Stabilization of mitochondrial and microsomal function by polysaccharide of Ulva lactuca on d-galactosamine induced hepatitis in rats
Abstract
In this study we used liver mitochondrial and microsomal fraction from rats pretreated with seaweed Ulva lactuca polysaccharide extract (ULP - 200mg/kg body weight, daily for 21 days, oral gavage) on D-Galactosamine (500mg/kg body weight, intraperitoneally) challenge. Effectiveness of ULP was determined based on functional status of trichloro acetic acid (TCA), urea cycle, and microsomal enzymes. The composition of sulfate polysaccharide content such as total sugars, sulfate and uronic acid were examined. In addition the fine ultra structural changes were examined using electron microscopy (EM). We observed significant (p<0.001) mitochondrial and microsomal abnormalities during liver damage by D-Galactosamine, consequently altering enzymes of energy metabolism. Electron microscopy of D-Galactosamine intoxicated rat liver tissue revealed the swelling and loss of mitochondrial cristae. Conversely the rats pretreated with ULP against D-Galactosamine challenge prevented (p<0.05) the significant abnormality of TCA, microsomal enzymes and severity of mitochondria as observed in EM study in rats injected with D-Galactosamine alone. However no effective prevention was observed in urea cycle enzymes among D-Galactosamine and treatment group rats. These results showed the effectiveness of ULP in stabilizing the functional status of mitochondrial and microsomal membrane which might be due to the presence of sulfated polysaccharide that could prevented the oxidative stress induced by D-Galactosamine intoxication.
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There are several reports concerning antioxidant activities of ulvans in experimental D-galactosamine-induced hepatitis in rats.
“There are several reports concerning the antioxidant activities of ulvans in experimental D-galactosamine-induced hepatitis in rats [112,113].”
From Anticancer and Cancer Preventive Properties of Marine Polysaccharides: Some Results and Prospects (2013) · cites this paper as [112]
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References 40 · Cited by 48
- Authors
- Devaki, T., Sathivel, A., & BalajiRaghavendran, H. R.
- Affiliations
- University of Madras (IN)
- Saveetha University (IN)
- Venue
- Chemico-Biological Interactions
- Publisher
- Elsevier BV
- Published
- 2009-01
- Volume
- 177
- Issue
- 2
- Pages
- 83-88
- ISSN
- 0009-2797 (ISSN-L)
- OpenAlex
- W2073328758
- Cited by
- 48
- References
- 40
- Citations by year
- 2026: 1 · 2025: 1 · 2024: 3 · 2023: 2 · 2022: 2 · 2021: 5 · 2020: 1 · 2019: 5 · 2018: 1 · 2017: 4 · 2016: 5 · 2015: 4 · 2014: 2 · 2013: 4 · 2012: 3
- FWCI
- 2.52
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Chemico-Biological Interactions (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Agricultural and Biological Sciences › Aquatic Science › Seaweed-derived Bioactive Compounds
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmacology › Drug-Induced Hepatotoxicity and Protection
- Health Sciences › Medicine › Complementary and alternative medicine › Medicinal plant effects and applications
- Keywords
- Ulva lactuca, seaweed polysaccharides, microsomal enzymes, TCA cycle, urea cycle, oxidative stress, sulfated polysaccharides, hepatoprotection, liver ultrastructure
- MeSH terms
- Administration, Oral, Animals, Disease Models, Animal, Galactosamine, Injections, Intraperitoneal, Male, Microsomes, Liver, Mitochondria, Liver, Plant Extracts, Polysaccharides, Trichloroacetic Acid, Urea, Rats, Wistar, Hepatocytes, Ulva, Mitochondrial Membranes, Rats, Chemical and Drug Induced Liver Injury
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