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  1. Article: Anti-inflammatory and side effects of cyclooxygenase inhibitors.

    Süleyman, Halis / Demircan, Berna / Karagöz, Yalçin

    Pharmacological reports : PR

    2007  Volume 59, Issue 3, Page(s) 247–258

    Abstract: ... with COX inhibitors is associated with a number of side effects including gastrointestinal erosions, and ... of inflammatory mediator release. Studies have shown that both therapeutic and side effects of NSAIDs are dependent ... on cyclooxygenase (COX) inhibition. COX isoforms have been named constitutive (COX-1) and inducible (COX-2). COX-1 ...

    Abstract Nonsteroidal anti-inflammatory drugs (NSAIDs) are the most commonly used drugs in inflammatory diseases, since they are effective in management of pain, fever, redness, edema arising as a consequence of inflammatory mediator release. Studies have shown that both therapeutic and side effects of NSAIDs are dependent on cyclooxygenase (COX) inhibition. COX isoforms have been named constitutive (COX-1) and inducible (COX-2). COX-1 catalyzes formation of cytoprotective prostaglandins in thrombocytes, vascular endothelium, stomach mucosa, kidneys, pancreas, Langerhans islets, seminal vesicles, and brain. Induction of COX-2 by various growth factors, proinflammatory agents, endotoxins, mitogens, and tumor agents indicates that this isoform may have a role in induction of pathological processes, such as inflammation. It is well known that therapy with COX inhibitors is associated with a number of side effects including gastrointestinal erosions, and renal and hepatic insufficiency. Such critical adverse reactions are mostly dependent on COX-1 inhibition. As a result of research focused on reduction of the adverse effects of NSAIDs, selective COX-2 inhibitors, such as celecoxib and rofecoxib have been developed. However, many data demonstrate that mechanisms of action of these drugs are multidirectional and complex. These drugs or their derivatives, which belong to the same group, have distinct pharmacological effects, side effects and potencies which implies that there may be more than two, five or even tens of COX isoforms.
    MeSH term(s) Animals ; Anti-Inflammatory Agents, Non-Steroidal/adverse effects ; Anti-Inflammatory Agents, Non-Steroidal/classification ; Anti-Inflammatory Agents, Non-Steroidal/pharmacology ; Cyclooxygenase Inhibitors/adverse effects ; Cyclooxygenase Inhibitors/pharmacology ; Gastric Mucosa/drug effects ; Humans ; Naproxen/adverse effects ; Naproxen/pharmacology ; PPAR alpha/physiology ; Salicylates/adverse effects ; Salicylates/pharmacology
    Chemical Substances Anti-Inflammatory Agents, Non-Steroidal ; Cyclooxygenase Inhibitors ; PPAR alpha ; Salicylates ; Naproxen (57Y76R9ATQ)
    Language English
    Publishing date 2007-06-19
    Publishing country Switzerland
    Document type Journal Article ; Review
    ZDB-ID 2186248-5
    ISSN 1734-1140
    ISSN 1734-1140
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Effect of olive leaf phytochemicals on the anti-acetylcholinesterase, anti-cyclooxygenase-2 and ferric reducing antioxidant capacity.

    Romero-Márquez, Jose M / Navarro-Hortal, María D / Forbes-Hernández, Tamara Y / Varela-López, Alfonso / Puentes, Juan G / Sánchez-González, Cristina / Sumalla-Cano, Sandra / Battino, Maurizio / García-Ruiz, Roberto / Sánchez, Sebastián / Quiles, José L

    Food chemistry

    2024  Volume 444, Page(s) 138516

    Abstract: ... Secoiridoids contributed to the cyclooxygenase-2 inhibitory activity and antioxidant capacity. Compounds ... Greece, Portugal, and Morocco was characterized and their anti-cholinergic, anti-inflammatory, and ... that specific compounds within OL extracts contribute to distinct anti-cholinergic, anti-inflammatory, and ...

