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dimethyl sulfoxide and Primary Peritonitis

dimethyl sulfoxide has been researched along with Primary Peritonitis in 13 studies

Dimethyl Sulfoxide: A highly polar organic liquid, that is used widely as a chemical solvent. Because of its ability to penetrate biological membranes, it is used as a vehicle for topical application of pharmaceuticals. It is also used to protect tissue during CRYOPRESERVATION. Dimethyl sulfoxide shows a range of pharmacological activity including analgesia and anti-inflammation.
dimethyl sulfoxide : A 2-carbon sulfoxide in which the sulfur atom has two methyl substituents.

Research Excerpts

ExcerptRelevanceReference
" Therefore, we evaluated whether the pharmacological properties of 6-gingerol (6G) and 10-gingerol (10G) could modulate AKI and metabolic disruption in a rat model of sepsis (faecal peritonitis)."7.88Gingerol suppresses sepsis-induced acute kidney injury by modulating methylsulfonylmethane and dimethylamine production. ( Brito, GAC; da Silva, JA; de Medeiros, PHQS; Dos Santos, AA; Havt, A; Lima, AÂM; Prata, MMG; Rodrigues, FAP; Santos, ADDC; Santos, TCS; Silveira, ER, 2018)
"The effect of the route of administration of dimethyl sulfoxide on humoral immunity and arthritis was evaluated in the rat model of collagen II autoimmune arthritis."7.67Analysis of dimethyl sulfoxide immunosuppression in the rat model of collagen II autoimmune arthritis: an effect dependent upon intraperitoneal administration and associated with toxicity. ( Cremer, MA; Pinals, RS; Pucevich, CL; Townes, AS; Watson, WC, 1985)
" Therefore, we evaluated whether the pharmacological properties of 6-gingerol (6G) and 10-gingerol (10G) could modulate AKI and metabolic disruption in a rat model of sepsis (faecal peritonitis)."3.88Gingerol suppresses sepsis-induced acute kidney injury by modulating methylsulfonylmethane and dimethylamine production. ( Brito, GAC; da Silva, JA; de Medeiros, PHQS; Dos Santos, AA; Havt, A; Lima, AÂM; Prata, MMG; Rodrigues, FAP; Santos, ADDC; Santos, TCS; Silveira, ER, 2018)
"The changes of plasma dihydrorhodamine 123 oxidation level, the myeloperoxidase activity, and extravasations of Evans blue dye of lung in wild-type mice with or without c-Jun NH2-terminal kinase inhibitor; c-Jun NH2-terminal kinase1 mice and c-Jun NH2-terminal kinase1 mice; and chimeric mice (wild-type --> wild-type, c-Jun NH2-terminal kinase1 --> wild-type) with Pseudomonas aeruginosa-induced peritonitis were determined to evaluate the role of c-Jun NH2-terminal kinase signaling of the hematopoietic cells in peritonitis-induced lung damage."3.76Peritonitis-induced peroxynitrite and lung damage depends on c-Jun NH2-terminal kinase signaling of hematopoietic cells. ( Chen, LW; Chen, PH; Hsu, CM; Tseng, HT, 2010)
"The effect of the route of administration of dimethyl sulfoxide on humoral immunity and arthritis was evaluated in the rat model of collagen II autoimmune arthritis."3.67Analysis of dimethyl sulfoxide immunosuppression in the rat model of collagen II autoimmune arthritis: an effect dependent upon intraperitoneal administration and associated with toxicity. ( Cremer, MA; Pinals, RS; Pucevich, CL; Townes, AS; Watson, WC, 1985)
"The effect of dimexid (dimethylsulfoxide) on kanamycin absorption from the peritoneum was studied on normal albino rats with aseptic peritonitis."3.66[Kanamycin deposition in the peritoneum as affected by dimexide]. ( Aleksevich, IaI; Khomitskiĭ, NV; Rybas', AS; Zverev, VM, 1981)
"Dimethyl sulfoxide (DMSO) is a potent antioxidant which protects against endotoxemia and septic shock in animal models."1.31Therapeutic effect of dimethyl sulfoxide on ICAM-1 gene expression and activation of NF-kappaB and AP-1 in septic rats. ( Albarillo, MV; Chang, CK; Schumer, W, 2001)

Research

Studies (13)

