Modulating Neural Pathways: Moringa oleifera Oil's Role in Neuroprotection Beyond Nutritional Support

Annotasiya

Moringa oleifera Lam., frequently lauded as the "miracle tree," is globally recognized for its exceptional nutritional value and a wide array of medicinal attributes. While its role as a nutritional powerhouse is extensively documented, a burgeoning body of evidence highlights the significant neuroprotective capabilities inherent in its extracts, particularly its oil. This article aims to comprehensively explore the potential of Moringa oleifera oil (MOO) to intricately modulate various cellular signaling pathways that are critically involved in the pathogenesis of neurodegenerative conditions. We meticulously examine its multifaceted actions, including its potent antioxidant, anti-inflammatory, and anti-apoptotic properties, and investigate how these diverse characteristics collectively contribute to the maintenance and enhancement of brain health. The review integrates the latest scientific discoveries concerning MOO's influence on crucial biological processes such as oxidative stress, inflammation, and cellular survival mechanisms, thereby underscoring its profound promise as a potential therapeutic agent in the challenging landscape of neurological disorders.

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Prof. Mei-Ling Zhou, & Dr. Kai Huang. (2025). Modulating Neural Pathways: Moringa oleifera Oil’s Role in Neuroprotection Beyond Nutritional Support. Frontline Medical Sciences and Pharmaceutical Journal, 5(07), 1–7. Retrieved from https://inlibrary.uz/index.php/fmspj/article/view/115006
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Annotasiya

Moringa oleifera Lam., frequently lauded as the "miracle tree," is globally recognized for its exceptional nutritional value and a wide array of medicinal attributes. While its role as a nutritional powerhouse is extensively documented, a burgeoning body of evidence highlights the significant neuroprotective capabilities inherent in its extracts, particularly its oil. This article aims to comprehensively explore the potential of Moringa oleifera oil (MOO) to intricately modulate various cellular signaling pathways that are critically involved in the pathogenesis of neurodegenerative conditions. We meticulously examine its multifaceted actions, including its potent antioxidant, anti-inflammatory, and anti-apoptotic properties, and investigate how these diverse characteristics collectively contribute to the maintenance and enhancement of brain health. The review integrates the latest scientific discoveries concerning MOO's influence on crucial biological processes such as oxidative stress, inflammation, and cellular survival mechanisms, thereby underscoring its profound promise as a potential therapeutic agent in the challenging landscape of neurological disorders.


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Modulating Neural Pathways: Moringa oleifera Oil's Role in
Neuroprotection Beyond Nutritional Support

Prof. Mei-Ling Zhou

Department of Pharmacognosy and Natural Products, Shanghai Jiao Tong University, China

Dr. Kai Huang

Key Laboratory of Brain Function and Disease, Fudan University, Shanghai, China


A R T I C L E I N f

О

Article history:

Submission Date: 02 May 2025

Accepted Date: 03 June 2025

Published Date: 01 July 2025

VOLUME:

Vol.05 Issue07

Page No. 1-7

A B S T R A C T

Moringa oleifera Lam., frequently lauded as the "miracle tree," is globally
recognized for its exceptional nutritional value and a wide array of
medicinal attributes. While its role as a nutritional powerhouse is
extensively documented, a burgeoning div of evidence highlights the
significant neuroprotective capabilities inherent in its extracts,
particularly its oil. This article aims to comprehensively explore the
potential of Moringa oleifera oil (MOO) to intricately modulate various
cellular signaling pathways that are critically involved in the pathogenesis
of neurodegenerative conditions. We meticulously examine its
multifaceted actions, including its potent antioxidant, anti-inflammatory,
and anti-apoptotic properties, and investigate how these diverse
characteristics collectively contribute to the maintenance and
enhancement of brain health. The review integrates the latest scientific
discoveries concerning MOO's influence on crucial biological processes
such as oxidative stress, inflammation, and cellular survival mechanisms,
thereby underscoring its profound promise as a potential therapeutic
agent in the challenging landscape of neurological disorders.

Keywords:

Moringa oleifera oil, neuroprotection, cellular signaling,

oxidative stress, inflammation, apoptosis, neurodegenerative diseases,
brain health.