    Abstract In this study, the phytochemical profile of fifty olive leaves (OL) extracts from Spain, Italy, Greece, Portugal, and Morocco was characterized and their anti-cholinergic, anti-inflammatory, and antioxidant activities were evaluated. Luteolin-7-O-glucoside, isoharmnentin, and apigenin were involved in the acetylcholinesterase (AChE) inhibitory activity, while oleuropein and hydroxytyrosol showed noteworthy potential. Secoiridoids contributed to the cyclooxygenase-2 inhibitory activity and antioxidant capacity. Compounds such as oleuropein, ligstroside and luteolin-7-O-glucoside, may exert an important role in the ferric reducing antioxidant capacity. It should be also highlighted the role of hydroxytyrosol, hydroxycoumarins, and verbascoside concerning the antioxidant activity. This research provides valuable insights and confirms that specific compounds within OL extracts contribute to distinct anti-cholinergic, anti-inflammatory, and anti-oxidative effects.
    MeSH term(s) Antioxidants/chemistry ; Acetylcholinesterase ; Olea/chemistry ; Cyclooxygenase 2 ; Plant Extracts/chemistry ; Iridoids/analysis ; Phytochemicals/analysis ; Plant Leaves/chemistry ; Anti-Inflammatory Agents/pharmacology ; Anti-Inflammatory Agents/analysis ; Cholinergic Antagonists/analysis ; Phenylethyl Alcohol/analogs & derivatives ; Iridoid Glucosides
    Chemical Substances Antioxidants ; oleuropein (2O4553545L) ; Acetylcholinesterase (EC 3.1.1.7) ; Cyclooxygenase 2 (EC 1.14.99.1) ; 3,4-dihydroxyphenylethanol (10597-60-1) ; Plant Extracts ; Iridoids ; Phytochemicals ; Anti-Inflammatory Agents ; Cholinergic Antagonists ; Phenylethyl Alcohol (ML9LGA7468) ; Iridoid Glucosides
    Language English
    Publishing date 2024-01-23
    Publishing country England
    Document type Journal Article
    ZDB-ID 243123-3
    ISSN 1873-7072 ; 0308-8146
    ISSN (online) 1873-7072
    ISSN 0308-8146
    DOI 10.1016/j.foodchem.2024.138516
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Gastrointestinal toxic side effects of nonsteroidal anti-inflammatory drugs and cyclooxygenase-2-specific inhibitors.

    Buttgereit, F / Burmester, G R / Simon, L S

    The American journal of medicine

    2001  Volume 110 Suppl 3A, Page(s) 13S–9S

    Abstract: ... isoforms of cyclooxygenase (COX): COX-1 and COX-2. The inhibition of COX-1 is believed to be responsible ... Conventional nonsteroidal anti-inflammatory drugs (NSAIDs) are commonly used to treat pain and ... inflammation but are frequently associated with gastrointestinal side effects, including life-threatening ...

    Abstract Conventional nonsteroidal anti-inflammatory drugs (NSAIDs) are commonly used to treat pain and inflammation but are frequently associated with gastrointestinal side effects, including life-threatening bleeding or perforation of gastroduodenal ulcers. Conventional NSAIDs are nonselective inhibitors of two isoforms of cyclooxygenase (COX): COX-1 and COX-2. The inhibition of COX-1 is believed to be responsible for inducing mucosal injury primarily by impairing prostaglandin-dependent mucosal protective mechanisms. The latest development in reducing the incidence of ulcers and ulcer complications associated with conventional NSAIDs is the use of recently approved COX-2-specific inhibitors (CSIs). This article critically reviews the data on gastrointestinal toxic side effects for conventional NSAIDs without as well as with prevention therapy. In addition, we compare these data with those for the CSIs, namely, celecoxib and rofecoxib. Finally, we offer recommendations on the clinical use of these drugs, emphasizing the need to balance clinical effectiveness with the avoidance of potential gastrointestinal side effects.
    MeSH term(s) Anti-Inflammatory Agents, Non-Steroidal/adverse effects ; Anti-Ulcer Agents/therapeutic use ; Celecoxib ; Cyclooxygenase 2 ; Cyclooxygenase 2 Inhibitors ; Cyclooxygenase Inhibitors/adverse effects ; Gastric Mucosa/drug effects ; Gastrointestinal Diseases/chemically induced ; Gastrointestinal Diseases/epidemiology ; Gastrointestinal Diseases/prevention & control ; Humans ; Incidence ; Isoenzymes/antagonists & inhibitors ; Lactones/adverse effects ; Membrane Proteins ; Patient Selection ; Practice Guidelines as Topic ; Prostaglandin-Endoperoxide Synthases ; Pyrazoles ; Sulfonamides/adverse effects ; Sulfones
    Chemical Substances Anti-Inflammatory Agents, Non-Steroidal ; Anti-Ulcer Agents ; Cyclooxygenase 2 Inhibitors ; Cyclooxygenase Inhibitors ; Isoenzymes ; Lactones ; Membrane Proteins ; Pyrazoles ; Sulfonamides ; Sulfones ; rofecoxib (0QTW8Z7MCR) ; Cyclooxygenase 2 (EC 1.14.99.1) ; PTGS2 protein, human (EC 1.14.99.1) ; Prostaglandin-Endoperoxide Synthases (EC 1.14.99.1) ; Celecoxib (JCX84Q7J1L)
    Language English
    Publishing date 2001-02-19
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 80015-6
    ISSN 1555-7162 ; 1873-2178 ; 0002-9343 ; 1548-2766
    ISSN (online) 1555-7162 ; 1873-2178
    ISSN 0002-9343 ; 1548-2766
    DOI 10.1016/s0002-9343(00)00728-2
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: Polmacoxib: A Review of the Newer Non-steroidal Anti-inflammatory Drug in Osteoarthritis.

