Neurodegeneration
is one of the most common diseases in the aged population, characterized
by the loss in the function of neuronal cells and their ultimate death.
One of the common features in the progression of this type of diseases
is the oxidative stress. Drugs which are currently being used have
been found to show lateral side effects, which is partly due to their
inefficiency to cross blood–brain barrier. Nanoencapsulation
of bioactive compounds is a profound approach in this direction and
has become a method of choice nowadays. This study involved the evaluation
of the anti-oxidative properties of magnoflorine (MF), which is an
aporphine quaternary alkaloid, and synthesis of MF-loaded chitosan–collagen
nanocapsules (MF-CCNc) for its better efficacy as a potent anti-oxidant.
Physiochemical characterization of the synthesized nanocapsules was
done by using dynamic light scattering and transmission electron microscopy.
It revealed that the synthesized nanocapsules are of small size range,
as small as 12 ± 2 nm, and are more or less of spherical shape.
Sustained release was shown by MF in the
in vitro
drug release studies. Both MF and MF-CCNc were found to have good
anti-oxidant potential with IC
50
< 25 μg/mL. No
major cytotoxicity was shown by the synthesized nanocapsules on SH-SY5Y
cells.
In silico
anti-acetylcholinesterase (AChE)
studies were also done, and they revealed that MF can be a potent
inhibitor of AChE.
Dementia or the loss of cognitive functioning is one of the major health issues in elderly people. Alzheimer's disease (AD) is one of the common forms of dementia. Treatment chiefly involves the use of acetylcholinesterase (AChE) inhibitors in AD. However, oxidative stress has also been found to be involved in the proliferation of the disease. Magnoflorine is one of the active compounds of Coptidis Rhizoma and has high anti-oxidative properties. Active principle-loaded nanoparticles have shown increased efficiency for neurodegenerative diseases due to their ability to cross the blood−brain barrier more easily. An in vitro study involving magnoflorine-loaded chitosan collagen nanocapsules (MF-CCNc) has shown them to possess inhibitory effects against oxidative stress and to some extent on AChE as well. In the current study, both nootropic and anti-amnesic effects of magnoflorine and MF-CCNc on scopolamine-induced amnesia in rats were evaluated. The treatment was done intraperitoneally (i.p.) once daily for 17 consecutive days with MF-CCNc (0.25, 0.5, and 1 mg), magnoflorine (1 mg), and donepezil (1 mg). To induce amnesia, hence, cognitive deficit rats were induced with scopolamine (1 mg/kg) daily for the last 9 days. Novel object recognition (NOR) and elevated plus maze (EPM) behavioral analysis were done to assess memory functioning. Hippocampal tissues were extracted to study the effect on biochemicals (AChE, MDA, SOD, and CAT), pro-inflammatory cytokines (IL-1β, IL-6, and TNF-α), and immunohistochemistry (brain-derived neurotrophic factor (BDNF) and DCX). MF-CCNc showed memory-enhancing effects in nootropic as well as chronic scopolamine-treated rats in NOR and an increase in inflexion ratio in EPM. MF-CCNc reduced the levels of AChE and MDA while increasing SOD and CAT levels in the hippocampus. MF-CCNc further lowered the levels of proinflammatory cytokines IL-1β, IL-6, and TNF-α. These nanocapsules further increased the expression of BDNF and DCX that are necessary for adult neurogenesis. From the research findings, it can be concluded that MF-CCNc has high anti-amnesic properties and could be a promising candidate for the treatment of AD.
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