, MK | 1 |
| Beaman, KD | 1 |
| Yamashita, M | 1 |
| Prakriya, M | 1 |
| Shi, X | 1 |
| Fan, J | 1 |
| Feng, Y | 1 |
| Lin, X | 1 |
| Jenkins, TA | 1 |
| Nguyen, JC | 1 |
| Hart, JL | 1 |
| Wu, D | 1 |
| Gao, B | 1 |
| Li, M | 1 |
| Yao, L | 1 |
| Chen, M | 1 |
| Ma, C | 1 |
| Ji, A | 1 |
| Nikonorova, IA | 1 |
| Al-Baghdadi, RJT | 1 |
| Mirek, ET | 1 |
| Goudie, MP | 1 |
| Wetstein, BB | 1 |
| Dixon, JL | 1 |
| Hine, C | 1 |
| Mitchell, JR | 1 |
| Adams, CM | 1 |
| Wek, RC | 1 |
| Anthony, TG | 1 |
| Wu, L | 2 |
| Yang, W | 1 |
| Jia, X | 1 |
| Yang, G | 1 |
| Duridanova, D | 1 |
| Cao, K | 1 |
| Gooding, KM | 1 |
| Whatmore, JL | 1 |
| Ball, CI | 1 |
| Mawson, D | 1 |
| Skinner, K | 1 |
| Tooke, JE | 1 |
| Shore, AC | 1 |
| Desai, KM | 1 |
| Chang, T | 1 |
| Untereiner, A | 1 |
| Huang, CY | 1 |
| Yao, WF | 1 |
| Wu, WG | 1 |
| Lu, YL | 1 |
| Wan, H | 1 |
| Wang, W | 1 |
7 reviews available for hydrogen sulfide and Obesity
| Article | Year |
|---|---|
Effect of 12-week of aerobic exercise on hormones and lipid profile status in adolescent girls with polycystic ovary syndrome: A study during COVID-19.
Topics: Actin Cytoskeleton; Actins; Adaptor Proteins, Signal Transducing; Adenocarcinoma; Adenosine Triphosp | 2023 |
Topics: Acyclic Monoterpenes; Adipose Tissue; Adolescent; Adult; Aged; Aged, 80 and over; Air Pollutants; Ai | 2020 |
Topics: Acyclic Monoterpenes; Adipose Tissue; Adolescent; Adult; Aged; Aged, 80 and over; Air Pollutants; Ai | 2020 |
Topics: Acyclic Monoterpenes; Adipose Tissue; Adolescent; Adult; Aged; Aged, 80 and over; Air Pollutants; Ai | 2020 |
Topics: Acyclic Monoterpenes; Adipose Tissue; Adolescent; Adult; Aged; Aged, 80 and over; Air Pollutants; Ai | 2020 |
Cellular and Molecular Mechanisms Underlying Non-Pharmaceutical Ischemic Stroke Therapy in Aged Subjects.
Topics: Animals; Brain Ischemia; Caloric Restriction; Comorbidity; Diabetes Mellitus; Diet, High-Fat; Diseas | 2017 |
Endogenous hydrogen sulfide in perivascular adipose tissue: role in the regulation of vascular tone in physiology and pathology.
Topics: Adipose Tissue; Animals; Cannabinoids; Cardiovascular Physiological Phenomena; Humans; Hydrogen Sulf | 2013 |
Cysteine and hydrogen sulphide in the regulation of metabolism: insights from genetics and pharmacology.
Topics: Adipose Tissue; Animals; Blood Glucose; Cysteine; Diabetes Mellitus, Type 2; Disease Models, Animal; | 2016 |
Hydrogen Sulfide in the Adipose Tissue-Physiology, Pathology and a Target for Pharmacotherapy.
Topics: Adipocytes; Adipogenesis; Adipose Tissue; Glucose; Humans; Hydrogen Sulfide; Hyperglycemia; Insulin | 2016 |
Hydrogen sulfide and the metabolic syndrome.