    Easwaran, Raju / Mistry, Urvi K / Bhole, Milind / Peethambaran, Kartik

    Cureus

    2024  Volume 16, Issue 4, Page(s) e58446

    Abstract: ... cyclooxygenase (COX) inhibitors and cyclooxygenase-1 (COX-1) inhibitors are associated with increased ... the gastric mucosa. Cyclooxygenase-2 (COX-2) inhibitors are associated with an increased incidence of adverse ... and productivity. Non-steroidal anti-inflammatory drugs (NSAIDs) are widely used in the management ...

    Abstract Osteoarthritis represents a huge socioeconomic burden and has a significant impact on daily life and productivity. Non-steroidal anti-inflammatory drugs (NSAIDs) are widely used in the management of osteoarthritis to curb inflammation, pain, and stiffness and improve physical function. However, due to the various side effects, most healthcare professionals avoid using NSAIDs for a long period. Nonselective cyclooxygenase (COX) inhibitors and cyclooxygenase-1 (COX-1) inhibitors are associated with increased gastrointestinal adverse effects due to the inhibition of prostaglandins, which are responsible for protecting the gastric mucosa. Cyclooxygenase-2 (COX-2) inhibitors are associated with an increased incidence of adverse cardiovascular effects due to their COX-2 inhibitory activity in the circulatory system. Therefore, there is a need for a newer NSAID that has a better safety profile to be used in osteoarthritis. Polmacoxib is a new, orally active, first-in-class NSAID that is a dual inhibitor of COX-2 and carbonic anhydrase (CA). The dual mode of action exhibited by polmacoxib is expected to minimize adverse cardiovascular effects while achieving maximum effectiveness in inflamed osteoarthritic joints. This article aims to review the pharmacological properties, clinical efficacy, and safety data of polmacoxib in osteoarthritis.
    Language English
    Publishing date 2024-04-17
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 2747273-5
    ISSN 2168-8184
    ISSN 2168-8184
    DOI 10.7759/cureus.58446
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Anti-oxidative, anti-apoptotic, and anti-inflammatory activities of Connarus semidecandrus Jack ethanol extract in UVB-irradiated human keratinocytes.

    Huang, Lei / Kim, Ji Hye / You, Long / Park, Sang Hee / Zhang, Jianmei / Shin, Chae Yun / Sutopo, Natasha Christabella / Byun, Hye-Woo / Omaliss, Keo / Masphal, Kry / Son, Jino / Kim, Ga Ryun / Lee, Byoung-Hee / Kim, Jong-Hoon / Lee, Jongsung / Cho, Jae Youl

    Journal of ethnopharmacology

    2023  Volume 321, Page(s) 117574

    Abstract: ... such as cyclooxygenase-2 (COX-2), tumor necrosis factor-α (TNF-α), interleukin 6 (IL-6), MMP-1, MMP-3, and MMP-9 ... drugs have many shortcomings and side effects. Therefore, natural products are attractive potential ... anti-aging, and anti-apoptotic effects of Cs-EE indicate the compound's potential usefulness ...

