Results from the study reveal that injected paclitaxel appear to restore nerve function in an animal model. In the study, it was demonstrated that low and medium doses of Pacxeed had two major effects, namely improving axonal transport and increasing the amounts of tubulin and microtubules, proteins and cell structures vital for nerve structure and conduction.
Abnormal tau proteins are often seen as mechanisms that can lead to brain degeneration in Alzheimer’s disease and other neurodegenerative disorders known as taupathies. In all taupathies, there are neuropathologic aggregates of paired helical filaments and/or straight filaments composed of aberrantly phosphorylated tau proteins in central nervous system neurons or glia.
It has been shown that these abnormally filamentous proteins cannot perform the important functions of binding and stabilizing microtubules which often leads to a dramatic increase in neurofibrillary tangles and neuropil threads seen in Alzheimer’s.
Angiotech, which markets Paxceed, believes that systemic paclitaxel, a microtubule-stabilizing agent, may ultimately show a therapeutic benefit to patients with Alzheimer’s disease and other taupathies by offsetting the loss of normal tau function.
“We are excited as this is the first experimental evidence to support the use of paclitaxel as a novel intervention for the treatment of Alzheimer’s and other neurodegenerative diseases,” said Dr William Hunter, CEO of Angiotech. “We have long believed that a microtubule-stabilizing agent used systemically would hold great promise in these types of diseases, and we look forward to advancing the results of these studies into humans.”