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The possible role of the seaweed Ulva fasciata on ameliorating hyperthyroidism-associated heart inflammations in a rat model

Cardiovascular diseases are key complications primarily associated with hyperthyroidism disorders. The present study sought to ameliorate hyperthyroidism-mediated cardiovascular inflammations and related oxidative stress paradigms in experimental rats using the broadly distributed green seaweed Ulva...

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Published in:Environmental science and pollution research international 2021-02, Vol.28 (6), p.6830-6842
Main Authors: Ibrahim, Rasha Youssef Mohammed, Saber, Abdullah Antar, Hammad, Huda Badr Ibrahim
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description Cardiovascular diseases are key complications primarily associated with hyperthyroidism disorders. The present study sought to ameliorate hyperthyroidism-mediated cardiovascular inflammations and related oxidative stress paradigms in experimental rats using the broadly distributed green seaweed Ulva fasciata . Forty-eight adult male albino rats were recruited and randomly classified into six groups. Hyperthyroidism was stimulated using l -thyroxine sodium at a dose of 100 μg/kg i.p. for 3 weeks daily. Further, 200 mg/kg b.wt. concentration of the U . fasciata methanolic ( U . fasciata -MeOH) extract was the recommended dose and administrated orally to the hyperthyroid rats. The standard commercial drug “propranolol hydrochloride” was also tested at a dose of 10 mg/kg i.p. to compare the findings obtained from the seaweed extract. A combined treatment with the U . fasciata -MeOH extract and propranolol hydrochloride was also assessed. Our results implied that the treatment of hyperthyroid rats with the U . fasciata -MeOH extract significantly reduced serum levels of the thyroid hormones T3 and T4, proinflammatory cytokines (TNF-α, MPO, and CRP), triglycerides and total cholesterol, as well as the cardiac biomarkers CK-MB, LDH, and troponin to thresholds close to those of the standard drug. In addition, levels of high-density lipoprotein cholesterol (HDL-C) and interleukin 10 (IL-10) were significantly upregulated. Hyperthyroid rats only treated with propranolol hydrochloride, or with a combination of the drug and the seaweed extract, conferred the same observations. Histopathological architecture boosted our interesting findings where the myocardium tissues in hyperthyroid rats, administrated the U . fasciata -MeOH extract or/and propranolol hydrochloride, exhibited more or less a normal structure as the control, reflecting the potential cardiovascular recovery exerted by this seaweed extract. In vitro DPPH, ABTS, and FRAP antioxidant assays of the U . fasciata -MeOH extract showed an outstanding ROS-scavenging potential. HPLC analysis of the U . fasciata -MeOH extract unraveled an inestimable valuable array of phenolics (mainly p -coumaric, gallic, ferulic, chlorogenic, and syringic acids) and flavonoids (hesperidin, kaempferol, catechin, quercetin, and rutin). Conclusively, the seaweed U . fasciata is a profitable source of antioxidant polyphenolics characterized by having a pharmaceutical potential against hyperthyroidism-linked cardiovascular inflammati
doi_str_mv 10.1007/s11356-020-11036-z
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The present study sought to ameliorate hyperthyroidism-mediated cardiovascular inflammations and related oxidative stress paradigms in experimental rats using the broadly distributed green seaweed Ulva fasciata . Forty-eight adult male albino rats were recruited and randomly classified into six groups. Hyperthyroidism was stimulated using l -thyroxine sodium at a dose of 100 μg/kg i.p. for 3 weeks daily. Further, 200 mg/kg b.wt. concentration of the U . fasciata methanolic ( U . fasciata -MeOH) extract was the recommended dose and administrated orally to the hyperthyroid rats. The standard commercial drug “propranolol hydrochloride” was also tested at a dose of 10 mg/kg i.p. to compare the findings obtained from the seaweed extract. A combined treatment with the U . fasciata -MeOH extract and propranolol hydrochloride was also assessed. Our results implied that the treatment of hyperthyroid rats with the U . fasciata -MeOH extract significantly reduced serum levels of the thyroid hormones T3 and T4, proinflammatory cytokines (TNF-α, MPO, and CRP), triglycerides and total cholesterol, as well as the cardiac biomarkers CK-MB, LDH, and troponin to thresholds close to those of the standard drug. In addition, levels of high-density lipoprotein cholesterol (HDL-C) and interleukin 10 (IL-10) were significantly upregulated. Hyperthyroid rats only treated with propranolol hydrochloride, or with a combination of the drug and the seaweed extract, conferred the same observations. Histopathological architecture boosted our interesting findings where the myocardium tissues in hyperthyroid rats, administrated the U . fasciata -MeOH extract or/and propranolol hydrochloride, exhibited more or less a normal structure as the control, reflecting the potential cardiovascular recovery exerted by this seaweed extract. In vitro DPPH, ABTS, and FRAP antioxidant assays of the U . fasciata -MeOH extract showed an outstanding ROS-scavenging potential. HPLC analysis of the U . fasciata -MeOH extract unraveled an inestimable valuable array of phenolics (mainly p -coumaric, gallic, ferulic, chlorogenic, and syringic acids) and flavonoids (hesperidin, kaempferol, catechin, quercetin, and rutin). 