    Abstract Ethnopharmacological relevance: Connarus semidecandrus Jack (Family: connaraceae) is a medicinal plant known for its wide distribution throughout Southeast Asia. Renowned for its diverse therapeutic properties, it has been traditionally used for treating fever, skin irritation, and colic.
    Aim of the study: Numerous individuals suffer from skin issues, including wrinkles, hyperpigmentation, and inflammation, due to environmental factors. Although many drugs are available to treat skin problems, chemical drugs have many shortcomings and side effects. Therefore, natural products are attractive potential medicines for alleviating skin troubles. We recently showed that Connarus semidecandrus Jack ethanol extract (Cs-EE) has anti-alopecia potential. This paper aims to explore the potential skin-protective effects and underlying molecular mechanisms of Connarus semidecandrus Jack in UVB-induced human keratinocytes (HaCaT).
    Materials and methods: Before utilization, Cs-EE was dissolved in dimethyl sulfoxide (DMSO) and was preserved at a temperature of -20 °C. The phytochemical constituents of Cs-EE were detected by gas chromatography-mass spectrometry analysis (GC-MS). Sequentially, HaCaT cells were exposed to varying concentrations of Cs-EE prior to ultraviolet B (UVB) irradiation. Evaluations of cellular responses in HaCaT cells, including assessments of cell viability, deoxyribonucleic acid (DNA) damage, and gene and protein expressions, were carried out. To explore the specific signaling pathway involved, we conducted a luciferase assay in addition to validating these pathways using Western blot analysis.
    Results: Nitric oxide (NO) and intracellular reactive oxygen species were decreased. Melanin production through the activation of melanocytes by α-melanocyte-stimulating hormone (MSH) was also inhibited by Cs-EE. Furthermore, the mRNA expression levels of key factors such as cyclooxygenase-2 (COX-2), tumor necrosis factor-α (TNF-α), interleukin 6 (IL-6), MMP-1, MMP-3, and MMP-9 exhibited a remarkable decrease. In addition, the phosphorylation of TAK1 within the signaling cascade exhibited a decline, and the activities of the transcription factor AP-1 were decreased according to a luciferase reporter assay.
    Conclusions: Taken together, these findings suggest that the anti-inflammatory, anti-aging, and anti-apoptotic effects of Cs-EE indicate the compound's potential usefulness as a natural component in pharmaceutical and cosmetic products.
    MeSH term(s) Humans ; Connaraceae ; Ethanol/chemistry ; Plant Extracts/therapeutic use ; Cell Line ; Keratinocytes ; Anti-Inflammatory Agents/therapeutic use ; Ultraviolet Rays/adverse effects ; Inflammation/drug therapy ; Luciferases
    Chemical Substances Ethanol (3K9958V90M) ; Plant Extracts ; Anti-Inflammatory Agents ; Luciferases (EC 1.13.12.-)
    Language English
    Publishing date 2023-12-13
    Publishing country Ireland
    Document type Journal Article
    ZDB-ID 134511-4
    ISSN 1872-7573 ; 0378-8741
    ISSN (online) 1872-7573
    ISSN 0378-8741
    DOI 10.1016/j.jep.2023.117574
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  6. Article ; Online: Apigenin attenuates indomethacin-induced gastric ulcer in rats: emphasis on antioxidant, anti-inflammatory, anti-apoptotic, and TGF-β1 enhancing activities.

    Alamri, Zaenah Zuhair

    Naunyn-Schmiedeberg's archives of pharmacology

    2024  

    Abstract: ... The gastroprotective effects of apigenin may be attributed to its anti-inflammatory, anti-antioxidant, and anti-apoptotic ... superoxide dismutase (SOD) and catalase, increased the immunoreactivity of the inflammatory markers cyclo-oxygenase-2 ... common causes of the ulcer are Helicobacter pylori infection and non-steroidal anti-inflammatory drugs ...

