Researchers at UNC School of Medicine have discovered a potential environmental cause of autism - prescription drugs that interfere with a critical process in DNA called topoisomerases. Ordinarily, DNA is wound tightly in packages to ensure efficient storage and must be unwound during cell division and gene expression. Topoisomerases make the unwinding possible that is necessary during these two crucial processes.
Professors Mark Zylka and Benjamin Philpot made the discovery while studying a drug that’s effective against cancer and discovered that this cancer drug impacted topoisomerases. Tompoisonmerases regulate really long genes and the genes identified as being associated with autism are really long. This led the professors to the insight that inhibiting topoisomerases might increase the risk of autism. In addition, most of the affected genes related to brain development in utero as well as early childhood meaning exposure to certain pharmaceuticals during those critical time periods could lead to lifelong effects such as autism even after the exposure ended.
The researchers were studying a chemo drug called topotecan but point out that other drugs such as antibiotics and antifungals also inhibit topoisomerase enzymes and this could lead to autism. The antibiotics that inhibit antibiotics are known Quinolone antibiotics. They go by the following
Flumequine Nalidixic acid Enoxacin
Oxolinic acid Piromidic acid Lomefloxacin
Pipemidic acid Rosoxacin Nadifloxacin
Ciprofloxacin Ofloxacin Pefloxacin
Norfloxacin Balofloxacin Gatifloxacin
Rufloxacin Grepafloxacin Levofloxacin
Moxifloxacin Pazufloxacin Sparfloxacin
Temafloxacin Tosufloxacin Clinafloxacin
Gemifloxacin Sitafloxacin Trovafloxacin
Prulifloxacin
Antifungals such as fluconazole have also been shown to inhibit topoisomerase.