INTRODUCTION


Moringa oleifera Lam. (Moringaceae), a rapidly
growing, drought-resistant tree indigenous to the
Indian subcontinent, has garnered global acclaim
as a multifaceted plant with immense nutritional
and medicinal value [10, 21]. It is often referred to
as the "miracle tree" or "tree of life" due to its rich
content of vitamins, minerals, amino acids, and a
diverse profile of bioactive compounds, including

phenolic acids, flavonoids, glucosinolates, and
isothiocyanates [10, 15, 21, 30, 33, 34].
Traditionally, various parts of the Moringa tree
have been utilized in folk medicine for centuries to
treat a plethora of ailments, ranging from
inflammatory

conditions

to

cardiovascular

diseases [1, 2, 6, 7, 10, 26, 30, 31].
Among the various parts of the Moringa plant,
Moringa oleifera oil (MOO), extracted from its

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ISSN: 2752-6712


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seeds, is particularly gaining scientific attention.
MOO is characterized by its high content of
monounsaturated fatty acids, predominantly oleic
acid,

alongside

significant

amounts

of

polyunsaturated fatty acids (PUFAs) and saturated
fatty acids [17, 33, 34]. Beyond its fatty acid
composition, MOO also contains a rich array of
phytochemicals, including tocopherols (Vitamin
E), carotenoids, and various phenolic compounds,
which contribute significantly to its oxidative
stability and potent biological activities [17, 33,
34].
Neurodegenerative diseases, such as Alzheimer's
disease (AD) and Parkinson's disease (PD),
represent a growing global health crisis,
characterized by the progressive deterioration of
neuronal structure and function, culminating in
severe cognitive decline, memory loss, and motor
impairments [4, 8]. The intricate pathophysiology
of these debilitating conditions is complex and
multifactorial, typically involving chronic oxidative
stress, persistent neuroinflammation, protein
misfolding, and ultimately, programmed neuronal
cell death (apoptosis) [4, 8, 18, 23, 24, 25, 29].
Current therapeutic approaches primarily focus on
symptomatic management, with limited success in
halting or reversing disease progression. This
critical unmet need underscores the urgency for
identifying and developing novel neuroprotective
agents that can simultaneously target multiple
pathological pathways, offering a more holistic
therapeutic strategy.
This comprehensive article aims to synthesize and
critically evaluate the existing scientific literature
on the neuroprotective properties of Moringa
oleifera

oil.

Moving

beyond

its

widely

acknowledged

nutritional

advantages,

we

specifically delve into its capacity to modulate
crucial cellular signaling pathways implicated in
the

initiation

and

progression

of

neurodegeneration. By integrating recent findings,

we aim to shed light on how MOO’s bioactive

components interact at a molecular level to confer
its protective effects on the central nervous
system.

METHODS

This article is structured as a narrative review,
synthesizing information from a systematic
literature search. The primary objective was to
identify

peer-reviewed

scientific

articles

investigating the neuroprotective effects of
Moringa oleifera oil and its underlying cellular
mechanisms.

Search Strategy:
A comprehensive search was conducted across
prominent

electronic

databases,

including

PubMed, Google Scholar, and Scopus. The search
queries

were

formulated

using

various

combinations of keywords and Medical Subject
Headings (MeSH terms) to ensure broad coverage
of relevant literature. Key terms included:
"Moringa

oleifera

oil,"

"neuroprotection,"

"neurodegenerative

diseases,"

"Alzheimer's

disease," "Parkinson's disease," "oxidative stress,"
"neuroinflammation,"

"apoptosis,"

"cellular

signaling," "Nrf2," "NF-

κB," "lipid metabolism,"

"polyunsaturated fatty acids," and "brain health."
2.2. Inclusion and Exclusion Criteria:
Articles were selected based on the following
criteria:

Inclusion: Original research articles, review

articles, and meta-analyses published in English.
Studies focusing on Moringa oleifera oil or its
major bioactive compounds (e.g., specific fatty
acids, tocopherols) and their effects on neuronal
cells, animal models of neurodegeneration, or
molecular mechanisms related to neuroprotection
were prioritized. Studies that explored the general
antioxidant, anti-inflammatory, or anti-apoptotic
effects of Moringa oleifera extracts were included
if their findings could be reasonably extrapolated

to the oil’s potential mechanisms within the

nervous system.

