Spinal morphine administration reduces the fatty acid contents in spinal cord and brain by increasing oxidative stress

• Published in: Neurochemical research Vol. 32; no. 1; pp. 19 - 25
• Main Authors: Ozmen, Ismail, Naziroğlu, Mustafa, Alici, H Ahmet, Sahin, Fikrettin, Cengiz, Mustafa, Eren, Ibrahim
• Format: Journal Article
• Language: English
• Published: United States Springer Nature B.V 01.01.2007
• Subjects: Animals; Brain Chemistry - drug effects; Fatty Acids - metabolism; Glutathione - metabolism; Injections, Spinal; Lipid Peroxidation - drug effects; Male; Morphine - administration & dosage; Morphine - pharmacology; Oxidative Stress - drug effects; Rabbits; Random Allocation; Spinal Cord - chemistry; Spinal Cord - metabolism
• ISSN: 0364-3190; 1573-6903
• DOI: 10.1007/s11064-006-9217-5

It is well known that oxidative stress damages biomolecules such as DNA and lipids. No study is available on the morphine-induced oxidative damage and fatty acids changes in brain and spinal tissues. The aim of this work was to determine the effects of morphine on the concentrations and compositions of fatty acid in spinal cord segments and brain tissues in rabbits as well as lipid peroxidation (LP) and glutathione (GSH) levels in cortex brain. Twelve New Zealand albino rabbits were used and they were randomly assigned to two groups of 6 rabbits each. First group used as control although morphine administrated to rats in second group. Cortex brain and (cervical, thoracic, lumbar) samples were taken. The fatty acids between n:18.0 and 21.0 were present in spinal cord sections and n:10 fatty acids in control animals were present in the brain tissues. Compared to n:20.0-24.0 fatty acids in spinal cord sections and 8.0 fatty acids in the brain tissues of drug administered animals. The concentration and composition of the fatty acid methyl esters in spinal cord and brain tissues was decreased by morphine treatments. LP levels in the cortex brain were increased although GSH levels were decreased by the morphine administration. In conclusion, unsaturated fatty acids contents in brain and spinal cord sections and GSH were reduced by administrating spinal morphine although oxidative stress as LP increased. The inhibition oxidative damage may be a useful strategy for the development of a new protection for morphine administration as well as opiate abuse.