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Pregled bibliografske jedinice broj: 977772

Molecular mechanisms involved in pulmonary arterial hypertension development


Manojlović, Dragan; Drenjančević, Ines
Molecular mechanisms involved in pulmonary arterial hypertension development // Periodicum biologorum, 113 (2011), 3; 327-333 (međunarodna recenzija, pregledni rad, znanstveni)


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Naslov
Molecular mechanisms involved in pulmonary arterial hypertension development

Autori
Manojlović, Dragan ; Drenjančević, Ines

Izvornik
Periodicum biologorum (0031-5362) 113 (2011), 3; 327-333

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, pregledni rad, znanstveni

Ključne riječi
Pulmonary arterial hypertension (PAH), leukotrienes, NO

Sažetak
Pulmonary arterial hypertension (PAH) is an elevation in pulmonary arterial pressure, characterized by symptoms of dyspnea, chest pain, decrease in exercise tolerance-fatigue, syncope and, if untreated, PAH leads to right heart failure. In PAH, there is an imbalance between mediators of vasodilation and vasoconstriction (e.g. nitric oxide and prostacycline – potent vasodilators, platelet inhibitor and antimitogens are decreased in PAH, while thromboxane, vasoconstrictor and platelet activator is increased in PAH, resulting in smooth muscle hypertrophy of small vessels, adventitial and intimal proliferation, and plexiform vascular lesions with vascular thrombosis). Standard diagnostic procedures for PAH include physical examination, pulmonary function testing, radiographic imaging, transthoracic echocardiography, right heart catheterization. Current drugs include synthet c prostanoids (iloprost, epoprostenil, beraprost, treprostinil) – vasodilators and antiplatelet agents. Phosphodiesterase-5 inhibitors decrease the breakdown of cGMP, increasing its intracellular levels, leukotriene receptor antagonist, – zafirlukast, decreases pulmonary arterial and venous pressure. Endothelin receptor blockers, bosentan, decrease pulmonary vascular resistance and improve results of functional tests. Other treatments are: anticoagulants, calcium-channel blockers, positive airway pressure therapy for obstructive sleep apnea, or oxygen for hypoxemia, and surgery. In conclusion, although there are some promising drugs in therapy of PAH, there is a need to develop new ones, together with surgical approaches, in order to increase the survival of patients with PAH. Gene and cell therapy could be expected as future perspectives.

Izvorni jezik
Engleski

Znanstvena područja
Temeljne medicinske znanosti, Kliničke medicinske znanosti



POVEZANOST RADA


Ustanove:
Medicinski fakultet, Osijek

Profili:

Avatar Url Ines Drenjančević (autor)

Citiraj ovu publikaciju:

Manojlović, Dragan; Drenjančević, Ines
Molecular mechanisms involved in pulmonary arterial hypertension development // Periodicum biologorum, 113 (2011), 3; 327-333 (međunarodna recenzija, pregledni rad, znanstveni)
Manojlović, D. & Drenjančević, I. (2011) Molecular mechanisms involved in pulmonary arterial hypertension development. Periodicum biologorum, 113 (3), 327-333.
@article{article, author = {Manojlovi\'{c}, Dragan and Drenjan\v{c}evi\'{c}, Ines}, year = {2011}, pages = {327-333}, keywords = {Pulmonary arterial hypertension (PAH), leukotrienes, NO}, journal = {Periodicum biologorum}, volume = {113}, number = {3}, issn = {0031-5362}, title = {Molecular mechanisms involved in pulmonary arterial hypertension development}, keyword = {Pulmonary arterial hypertension (PAH), leukotrienes, NO} }
@article{article, author = {Manojlovi\'{c}, Dragan and Drenjan\v{c}evi\'{c}, Ines}, year = {2011}, pages = {327-333}, keywords = {Pulmonary arterial hypertension (PAH), leukotrienes, NO}, journal = {Periodicum biologorum}, volume = {113}, number = {3}, issn = {0031-5362}, title = {Molecular mechanisms involved in pulmonary arterial hypertension development}, keyword = {Pulmonary arterial hypertension (PAH), leukotrienes, NO} }

Časopis indeksira:


  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus





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