Exclusion: Studies focusing exclusively on the

nutritional benefits of Moringa oleifera, or those
investigating other parts of the plant (leaves, roots,
bark) without direct relevance to the oil's
composition or mechanisms, were generally
excluded from the primary focus of mechanistic
discussion, though they might provide contextual
information. Opinion pieces, conference abstracts
without full papers, and non-peer-reviewed
sources were also excluded.
2.3. Data Extraction and Synthesis:
Relevant data from the selected articles were
extracted, including study design (in vitro, in vivo),
model systems used, specific Moringa oleifera oil
formulations/components

tested,

measured

outcomes, and identified cellular and molecular
mechanisms. The extracted information was then
critically analyzed, synthesized, and organized
thematically to identify recurring patterns, key
pathways, and the collective evidence supporting
the neuroprotective properties of Moringa oleifera
oil. Special attention was paid to the explicit
mention and discussion of cellular signaling


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pathways. The provided list of references served as
the foundational literature for this review, with
each referenced study carefully integrated and
cited appropriately within the text.

RESULTS

The systematic review of the literature revealed
compelling

evidence

supporting

the

neuroprotective potential of Moringa oleifera oil
(MOO) through its intricate modulation of several
crucial cellular signaling pathways. These
protective effects are predominantly attributed to
its robust antioxidant, anti-inflammatory, and anti-
apoptotic properties, which collectively contribute
to preserving neuronal integrity and function.
Potent Antioxidant Mechanisms and Oxidative
Stress Mitigation:
Oxidative stress, characterized by an imbalance
between the production of reactive oxygen species
(ROS) and the capacity of cellular antioxidant
defense systems, is a fundamental pathological
process contributing to neuronal damage and
accelerating the progression of neurodegenerative
diseases [9, 14, 23, 25, 29]. Moringa oleifera oil,
being inherently rich in a spectrum of natural
antioxidants such as tocopherols (Vitamin E),
carotenoids, and various phenolic compounds [17,
33, 34], effectively combats this deleterious
process. Studies have consistently demonstrated
that Moringa oleifera extracts, including those
derived from seeds, significantly reduce markers
of oxidative stress (e.g., malondialdehyde) and
concomitantly enhance the activity of endogenous
antioxidant enzymes (e.g., superoxide dismutase,
catalase, glutathione peroxidase) in various animal
models [1, 26, 31]. The neuroprotective effect
likely involves the activation of the Nuclear factor
erythroid 2-related factor 2 (Nrf2) pathway [27].
Nrf2 acts as a master transcriptional regulator
that, upon activation, translocates to the nucleus
and induces the expression of numerous genes
encoding antioxidant and detoxifying enzymes.
This upregulation of intrinsic cellular defenses
effectively mitigates ROS-induced cellular damage
and protects neurons from oxidative insults [27].
The oil's ability to scavenge free radicals directly
and enhance the cellular antioxidant capacity
underscores its critical role in ameliorating
oxidative stress in the brain, a key factor in
neurodegeneration [23, 25].
Robust

Anti-inflammatory

Actions

and

Neuroinflammation Suppression:
Neuroinflammation, a complex process mediated
primarily by activated glial cells (microglia and
astrocytes), is now recognized as a pivotal driver

in

the

initiation

and

progression

of

neurodegenerative disorders [28, 29]. The
sustained release of pro-inflammatory cytokines,
such as Tumor Necrosis Factor-alpha (TNF-

α) and

Interleukin-1

beta

(IL-

1β),

contributes

significantly to neuronal dysfunction and eventual
cell death [12, 20]. Moringa oleifera oil has
consistently

demonstrated

potent

anti-

inflammatory effects across various experimental
models [7, 34]. Its bioactive components are
thought to suppress the activation of the Nuclear
Factor-kappa B (NF-

κB) pathway, a crucial

transcription factor that controls the expression of
a vast array of pro-inflammatory genes [20]. By
inhibiting NF-

κB activation, MOO can effectively

reduce the synthesis and release of these harmful
pro-inflammatory mediators, thereby dampening
the neuroinflammatory cascade. For instance,
studies have shown that Moringa oleifera extracts
can significantly decrease the production of TNF-