Topics: Animals; Blood Glucose; Diabetes Mellitus, Type 2; Humans; Hydrogen Sulfide; Hypertension; Metabolic | 2011 |
1 trial available for hydrogen sulfide and Obesity
| Article | Year |
|---|---|
Effect of 12-week of aerobic exercise on hormones and lipid profile status in adolescent girls with polycystic ovary syndrome: A study during COVID-19.
Topics: Actin Cytoskeleton; Actins; Adaptor Proteins, Signal Transducing; Adenocarcinoma; Adenosine Triphosp | 2023 |
28 other studies available for hydrogen sulfide and Obesity
| Article | Year |
|---|---|
Role of Hydrogen Sulfide and Polysulfides in the Regulation of Lipolysis in the Adipose Tissue: Possible Implications for the Pathogenesis of Metabolic Syndrome.
Topics: Adipose Tissue; Animals; Cyclic GMP; Fatty Acids, Nonesterified; Hydrogen Sulfide; Lipolysis; Male; | 2022 |
Obesity induced gut dysbiosis contributes to disease severity in an animal model of multiple sclerosis.
Topics: Animals; Diet, High-Fat; Disease Models, Animal; Dysbiosis; Encephalomyelitis, Autoimmune, Experimen | 2022 |
Oxygen-binding properties of blood in insulin resistance with different asprosin content.
Topics: Adipokines; Adult; Fibrillin-1; Humans; Hydrogen Sulfide; Insulin Resistance; Male; Middle Aged; Nit | 2023 |
Bladder Dysfunction in an Obese Zucker Rat: The Role of TRPA1 Channels, Oxidative Stress, and Hydrogen Sulfide.
Topics: Animals; Cystathionine beta-Synthase; Cystathionine gamma-Lyase; Hydrogen Sulfide; Insulin Resistanc | 2019 |
Dietary methionine restriction improves the impairment of cardiac function in middle-aged obese mice.
Topics: Animals; Body Weight; Cardiomegaly; Diet; Energy Metabolism; Homocysteine; Hydrogen Sulfide; Male; M | 2020 |
Protective effect of intermediate doses of hydrogen sulfide against myocardial ischemia-reperfusion injury in obese type 2 diabetic rats.
Topics: Animals; Cardiotonic Agents; Diabetes Mellitus, Experimental; Diabetes Mellitus, Type 2; Diet, High- | 2020 |
Proximal tubular epithelial insulin receptor mediates high-fat diet-induced kidney injury.
Topics: Animals; Diet, High-Fat; Epithelium; Female; Hydrogen Sulfide; Insulin Resistance; Kidney Cortex; Ki | 2021 |
A comparison study of the influence of milk protein versus whey protein in high-protein diets on adiposity in rats.
Topics: Activating Transcription Factor 4; Adipose Tissue; Adiposity; Animals; Antioxidants; Body Weight; Di | 2021 |
Microvascular Endothelial Dysfunction in Obesity Is Driven by Macrophage-Dependent Hydrogen Sulfide Depletion.
Topics: Adipose Tissue; Animals; Arterioles; Cell Communication; Coculture Techniques; Cystathionine gamma-L | 2017 |
Reduction of leukocyte-derived H
Topics: Adult; Aged; Blood Glucose; Cholesterol, HDL; Cystathionine gamma-Lyase; Down-Regulation; Female; Gl | 2017 |
Hydrogen sulfide improves diabetic wound healing in ob/ob mice via attenuating inflammation.
Topics: Adult; Animals; Case-Control Studies; Humans; Hydrogen Sulfide; Inflammation; Male; Mice; Mice, Inbr | 2017 |
Cystathionine beta synthase-hydrogen sulfide system in paraventricular nucleus reduced high fatty diet induced obesity and insulin resistance by brain-adipose axis.
Topics: Animals; Cells, Cultured; Corticotropin-Releasing Hormone; Cystathionine beta-Synthase; Diet, High-F | 2018 |
Dietary Methionine Restriction Upregulates Endogenous H
Topics: Animals; Body Composition; Body Weight; Cystathionine gamma-Lyase; Diet, High-Fat; Disease Models, A | 2019 |
Effects of Hydrogen Sulfide on Carbohydrate Metabolism in Obese Type 2 Diabetic Rats.