    Abstract Gastric ulcer disease is associated with significant morbidity and mortality rates. The most two common causes of the ulcer are Helicobacter pylori infection and non-steroidal anti-inflammatory drugs. In the past few decades, a significant decrease in the morbidity and mortality rate has been observed probably due to the discovery of proton pump inhibitors. However, the medications used to treat gastric ulcers impose several nauseous side effects. Therefore, recent studies focus on the use of natural products to treat gastric ulcers. In the current study, gastric ulcer was effectively induced using indomethacin, and the protective effect of apigenin, a potent antioxidant flavonoid, was assessed in comparison to omeprazole. The administration of a single oral indomethacin (50 mg/kg) induced gastric ulcer as manifested by hemorrhagic lesions in the gastric mucosa, increased ulcer index, and histopathological alterations. Indomethacin also increased lipid peroxidation, decreased the activities of the antioxidant enzymes superoxide dismutase (SOD) and catalase, increased the immunoreactivity of the inflammatory markers cyclo-oxygenase-2 (COX-2), tumor necrosis factor-alpha (TNF-α), and nuclear factor-kappa B (NF-κB), increased the transcription of the apoptotic marker, Bax, and decreased that of the antiapoptotic Bcl-2. Indomethacin also decreased the immunoreactivity of transforming growth factor-beta 1 (TGF-β1). On the other hand, pretreatment with apigenin (10 and 20 mg/kg) resulted in a dose-dependent improvement in the macroscopic and microscopic features of the gastric mucosa in a manner comparable to that of omeprazole. The gastroprotective effects of apigenin may be attributed to its anti-inflammatory, anti-antioxidant, and anti-apoptotic activities as well as enhancing the expression of TGF-β1. Further experimental and clinical research is required to confirm activity of apigenin as anti-ulcer agent.
    Language English
    Publishing date 2024-06-06
    Publishing country Germany
    Document type Journal Article
    ZDB-ID 121471-8
    ISSN 1432-1912 ; 0028-1298
    ISSN (online) 1432-1912
    ISSN 0028-1298
    DOI 10.1007/s00210-024-03200-w
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  7. Article: Anti-inflammatoires non stéroïdiens : mise au point pour le praticien.

    Bourdon, Fanny / Buchard, Pierre-Alain / Rodrigues, Bruno / Gobin, Niels

    Revue medicale suisse

    2022  Volume 18, Issue 768, Page(s) 235–240

    Abstract: ... limit their use. Introduction of selective cyclooxygenase-2 inhibitor has provided an alternative to non ... NSAID represent a widely used therapeutic class, but their side- effects profile can significantly ... on their safety profile. Numerous adverse effects, mainly gastrointestinal, renal and cardiovascular, have been ...

    Title translation Non-steroidal anti-inflammatory drugs : clarification for the practitioner.
    Abstract NSAID represent a widely used therapeutic class, but their side- effects profile can significantly limit their use. Introduction of selective cyclooxygenase-2 inhibitor has provided an alternative to non-selective NSAIDs, with a better digestive tolerance for similar efficiency. Nevertheless, introduction of these molecules has been associated with emergence of major cardiovascular events, motivating further studies on their safety profile. Numerous adverse effects, mainly gastrointestinal, renal and cardiovascular, have been more clearly characterized. This article intends to review some of the basic principles and main side effects of NSAIDs.
    MeSH term(s) Anti-Inflammatory Agents, Non-Steroidal/adverse effects ; Cyclooxygenase 2 Inhibitors ; Humans ; Pharmaceutical Preparations
    Chemical Substances Anti-Inflammatory Agents, Non-Steroidal ; Cyclooxygenase 2 Inhibitors ; Pharmaceutical Preparations
    Language French
    Publishing date 2022-02-14
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2177010-4
    ISSN 1660-9379
    ISSN 1660-9379
    DOI 10.53738/REVMED.2022.18.768.235
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  8. Article ; Online: 2-Substituted Benzoxazoles as Potent Anti-Inflammatory Agents: Synthesis, Molecular Docking and In vivo Anti-Ulcerogenic Studies.

    Hamid, Iqra / Nadeem, Humaira / Ansari, Sameen Fatima / Khiljee, Sonia / Abbasi, Inzamam / Bukhari, Asma / Arif, Muazzam / Imran, Muhammad

    Medicinal chemistry (Shariqah (United Arab Emirates))

    2022  Volume 18, Issue 7, Page(s) 791–809

    Abstract: ... Several side effects like gastrointestinal and renal toxicities are associated with the use of these drugs ... anti-inflammatory agents (COX-2 inhibitors). However, further assessments are required to delineate their underlying ... interventions of inflammation and pain that competitively inhibit the cyclooxygenase (COX) enzymes ...

