REM Sleep Deprivation, Pain, Oxidative Stress, and Tualang Honey

| Posted in: Science

Journal name: The Malaysian Journal of Medical Sciences
Original article title: Impact of Rapid Eye Movement Sleep Deprivation on Pain Behaviour and Oxidative Stress in the Thalamus: Role of Tualang Honey Supplementation
The Malaysian Journal of Medical Sciences (MJMS) is a peer-reviewed, open-access journal published online at least six times a year. It covers all aspects of medical sciences and prioritizes high-quality research.
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Original source:

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Author:

Mohd Shafie ANIS SYAHIRAH, Abd Aziz CHE BADARIAH, Long IDRIS, Siran ROSFAIIZAH, Noordin LIZA


The Malaysian Journal of Medical Sciences:

(A peer-reviewed, open-access journal)

Full text available for: Impact of Rapid Eye Movement Sleep Deprivation on Pain Behaviour and Oxidative Stress in the Thalamus: Role of Tualang Honey Supplementation

Year: 2022 | Doi: 10.21315/mjms2022.29.2.7

Copyright (license): CC BY 4.0


Download the PDF file of the original publication


Summary of article contents:

Introduction

Sleep plays a crucial role in various physiological processes, including growth, neurotransmitter synthesis, and immune response modulation. Insufficient sleep can lead to cognitive impairments, slower reactions, and altered pain sensitivity. The relationship between sleep disturbances and pain is reciprocal, with studies indicating that sleep deprivation can heighten pain perception. This research aimed to explore the correlation between oxidative stress (OS) in the thalamus and pain behaviors in a rapid eye movement (REM) sleep-deprived rat model. The study also assessed the potential mitigating effects of Tualang honey, known for its antioxidant properties.

Pain Behavior and Oxidative Stress

The investigation revealed that REM sleep deprivation significantly increased pain behavior scores in rats, particularly in late-phase responses following formalin injection. Additionally, the levels of key oxidative stress markers—glutathione (GSH), glutathione reductase (GR), and superoxide dismutase (SOD)—decreased, while malondialdehyde (MDA) levels increased significantly in the REM sleep-deprived group compared to controls. Notably, the administration of Tualang honey exhibited a reduction in pain behavior and improved oxidative stress profiles in the thalamus, suggesting a protective effect against the detrimental impacts of sleep deprivation.

Conclusion

The findings underscore the significant correlation between oxidative stress and pain behavior in the context of REM sleep deprivation. Notably, antioxidants in the thalamus displayed an inverse relationship with pain behaviors, while the level of MDA demonstrated a positive correlation. The use of Tualang honey effectively reduced oxidative stress and pain responses, indicating its potential as a therapeutic agent in managing pain and oxidative imbalances resulting from sleep disturbances. This research highlights the importance of understanding the interplay between sleep and oxidative stress in pain modulation.

FAQ section (important questions/answers):

What is the focus of the study on REM sleep deprivation?

The study investigates the correlation between oxidative stress in the thalamus and pain behavior in a rat model subjected to rapid eye movement (REM) sleep deprivation.

How were the rats divided for this experiment?

The rats were divided into four groups: control, REM sleep-deprived for 72 hours, REM sleep-deprived pretreated with Tualang honey, and tank control.

What methods were used to assess pain behavior in rats?

Pain behavior was assessed using the formalin test, which recorded responses to a formalin injection in the right hind paw over one hour.

What were the main findings related to oxidative stress and pain?

The study found that oxidative stress markers were significantly correlated with increased pain behavior scores, indicating a relationship between sleep deprivation, oxidative stress, and pain perception.

Glossary definitions and references:

Scientific and Ayurvedic Glossary list for “REM Sleep Deprivation, Pain, Oxidative Stress, and Tualang Honey”. This list explains important keywords that occur in this article and links it to the glossary for a better understanding of that concept in the context of Ayurveda and other topics.

1) Pain:
Pain is a critical aspect of the human experience and refers to the physical and emotional discomfort we feel in response to injury, illness, or stress. In the context of this study, pain is measured using behavior scores in rats to assess how sleep deprivation affects pain sensitivity and response mechanisms.

2) Honey:
Honey, especially Tualang honey, is known for its various health benefits, including antioxidant and anti-inflammatory properties. In the study, Tualang honey is evaluated for its potential to reduce pain behavior and oxidative stress in the thalamus of rats subjected to REM sleep deprivation.

3) Study (Studying):
The study aims to investigate the relationship between oxidative stress in the thalamus and pain behavior in rats following REM sleep deprivation. Its findings contribute to understanding how sleep affects physiological functions and the implications for pain management and treatment strategies involving antioxidants.

4) Inflammation:
Inflammation is the body's response to harmful stimuli, and it plays a crucial role in pain perception. The study assesses inflammation alongside oxidative stress markers to determine their roles in increased pain behavior due to REM sleep deprivation and the effectiveness of Tualang honey in moderating these responses.