Topics: Animals; Blood Glucose; Blood Pressure; Carbohydrate Metabolism; Diabetes Mellitus, Experimental; Di | 2019 |
Increase or decrease hydrogen sulfide exert opposite lipolysis, but reduce global insulin resistance in high fatty diet induced obese mice.
Topics: Adipocytes; Alkynes; Animals; Blood Glucose; Carrier Proteins; Cystathionine gamma-Lyase; Cysteine; | 2013 |
Leptin-induced endothelium-dependent vasorelaxation of peripheral arteries in lean and obese rats: role of nitric oxide and hydrogen sulfide.
Topics: Adipose Tissue; Alkynes; Animals; Biological Factors; Bismuth; Cystathionine gamma-Lyase; Diet; Endo | 2014 |
Redox regulation of endothelial cell fate.
Topics: Animals; Apoptosis; Cardiovascular Diseases; Cell Cycle; Cell Movement; Cell Transdifferentiation; C | 2014 |
Oxidation of hydrogen sulfide by human liver mitochondria.
Topics: Blood Pressure; Humans; Hydrogen Sulfide; Mitochondria, Liver; Models, Biological; Obesity; Oxidatio | 2014 |
Hydrogen-sulfide-mediated vasodilatory effect of nucleoside 5'-monophosphorothioates in perivascular adipose tissue.
Topics: Adenosine Monophosphate; Adipose Tissue; Animals; Aorta; Aorta, Abdominal; Aorta, Thoracic; Guanosin | 2015 |
Depletion of H2S during obesity enhances store-operated Ca2+ entry in adipose tissue macrophages to increase cytokine production.
Topics: Adipose Tissue; Animals; Calcium Channels; Calcium Signaling; Cell Line; Cytokines; Hydrogen Sulfide | 2015 |
Cystathionine γ lyase-hydrogen sulfide increases peroxisome proliferator-activated receptor γ activity by sulfhydration at C139 site thereby promoting glucose uptake and lipid storage in adipocytes.
Topics: 3T3-L1 Cells; Adipocytes; Adipogenesis; Animals; Anti-Obesity Agents; Cystathionine gamma-Lyase; Cys | 2016 |
Hydrogen sulfide depletion contributes to microvascular remodeling in obesity.
Topics: Alkynes; Animals; Arterioles; Cells, Cultured; Collagen; Collagenases; Cystathionine gamma-Lyase; Di | 2016 |
Decreased vascular H2S production is associated with vascular oxidative stress in rats fed a high-fat western diet.
Topics: Animals; Aorta; Cystathionine gamma-Lyase; Diet, High-Fat; Diet, Western; Disease Models, Animal; Do | 2016 |
Hydrogen Sulfide Mitigates Kidney Injury in High Fat Diet-Induced Obese Mice.
Topics: Acute Kidney Injury; Animals; Diet, High-Fat; Hydrogen Sulfide; Male; Mice; Mice, Inbred C57BL; Mice | 2016 |
Obesity challenges the hepatoprotective function of the integrated stress response to asparaginase exposure in mice.
Topics: Activating Transcription Factor 4; Activating Transcription Factors; Animals; Apolipoprotein B-100; | 2017 |
Pancreatic islet overproduction of H2S and suppressed insulin release in Zucker diabetic rats.
Topics: Alkynes; Animals; Blood Glucose; Catalysis; Cystathionine gamma-Lyase; Diabetes Mellitus; Glycine; H | 2009 |
Adiposity is a major determinant of plasma levels of the novel vasodilator hydrogen sulphide.
Topics: Adiposity; Adult; Aged; Blood Pressure; Diabetes Mellitus, Type 2; Humans; Hydrogen Sulfide; Insulin | 2010 |
Endogenous CSE/H2 S system mediates TNF-α-induced insulin resistance in 3T3-L1 adipocytes.
Topics: 3T3-L1 Cells; Adipocytes; Animals; Cystathionine gamma-Lyase; Diabetes Mellitus, Type 2; Glucose; Hu | 2013 |