Assessment of Biochemical Determinants in Multiple Sclerosis Patients Following the Oral Administration of β-D-Mannuronic Acid (M2000)

Curr Drug Discov Technol. 2021;18(5):e17092020186049. doi: 10.2174/1570163817999200918104333.

Abstract

Background: Multiple sclerosis is an autoimmune chronic inflammatory disease of the central nervous system that can lead to some serious disabilities. Despite using various immunomodulatory and anti-inflammatory drugs that have therapeutic effects, they cannot reduce its progression completely and have some unwanted side effects too. The immunomodulatory and anti-inflammatory effects of the β-D-Mannuronic acid (M2000) have been proven in several surveys, and the present research was designed to determine its toxicity and therapeutic effects in MS patients.

Methods: This study was performed on 15 MS patients who took 25 mg/kg/day the oral form of the β-D-Mannuronic acid for six months, and 15 healthy people as a control group. Serum levels of Urea, Creatinine, GGT, Vitamin D3, Uric acid, and Anti-Phospholipids were compared to evaluate the therapeutic and possible toxic effects of this drug after this period.

Results: Non- toxic effects through the study of urea, creatinine, GGT, and non-significant changes in uric acid and anti-Phospholipids levels, besides a significant rise in vitamin, D3 levels in the M2000 treated cases were found.

Conclusions: Our results suggested that β-D-Mannuronic acid is a safe drug and has no toxicity when administered orally and also has some therapeutic effects in MS patients.

Keywords: M2000; Mannuronic acid; NSAIDs.; biochemical markers; drug safety; multiple sclerosis; toxicology.

MeSH terms

  • Administration, Oral
  • Anti-Inflammatory Agents, Non-Steroidal / therapeutic use
  • Hexuronic Acids
  • Humans
  • Multiple Sclerosis* / drug therapy

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Hexuronic Acids
  • mannuronic acid

Associated data

  • IRCT/IRCT2017042313739N6