    Abstract Background: Non-steroidal anti-inflammatory drugs (NSAIDs) are the commonly used therapeutic interventions of inflammation and pain that competitively inhibit the cyclooxygenase (COX) enzymes. Several side effects like gastrointestinal and renal toxicities are associated with the use of these drugs. The therapeutic anti-inflammatory benefits of NSAIDs are produced by the inhibition of COX-2 enzymes, while undesirable side effects arise from the inhibition of COX-1 enzymes.
    Objective: In the present study, a new series of 2-substituted benzoxazole derivatives 2(a-f) and 3(ae) were synthesized in our lab as potent anti-inflammatory agents with outstanding gastro-protective potential. The new analogs 2(a-f) and 3(a-e) were designed depending upon the literature review to serve as ligands for the development of selective COX-2 inhibitors.
    Methods: The synthesized analogs were characterized using different spectroscopic techniques (FTIR,
    Results: Five compounds (2a, 2b, 3a, 3b and 3c) exhibited potent anti-inflammatory activity and significant binding potential in the COX-2 protein pocket. Similarly, these five compounds demonstrated a significant gastro-protective effect (**p<0.01) in comparison to the standard drug, Omeprazole.
    Conclusion: Depending upon our results, we hypothesize that 2-substituted benzoxazole derivatives have excellent potential to serve as candidates for the development of selective anti-inflammatory agents (COX-2 inhibitors). However, further assessments are required to delineate their underlying mechanisms.
    MeSH term(s) Animals ; Anti-Inflammatory Agents/pharmacology ; Anti-Inflammatory Agents/therapeutic use ; Anti-Inflammatory Agents, Non-Steroidal/chemistry ; Benzoxazoles/chemistry ; Benzoxazoles/pharmacology ; Benzoxazoles/therapeutic use ; Carrageenan/adverse effects ; Cyclooxygenase 1/metabolism ; Cyclooxygenase 2/metabolism ; Cyclooxygenase 2 Inhibitors/chemistry ; Cyclooxygenase 2 Inhibitors/pharmacology ; Edema/chemically induced ; Edema/drug therapy ; Molecular Docking Simulation ; Rats ; Structure-Activity Relationship ; Ulcer
    Chemical Substances Anti-Inflammatory Agents ; Anti-Inflammatory Agents, Non-Steroidal ; Benzoxazoles ; Cyclooxygenase 2 Inhibitors ; Carrageenan (9000-07-1) ; Cyclooxygenase 1 (EC 1.14.99.1) ; Cyclooxygenase 2 (EC 1.14.99.1)
    Language English
    Publishing date 2022-06-16
    Publishing country Netherlands
    Document type Journal Article
    ISSN 1875-6638
    ISSN (online) 1875-6638
    DOI 10.2174/1573406418666211220125344
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  9. Article ; Online: Involvement of TNFα, IL-1β, COX-2 and NO in the anti-inflammatory activity of Tamarix aphylla in Wistar albino rats: an in-vivo and in-vitro study.

    Fayez, Nada / Khalil, Waleed / Abdel-Sattar, Essam / Abdel-Fattah, Abdel-Fattah Mohamed

    BMC complementary medicine and therapies

    2024  Volume 24, Issue 1, Page(s) 57

    Abstract: ... the anti-inflammatory activity of Tamarix aphylla (TA) and investigate the potential mechanism underlying this action ... Background: With the emergence of many side effects from synthetic drugs, there is an urgent need ... 200 and 400 mg/kg doses significantly (P < 0.05) inhibited the heat-induced hemolysis of RBCs membrane ...