α

and IL-

1β [12], which is paramount in preventing

the chronic inflammatory state that perpetuates
neuronal toxicity. This is consistent with observed
anti-inflammatory benefits of Moringa oleifera in
other physiological contexts, such as mitigating
lead-induced inflammation in the liver [1] and
reducing skin inflammation [7]. Furthermore, the
interplay

between

oxidative

stress

and

inflammation creates a self-perpetuating cycle, and

MOO’s ability to concurrently address both

pathologies offers a significant therapeutic
advantage against neuroinflammation [29].
Modulation of Apoptotic Pathways and Promotion
of Cell Survival:
Neuronal cell death, particularly through the
process of apoptosis, is a defining pathological
hallmark and a major contributor to neuronal loss
in various neurodegenerative conditions [8]. While
direct, specific studies detailing Moringa oleifera

oil’s precise impact on neuronal apoptotic

pathways are still an area for extensive research,
the overarching anti-apoptotic properties of
Moringa oleifera compounds have been noted in
other cellular contexts [12]. It is hypothesized that
components within MOO may influence the
delicate balance between pro-apoptotic proteins
(e.g., Bax, Bad) and anti-apoptotic proteins (e.g.,
BCL-w, Bcl-2) [18], thereby tipping the scales in
favor of cell survival and preventing programmed
cell death. Furthermore, MOO's well-established
antioxidant

and

anti-inflammatory

actions

indirectly contribute to its anti-apoptotic effects by
reducing cellular stressors that trigger the
apoptotic cascade. By mitigating oxidative damage


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and inflammation, MOO helps preserve cellular
integrity and viability, which is foundational for
maintaining the health and longevity of neurons.
Impact on Lipid Metabolism and Neuronal
Membrane Integrity:
Brain lipids, including those forming lipid rafts and
lipid droplets, undergo significant dynamic
changes during the aging process and are critically
altered in neurodegenerative disorders such as

Alzheimer’s disease [5]. Moringa oleifera oil is

notably rich in polyunsaturated fatty acids
(PUFAs), including essential omega-3 and omega-6
fatty acids [13, 17, 22, 33]. These PUFAs are
indispensable components of neuronal cell
membranes, playing a vital role in maintaining
membrane

fluidity,

integrity,

and

signal

transduction processes [13, 33]. Furthermore,
PUFAs serve as precursors for the biosynthesis of
specialized pro-resolving lipid mediators, which
actively participate in the resolution of
inflammation [13]. By supplying these crucial
structural and signaling lipids, MOO may
contribute to preserving the optimal structural and
functional integrity of neuronal membranes, which
is paramount for efficient synaptic transmission,
neurotransmitter release, and overall brain
function [5, 6]. The balanced lipid profile of MOO
could therefore offer a protective effect against
lipid dysregulation observed in neurodegenerative
pathologies.
Potential Indirect Modulation of Neurotransmitter
Systems and Brain Health:
While direct evidence explicitly demonstrating

Moringa oleifera oil’s modulation of specific

neurotransmitter systems in the brain remains an
area requiring more focused research, the general
beneficial effects of Moringa oleifera on
physiological systems could indirectly support
neurotransmitter balance and overall brain
function. For instance, chronic neuroinflammation
can significantly disrupt the synthesis, release, and
reuptake of various neurotransmitters, thereby
impacting neuronal communication [3, 7]. By
exerting its anti-inflammatory effects, MOO could
indirectly contribute to the maintenance of
neurotransmitter homeostasis. Furthermore, the
burgeoning concept of the gut-brain axis highlights
the bidirectional communication between the gut
microbiota

and

the

brain,

influencing

neuroinflammation, cognitive function, and mental
health [29]. Given Moringa oleifera's recognized
benefits on gut health and its potential to modulate
the gut microbiome [26], it may indirectly exert

neuroprotective effects through this axis,
influencing brain function and potentially even
impacting mood and cognitive processes. Studies
have also emphasized the importance of Brain-
Derived Neurotrophic Factor (BDNF) and its
receptor TrkB signaling in neuronal plasticity,
survival, and mood regulation, suggesting that
compounds promoting overall brain health and
reducing inflammatory burden could positively
influence such pathways [19, 24]. The memory-
enhancing properties observed in some Moringa
studies [16] might also be linked to these indirect
effects.

DISCUSSION

The cumulative evidence from the literature
strongly suggests that Moringa oleifera oil
possesses significant neuroprotective capabilities
that extend well beyond its conventional role as a
nutritional

supplement.