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In vitro DPPH, ABTS, and FRAP antioxidant assays of the U . fasciata -MeOH extract showed an outstanding ROS-scavenging potential. HPLC analysis of the U . fasciata -MeOH extract unraveled an inestimable valuable array of phenolics (mainly p -coumaric, gallic, ferulic, chlorogenic, and syringic acids) and flavonoids (hesperidin, kaempferol, catechin, quercetin, and rutin). 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The present study sought to ameliorate hyperthyroidism-mediated cardiovascular inflammations and related oxidative stress paradigms in experimental rats using the broadly distributed green seaweed Ulva fasciata . Forty-eight adult male albino rats were recruited and randomly classified into six groups. Hyperthyroidism was stimulated using l -thyroxine sodium at a dose of 100 μg/kg i.p. for 3 weeks daily. Further, 200 mg/kg b.wt. concentration of the U . fasciata methanolic ( U . fasciata -MeOH) extract was the recommended dose and administrated orally to the hyperthyroid rats. The standard commercial drug “propranolol hydrochloride” was also tested at a dose of 10 mg/kg i.p. to compare the findings obtained from the seaweed extract. A combined treatment with the U . fasciata -MeOH extract and propranolol hydrochloride was also assessed. Our results implied that the treatment of hyperthyroid rats with the U . fasciata -MeOH extract significantly reduced serum levels of the thyroid hormones T3 and T4, proinflammatory cytokines (TNF-α, MPO, and CRP), triglycerides and total cholesterol, as well as the cardiac biomarkers CK-MB, LDH, and troponin to thresholds close to those of the standard drug. In addition, levels of high-density lipoprotein cholesterol (HDL-C) and interleukin 10 (IL-10) were significantly upregulated. Hyperthyroid rats only treated with propranolol hydrochloride, or with a combination of the drug and the seaweed extract, conferred the same observations. Histopathological architecture boosted our interesting findings where the myocardium tissues in hyperthyroid rats, administrated the U . fasciata -MeOH extract or/and propranolol hydrochloride, exhibited more or less a normal structure as the control, reflecting the potential cardiovascular recovery exerted by this seaweed extract. In vitro DPPH, ABTS, and FRAP antioxidant assays of the U . fasciata -MeOH extract showed an outstanding ROS-scavenging potential. HPLC analysis of the U . fasciata -MeOH extract unraveled an inestimable valuable array of phenolics (mainly p -coumaric, gallic, ferulic, chlorogenic, and syringic acids) and flavonoids (hesperidin, kaempferol, catechin, quercetin, and rutin). Conclusively, the seaweed U . fasciata is a profitable source of antioxidant polyphenolics characterized by having a pharmaceutical potential against hyperthyroidism-linked cardiovascular inflammations and oxidative stress patterns due to their substantial free radical quenching properties, and also via regulating the signalling pathways of the proinflammatory, lipid profile, and cardiac biomarkers.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>33011948</pmid><doi>10.1007/s11356-020-11036-z</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0002-4676-6998</orcidid></addata></record>
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source ABI/INFORM Global; Springer Nature
subjects Algae
Animals
Antioxidants
Aquatic Pollution
Atmospheric Protection/Air Quality Control/Air Pollution
Biomarkers
Calcium-binding protein
Cardiovascular diseases
Cardiovascular system
Catechin
Cholesterol
Combined treatment
Cytokines
Drug dosages
Earth and Environmental Science
Ecotoxicology
Environment
Environmental Chemistry
Environmental Health
Environmental science
Flavonoids
Free radicals
Hesperidin
High density lipoprotein
High-performance liquid chromatography
Hormones
Hyperthyroidism
Hyperthyroidism - drug therapy
Inflammation
Inflammation - drug therapy
Interleukin 10
Interleukins
Kaempferol
Lipids
Liquid chromatography
Male
Myocardium
Oral administration
Oxidative stress
Phenols
Propanolol hydrochloride
Propranolol
Quercetin
Rats
Research Article
Rutin
Scavenging
Seaweed
Seaweeds
Serum levels
Signal transduction
Thyroid
Thyroid gland
Thyroxine
Triglycerides
Ulva
Ulva fasciata
Waste Water Technology
Water Management
Water Pollution Control
title The possible role of the seaweed Ulva fasciata on ameliorating hyperthyroidism-associated heart inflammations in a rat model
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