chloroquine has been researched along with Pulmonary Hypertension in 8 studies
Chloroquine: The prototypical antimalarial agent with a mechanism that is not well understood. It has also been used to treat rheumatoid arthritis, systemic lupus erythematosus, and in the systemic therapy of amebic liver abscesses.
chloroquine : An aminoquinoline that is quinoline which is substituted at position 4 by a [5-(diethylamino)pentan-2-yl]amino group at at position 7 by chlorine. It is used for the treatment of malaria, hepatic amoebiasis, lupus erythematosus, light-sensitive skin eruptions, and rheumatoid arthritis.
Excerpt | Relevance | Reference |
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" The purpose of this study was to investigate whether chloroquine induced relaxation in the pulmonary artery (PA) and attenuates hypoxia-induced pulmonary hypertension (HPH)." | 7.85 | Chloroquine is a potent pulmonary vasodilator that attenuates hypoxia-induced pulmonary hypertension. ( Ayon, RJ; Balistrieri, A; Black, SM; Garcia, JGN; Gu, Y; Liang, Z; Lu, W; Makino, A; McDermott, KM; Song, S; Tang, H; Wang, C; Wang, J; Wang, Z; Wu, K; Wu, X; Yuan, JX; Zhang, Q, 2017) |
"Chloroquine treatment increased whole lung and PASMC p62 protein levels consistent with inhibition of autophagy, and increased levels of BMPR-II protein." | 5.39 | Chloroquine prevents progression of experimental pulmonary hypertension via inhibition of autophagy and lysosomal bone morphogenetic protein type II receptor degradation. ( Dunmore, BJ; Long, L; Lu, J; Marciniak, SJ; Morrell, NW; Southwood, M; Yang, X, 2013) |
" The purpose of this study was to investigate whether chloroquine induced relaxation in the pulmonary artery (PA) and attenuates hypoxia-induced pulmonary hypertension (HPH)." | 3.85 | Chloroquine is a potent pulmonary vasodilator that attenuates hypoxia-induced pulmonary hypertension. ( Ayon, RJ; Balistrieri, A; Black, SM; Garcia, JGN; Gu, Y; Liang, Z; Lu, W; Makino, A; McDermott, KM; Song, S; Tang, H; Wang, C; Wang, J; Wang, Z; Wu, K; Wu, X; Yuan, JX; Zhang, Q, 2017) |
"Chloroquine treatment increased whole lung and PASMC p62 protein levels consistent with inhibition of autophagy, and increased levels of BMPR-II protein." | 1.39 | Chloroquine prevents progression of experimental pulmonary hypertension via inhibition of autophagy and lysosomal bone morphogenetic protein type II receptor degradation. ( Dunmore, BJ; Long, L; Lu, J; Marciniak, SJ; Morrell, NW; Southwood, M; Yang, X, 2013) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 7 (87.50) | 24.3611 |
2020's | 1 (12.50) | 2.80 |
Authors | Studies |
---|---|
Ishikawa, T | 1 |
Abe, K | 1 |
Takana-Ishikawa, M | 1 |
Yoshida, K | 1 |
Watanabe, T | 1 |
Imakiire, S | 1 |
Hosokawa, K | 1 |
Hirano, M | 1 |
Hirano, K | 1 |
Tsutsui, H | 1 |
Wu, K | 1 |
Zhang, Q | 1 |
Wu, X | 1 |
Lu, W | 1 |
Tang, H | 1 |
Liang, Z | 1 |
Gu, Y | 1 |
Song, S | 1 |
Ayon, RJ | 1 |
Wang, Z | 1 |
McDermott, KM | 1 |
Balistrieri, A | 1 |
Wang, C | 1 |
Black, SM | 1 |
Garcia, JGN | 1 |
Makino, A | 1 |
Yuan, JX | 2 |
Wang, J | 1 |
Zhou, Y | 1 |
Wang, Y | 2 |
Wang, X | 1 |
Tian, X | 1 |
Zhang, S | 1 |
Yang, F | 1 |
Guo, H | 1 |
Fan, R | 1 |
Feng, N | 1 |
Jia, M | 1 |
Gu, X | 1 |
Li, J | 1 |
Pei, J | 1 |
Long, L | 1 |
Yang, X | 1 |
Southwood, M | 1 |
Lu, J | 1 |
Marciniak, SJ | 1 |
Dunmore, BJ | 2 |
Morrell, NW | 2 |
Fraidenburg, DR | 1 |
Drake, KM | 1 |
Upton, PD | 1 |
Toshner, MR | 1 |
Aldred, MA | 1 |
Ryan, JJ | 1 |
Teng, RJ | 1 |
Du, J | 1 |
Welak, S | 1 |
Guan, T | 1 |
Eis, A | 1 |
Shi, Y | 1 |
Konduri, GG | 1 |
8 other studies available for chloroquine and Pulmonary Hypertension
Article | Year |
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Chronic Inhibition of Toll-Like Receptor 9 Ameliorates Pulmonary Hypertension in Rats.
Topics: Animals; Antirheumatic Agents; Chloroquine; Disease Models, Animal; Hypertension, Pulmonary; Male; M | 2021 |
Chloroquine is a potent pulmonary vasodilator that attenuates hypoxia-induced pulmonary hypertension.
Topics: Animals; Calcium Channels; Cell Proliferation; Cell Survival; Cells, Cultured; Chloroquine; Humans; | 2017 |
The Protective Effects of Κ-Opioid Receptor Stimulation in Hypoxic Pulmonary Hypertension Involve Inhibition of Autophagy Through the AMPK-MTOR Pathway.
Topics: 3,4-Dichloro-N-methyl-N-(2-(1-pyrrolidinyl)-cyclohexyl)-benzeneacetamide, (trans)-Isomer; AMP-Activa | 2017 |
Chloroquine prevents progression of experimental pulmonary hypertension via inhibition of autophagy and lysosomal bone morphogenetic protein type II receptor degradation.
Topics: Animals; Autophagy; Bone Morphogenetic Protein Receptors, Type II; Cells, Cultured; Chloroquine; Dis | 2013 |
Hungry for more: autophagy in the pathogenesis of pulmonary arterial hypertension.
Topics: Animals; Autophagy; Bone Morphogenetic Protein Receptors, Type II; Chloroquine; Hypertension, Pulmon | 2013 |
The lysosomal inhibitor, chloroquine, increases cell surface BMPR-II levels and restores BMP9 signalling in endothelial cells harbouring BMPR-II mutations.
Topics: Bone Morphogenetic Protein Receptors, Type II; Cell Line; Cell Membrane; Cells, Cultured; Chloroquin | 2013 |
Chloroquine in pulmonary arterial hypertension: a new role for an old drug?
Topics: Animals; Autophagy; Bone Morphogenetic Protein Receptors, Type II; Chloroquine; Hypertension, Pulmon | 2013 |
Cross talk between NADPH oxidase and autophagy in pulmonary artery endothelial cells with intrauterine persistent pulmonary hypertension.
Topics: Adenine; Animals; Apoptosis Regulatory Proteins; Autophagy; Cells, Cultured; Chloroquine; Endothelia | 2012 |