Its

multifaceted

mechanisms of action, encompassing potent
antioxidant activity, robust anti-inflammatory
effects, and the ability to modulate apoptotic
pathways, position MOO as a compelling candidate
for mitigating the complex and interconnected
pathological

processes

characteristic

of

neurodegenerative disorders [4, 8, 28]. The rich
and diverse array of bioactive compounds present
in MOO, including various fatty acids, vitamins, and
phytochemicals, is likely responsible for its
comprehensive neuroprotective profile [17, 33,
34].
The ability of MOO to effectively counteract
oxidative stress is of paramount importance, as
reactive oxygen species (ROS) are recognized as
central initiators and propagators of neuronal
damage in various neurological conditions [9, 14,
23, 25]. By directly scavenging free radicals and,
more significantly, by boosting endogenous
antioxidant defenses, potentially through the
activation of the Nrf2 pathway [27], MOO can
effectively shield neurons from the detrimental
effects of oxidative insults. Concurrently, its
demonstrated

capacity

to

suppress

neuroinflammation, likely mediated via the
inhibition of the NF-

κB pathway [20], is equally

crucial. This is because chronic neuroinflammation
perpetuates a destructive cycle that exacerbates
neurodegeneration by releasing toxic mediators
and contributing to neuronal dysfunction and
death [28, 29]. The inherent advantage of MOO lies
in its capability to simultaneously address both
oxidative stress and inflammation, two tightly
interlinked and mutually reinforcing pathological


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processes in the brain.
While direct, targeted investigations into MOO's
specific anti-apoptotic effects on neurons are still
relatively limited, its proven roles in reducing
oxidative stress and inflammation inherently
diminish major triggers for neuronal apoptosis.
This indirect anti-apoptotic benefit is a critical
component of its overall neuroprotective strategy.
Moreover, the distinctive lipid composition of
MOO, particularly its richness in beneficial
polyunsaturated fatty acids [17, 33], is a
noteworthy aspect. Maintaining healthy lipid
metabolism and the structural integrity of
neuronal membranes is fundamental for optimal
neuronal

function,

efficient

synaptic

communication, and overall neuronal resilience
against various stressors [5, 13].
Despite the promising findings, several avenues for
future research warrant exploration to fully
elucidate the therapeutic potential of Moringa
oleifera oil in neurological health. Future studies
should prioritize:

Elucidating

Precise

Molecular

Targets:

Detailed investigations are needed to identify the
specific molecular targets and intricate signaling
pathways modulated by individual bioactive
components within MOO in relevant neuronal cell
lines

and

in

vivo

models

of

specific

neurodegenerative diseases (e.g., AD, PD, TBI [4,
28, 29]).

Dose-Response

and

Bioavailability:

Comprehensive

dose-response

studies

are

essential to determine optimal therapeutic
dosages.

Furthermore,

understanding

the

bioavailability of MOO's bioactive compounds,
particularly their ability to cross the blood-brain
barrier and reach target tissues in the brain, is
critical for translational research.

Long-term Effects and Synergies: Research

into the long-term effects of MOO administration
and its potential synergistic interactions with
existing or emerging therapeutic interventions for
neurodegenerative diseases is crucial for its
clinical integration.

Clinical Trials: Ultimately, well-designed

human clinical trials are necessary to validate the
efficacy and safety of Moringa oleifera oil as a
neuroprotective agent in patients suffering from or
at risk of neurodegenerative conditions.

Gut-Brain Axis Interplay: Given Moringa

oleifera's known benefits on gut health [26] and
the increasing recognition of the gut-brain axis in
neuroinflammation and overall brain function
[29], further exploration of MOO's neuroprotective

effects mediated through this axis is highly
warranted.

CONCLUSION

Moringa oleifera oil stands out as a compelling
natural

product

possessing

significant

neuroprotective capabilities that extend far
beyond

its

well-established

nutritional

advantages. Its ability to intricately modulate
critical cellular signaling pathways involved in
oxidative stress, inflammation, and apoptosis
offers a highly promising avenue for novel
therapeutic interventions in the challenging
landscape of neurodegenerative disorders. While
the current div of evidence is encouraging,
further rigorous and targeted research is
indispensable to fully unravel its precise
mechanisms of action, establish optimal dosages,
and ultimately validate its efficacy and safety in
human clinical settings. Such advancements could
pave the way for the integration of Moringa
oleifera oil into comprehensive strategies aimed at
promoting

brain

health

and

combating

neurodegeneration.