TimeframeStudies, this research(%)All Research%
pre-19907 (53.85)18.7374
1990's1 (7.69)18.2507
2000's2 (15.38)29.6817
2010's3 (23.08)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Rodrigues, FAP1
Santos, ADDC1
de Medeiros, PHQS1
Prata, MMG1
Santos, TCS1
da Silva, JA1
Brito, GAC1
Dos Santos, AA1
Silveira, ER1
Lima, AÂM1
Havt, A1
Huai, W1
Zhao, R1
Song, H1
Zhao, J1
Zhang, L2
Gao, C1
Han, L1
Zhao, W1
Chen, LW1
Tseng, HT1
Chen, PH1
Hsu, CM1
WILLSON, JE1
BROWN, DE1
TIMMENS, EK1
Zverev, VM3
Aleksevich, IaI2
Khomitskiĭ, NV2
Semko, ZV1
Rybas', AS1
Korotkiĭ, VN1
Geleskul, VF1
Kolosovich, IV1
Butyrin, SA1
Chen, YX1
Sato, M1
Watanabe, Y1
Tokui, K1
Kashu, Y1
Kohtani, T1
Nakata, T1
Hamada, Y1
Nezu, K1
Kito, K1
Kawachi, K1
Chang, CK1
Albarillo, MV1
Schumer, W1
Demetriou, AA1
Kagoma, PK1
Kaiser, S1
Seifter, E1
Niu, XT1
Levenson, SM1
Watson, WC1
Pucevich, CL1
Cremer, MA1
Pinals, RS1
Townes, AS1
Moroz, IM1

Other Studies

13 other studies available for dimethyl sulfoxide and Primary Peritonitis

ArticleYear
Gingerol suppresses sepsis-induced acute kidney injury by modulating methylsulfonylmethane and dimethylamine production.
    Scientific reports, 2018, 08-14, Volume: 8, Issue:1

    Topics: Acute Kidney Injury; Animals; Catechols; Dimethyl Sulfoxide; Dimethylamines; Disease Models, Animal;

2018
Aryl hydrocarbon receptor negatively regulates NLRP3 inflammasome activity by inhibiting NLRP3 transcription.
    Nature communications, 2014, Aug-20, Volume: 5

    Topics: Alum Compounds; Animals; Carrier Proteins; Caspase 1; Dimethyl Sulfoxide; Female; Gene Expression Re

2014
Peritonitis-induced peroxynitrite and lung damage depends on c-Jun NH2-terminal kinase signaling of hematopoietic cells.
    Critical care medicine, 2010, Volume: 38, Issue:4

    Topics: Animals; Anthracenes; Blotting, Western; Dimethyl Sulfoxide; Disease Models, Animal; Hematopoiesis;

2010
A TOXICOLOGIC STUDY OF DIMETHYL SULFOXIDE.
    Toxicology and applied pharmacology, 1965, Volume: 7

    Topics: Anemia; Blood Cell Count; Chemical and Drug Induced Liver Injury; Dimethyl Sulfoxide; Dogs; Dyspnea;

1965
[Effects of dimexide on the absorption of penicillin from the abdominal cavity].
    Klinicheskaia khirurgiia, 1984, Issue:1

    Topics: Abdomen; Animals; Dimethyl Sulfoxide; Humans; Penicillins; Peritonitis; Rats

1984
[Kanamycin deposition in the peritoneum as affected by dimexide].
    Antibiotiki, 1981, Volume: 26, Issue:2

    Topics: Absorption; Animals; Dimethyl Sulfoxide; Drug Interactions; Kanamycin; Kinetics; Peritoneum; Periton

1981
[The prevention and treatment of suppurative-septic complications in patients with acute appendicitis].
    Klinicheskaia khirurgiia, 1993, Issue:2

    Topics: Acute Disease; Animals; Anti-Bacterial Agents; Appendicitis; Combined Modality Therapy; Dimethyl Sul

1993
Cryopreserved aortic grafting in the presence of peritonitis.
    Transplantation proceedings, 2000, Volume: 32, Issue:7

    Topics: Animals; Aorta, Abdominal; Cryopreservation; Cryoprotective Agents; Dimethyl Sulfoxide; Graft Surviv

2000
Therapeutic effect of dimethyl sulfoxide on ICAM-1 gene expression and activation of NF-kappaB and AP-1 in septic rats.
    The Journal of surgical research, 2001, Volume: 95, Issue:2

    Topics: Animals; Antioxidants; Cecum; Cell Nucleus; Dimethyl Sulfoxide; Disease Models, Animal; Gene Express

2001
[Intra-abdominal administration of dimexide solutions (DMSO) in the complex treatment of purulent peritonitis].
    Vrachebnoe delo, 1978, Issue:1

    Topics: Dimethyl Sulfoxide; Humans; Injections, Intraperitoneal; Peritonitis

1978
Effect of dimethyl sulfoxide and glycerol on acute bowel ischemia in the rat.
    American journal of surgery, 1985, Volume: 149, Issue:1

    Topics: Animals; Dimethyl Sulfoxide; Glycerol; Hemoperitoneum; Intestinal Obstruction; Ischemia; Male; Mesen

1985
Analysis of dimethyl sulfoxide immunosuppression in the rat model of collagen II autoimmune arthritis: an effect dependent upon intraperitoneal administration and associated with toxicity.
    Agents and actions, 1985, Volume: 17, Issue:1

    Topics: Administration, Topical; Animals; Antibody Formation; Arthritis; Arthritis, Experimental; Autoimmune

1985
[Treatment of acute suppurative peritonitis with dimexide and antibiotics].
    Khirurgiia, 1974, Issue:10

    Topics: Acute Disease; Adult; Anti-Bacterial Agents; Dimethyl Sulfoxide; Drug Therapy, Combination; Female;

1974