    Abstract Background: With the emergence of many side effects from synthetic drugs, there is an urgent need to find a natural alternative to these products. Therefore, our primary aim was to evaluate the anti-inflammatory activity of Tamarix aphylla (TA) and investigate the potential mechanism underlying this action.
    Methods: Initially, to ensure the safety of the extract and for dose selection, we performed an acute oral toxicity Assay through the oral administration of graded doses up to 4 g\kg in Wistar rats. then, we used the carrageenan-induced edema model to elucidate the anti-inflammatory activity. Using specific ELISA kits, we measured the levels of TNF-α, IL-1β, COX-2 and NO inside the inflamed paw tissue. Finally, for the in-vitro anti-inflammatory experiment, we used the erythrocyte membrane stability test.
    Results: Based on the acute oral toxicity assay, T. aphylla was considered generally safe and three different doses of 100, 200, and 400 mg/kg were chosen for further experiments. Additionally, TA expressed a significant (P < 0.05) anti-inflammatory activity, showing the maximum inhibition percentage at the fifth hour of measurement at 53.47% and 70.06%, at doses of 200 and 400 mg/kg respectively, compared to 63.81% for the standard drug. Similarly, we found that TA effectively reduced the levels of TNF-α and IL-1β at all tested doses (100-200-400 mg/kg) to a greater extent than the standard drug. Moreover, at 400 mg/kg, TA was able to significantly lower the levels of COX-2 and NO inside the inflamed tissue to a level comparable (P < 0.05) with that measured inside the paw tissue of normal rats. Finally, Tamarix aphylla at 100, 200 and 400 mg/kg doses significantly (P < 0.05) inhibited the heat-induced hemolysis of RBCs membrane by 67.78, 74.82 and 82.08%, respectively, compared to 83.89% produced by Aspirin.
    Conclusion: T. aphylla produced a significant (P < 0.05) anti-inflammatory activity compared to the standard drugs either through the reduction of pro-inflammatory mediators or the protection of the lysosomal membrane.
    MeSH term(s) Rats ; Animals ; Tumor Necrosis Factor-alpha ; Rats, Wistar ; Tamaricaceae ; Cyclooxygenase 2 ; Plant Extracts/therapeutic use ; Anti-Inflammatory Agents/therapeutic use
    Chemical Substances Tumor Necrosis Factor-alpha ; Cyclooxygenase 2 (EC 1.14.99.1) ; Plant Extracts ; Anti-Inflammatory Agents
    Language English
    Publishing date 2024-01-25
    Publishing country England
    Document type Journal Article
    ISSN 2662-7671
    ISSN (online) 2662-7671
    DOI 10.1186/s12906-024-04359-8
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  10. Article ; Online: The anti-inflammatory and vasoprotective properties of mPGES-1 inhibition offer promising therapeutic potential.

    Steinmetz-Späh, Julia / Jakobsson, Per-Johan

    Expert opinion on therapeutic targets

    2023  Volume 27, Issue 11, Page(s) 1115–1123

    Abstract: ... anti-inflammatory treatment strategy and beneficial and safer regarding cardiovascular side effects compared ... to NSAIDs. Inhibitors of mPGES-1 hold great potential to advance to the clinic and there are ongoing phase ... and metabolism with a strong focus on the vascular effects of prostanoids. Recent advances in mPGES-1 ...

    Abstract Introduction: Prostaglandin E
    Areas covered: The article briefly describes prostanoid history and metabolism with a strong focus on the vascular effects of prostanoids. Recent advances in mPGES-1 inhibitor development and results from pre-clinical and clinical studies are presented. Prostanoid shunting after mPGES-1 inhibition is highlighted and particularly discussed in the context of cardiovascular diseases.
    Expert opinion: The newest research demonstrates that inhibition of mPGES-1 is a potent anti-inflammatory treatment strategy and beneficial and safer regarding cardiovascular side effects compared to NSAIDs. Inhibitors of mPGES-1 hold great potential to advance to the clinic and there are ongoing phase-II trials in endometriosis.
    MeSH term(s) Female ; Humans ; Prostaglandin-E Synthases/metabolism ; Prostaglandins/metabolism ; Anti-Inflammatory Agents/pharmacology ; Dinoprostone/metabolism ; Anti-Inflammatory Agents, Non-Steroidal/adverse effects ; Cyclooxygenase 2/metabolism
    Chemical Substances Prostaglandin-E Synthases (EC 5.3.99.3) ; Prostaglandins ; Anti-Inflammatory Agents ; Dinoprostone (K7Q1JQR04M) ; Anti-Inflammatory Agents, Non-Steroidal ; Cyclooxygenase 2 (EC 1.14.99.1)
    Language English
    Publishing date 2023-12-07
    Publishing country England
    Document type Journal Article ; Review ; Research Support, Non-U.S. Gov't
    ZDB-ID 2055208-7
    ISSN 1744-7631 ; 1472-8222
    ISSN (online) 1744-7631
    ISSN 1472-8222
    DOI 10.1080/14728222.2023.2285785
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