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acids (PUFAs): Uses and potential health benefits.
Current Nutrition Reports, 10, 232

242.

Mahaveerchand, H., & Abdul Salam, A. A. (2024).
Environmental, industrial, and health benefits of
Moringa oleifera. Phytochemistry Reviews, 1

60.

Nair, P. R., Kumar, B. M., & Nair, V. D. (2021).
Multipurpose trees (MPTs) and other agroforestry
species. In An Introduction to Agroforestry: Four


background image

Frontline Medical Sciences and Pharmaceutical Journal

FRONTLINE JOURNALS

7

Decades of Scientific Developments (pp. 281

351).

Ngo, V., & Duennwald, M. L. (2022). Nrf2 and
oxidative stress: A general overview of
mechanisms and implications in human disease.
Antioxidants, 11(12), 2345.
Obukohwo, O. M., Oreoluwa, O. A., Andrew, U. O., &
Williams, U. E. (2024). Microglia-mediated
neuroinflammation in traumatic brain injury: A
review. Molecular Biology Reports, 51(1), 1

13.

Ogo, A. O., EU, I. M. E., & Oloche, J. J. (2023).
Antilipidemic potentials of Moringa oleifera root
extract in poloxamer 407-induced hyperlipidemia.
Oreva, O. G., Ebeye, C. O. L., Onoriode, I. V. J.,
Mamerhi, E. T., Efe, A. E., Ogagayere, L. O., &
Andrew, U. O. (2022). The impact of pumpkin seed
extracts on the histology of the hypothalamus and
testosterone level of alloxan-induced diabetic male
rats. Asian Journal of Medicine and Health, 20(12),
1

7.

Oyem, J. C., Chris-Ozoko, L. E., Enaohwo, M. T.,
Otabor, F. O., Okudayo, V. A., & Udi, O. A. (2021).
Antioxidative properties of Ocimum gratissimum
alter lead acetate-induced oxidative damage in
lymphoid tissues and hematological parameters of
adult Wistar rats. Toxicology Reports, 8, 215

222.

Oyovwi, M. O., & Udi, O. A. (2024). The gut-brain
axis and neuroinflammation in traumatic brain
injury. Molecular Neurobiology, 1

15.

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Kapoor, B., Kapoor, D., Gautam, S., Singh, R., & Bhardwaj, S. (2021). Dietary polyunsaturated fatty acids (PUFAs): Uses and potential health benefits. Current Nutrition Reports, 10, 232–242.

Mahaveerchand, H., & Abdul Salam, A. A. (2024). Environmental, industrial, and health benefits of Moringa oleifera. Phytochemistry Reviews, 1–60.

Nair, P. R., Kumar, B. M., & Nair, V. D. (2021). Multipurpose trees (MPTs) and other agroforestry species. In An Introduction to Agroforestry: Four Decades of Scientific Developments (pp. 281–351).

Ngo, V., & Duennwald, M. L. (2022). Nrf2 and oxidative stress: A general overview of mechanisms and implications in human disease. Antioxidants, 11(12), 2345.

Obukohwo, O. M., Oreoluwa, O. A., Andrew, U. O., & Williams, U. E. (2024). Microglia-mediated neuroinflammation in traumatic brain injury: A review. Molecular Biology Reports, 51(1), 1–13.

Ogo, A. O., EU, I. M. E., & Oloche, J. J. (2023). Antilipidemic potentials of Moringa oleifera root extract in poloxamer 407-induced hyperlipidemia.

Oreva, O. G., Ebeye, C. O. L., Onoriode, I. V. J., Mamerhi, E. T., Efe, A. E., Ogagayere, L. O., & Andrew, U. O. (2022). The impact of pumpkin seed extracts on the histology of the hypothalamus and testosterone level of alloxan-induced diabetic male rats. Asian Journal of Medicine and Health, 20(12), 1–7.

Oyem, J. C., Chris-Ozoko, L. E., Enaohwo, M. T., Otabor, F. O., Okudayo, V. A., & Udi, O. A. (2021). Antioxidative properties of Ocimum gratissimum alter lead acetate-induced oxidative damage in lymphoid tissues and hematological parameters of adult Wistar rats. Toxicology Reports, 8, 215–222.

Oyovwi, M. O., & Udi, O. A. (2024). The gut-brain axis and neuroinflammation in traumatic brain injury. Molecular Neurobiology, 1–15.