5) Table:
Table refers to the organized representation of data. In this study, tables present systematic comparisons of oxidative stress parameters and pain behavior scores across different experimental groups, facilitating easier interpretation of the results and enhancing scientific communication regarding the effects of treatments.

6) Activity:
Activity in this context can refer to the biological or chemical processes occurring in the body as it responds to stimuli. The study measures the activity of various oxidative stress markers in the thalamus and relates this to behavioral responses to assess how sleep deprivation impacts pain.

7) Animal:
Animals, specifically rats in this study, serve as models for understanding complex biological processes. Research involving animal models allows scientists to simulate human physiological responses and test the effects of treatments like Tualang honey on pain and oxidative stress under controlled conditions.

8) Tank:
The tank is used in the REM sleep deprivation model, serving as an environment where rats are prevented from entering REM sleep by the fear of falling into water. This method helps establish effects of sleep deprivation on pain behavior without permanent harm to the animals.

9) Transmission:
Transmission refers to how signals are sent through the nervous system. In the study, the focus is on how oxidative stress and sleep deprivation affect the transmission of pain signals in the thalamus and its relationship to pain behavior during formalin testing.

10) Disease:
While the study does not directly focus on a specific disease, the results may have implications for understanding disease states associated with pain, such as chronic pain disorders. The findings regarding oxidative stress and pain modulation can inform treatment approaches for various inflammatory conditions.

11) Water:
Water serves a dual purpose in the study: as a means to prevent the rats from sleeping (by filling their adaptation tank) and as a necessary component of the animals' environment for hydration. Maintaining hydration is essential for ensuring overall animal well-being during experimentation.

12) Food:
Food references the standard laboratory diet provided to the rats throughout the study. A controlled diet ensures that variables related to nutrition do not confound the results of the experiment and allows for a clearer assessment of how sleep deprivation affects pain behavior.

13) Hind:
Hind refers to the hind paw of the rats, which is used for formalin injection. The response to pain in this area is crucial for measuring pain behavior scores, contributing to the understanding of how sleep deprivation affects pain sensitivity and reactions in the peripheral nervous system.

14) Perception:
Perception in this context relates to how pain is sensed and interpreted by the body. The study examines the impact of REM sleep deprivation on pain perception, aiming to understand how oxidative stress affects the brain's pain processing mechanisms and overall pain sensitivity.

15) Cancer:
Although not the main focus of the study, cancer is mentioned in relation to the importance of understanding pain mechanisms. Chronic pain associated with cancer can be influenced by oxidative stress, making findings regarding the modulation of pain and stress relevant to cancer pain management.

16) Male:
The study exclusively uses male Sprague-Dawley rats as subjects for their experiments. Focusing on a single gender helps eliminate variations in hormonal influences on pain behavior, allowing for a more controlled understanding of the effects of sleep deprivation and treatment interventions.

17) Species:
Species references the specific type of animal used in the study, which are Sprague-Dawley rats. Research on specific species allows for broader understanding and applicability of findings in biomedical research while ensuring accurate representation of similar physiological processes in humans.

18) Glass:
The glass tanks utilized for the REM sleep deprivation model provide a controlled environment for the rats. Glass allows for visibility during observation of behaviors and experimental procedures, lending insight into the studied effects while minimizing outside interferences and maintaining a sterile environment.

19) Flavonoid:
Flavonoids are natural compounds found in Tualang honey that exhibit antioxidant properties. In the context of the study, the relevance of flavonoids underscores the potential benefits of honey as a protective agent against oxidative stress, particularly in relation to pain behavior and neuronal health.

20) Cage:
Cages provide a controlled living environment for the control group of rats in the study. This setup helps minimize stress due to social isolation and ensures that the effects of sleep deprivation can be reliably compared to those in a standard living arrangement.

21) Attending:
Attending refers to the brain's focus and responsiveness during tasks. In the study context, it may relate to how sleep deprivation impacts cognitive functions and attentiveness as participants experience pain, potentially increasing their perception and reporting of pain levels.

22) Shyamala (Syamala):
Shyamala is likely a reference to one of the contributors or researchers associated with the study. Acknowledging authorship is important in scientific publications to recognize individual contributions towards the research and its findings, as well as to maintain accountability for the work presented.

23) Anxiety:
Anxiety, while not the primary focus of this study, may be relevant in discussing the broader psychological and physiological effects of sleep deprivation. Sleep disturbances have been linked to increased anxiety levels, which can exacerbate pain perception and complicate treatment outcomes in chronic pain disorders.

24) Filling (Filled):
Filled refers to the water level maintained in the experimental tanks to prevent the rats from achieving REM sleep. This method is crucial in facilitating the sleep deprivation process while ensuring the safety of the animals during the study's experimental phase.

25) Kumar:
Kumar could pertain to a researcher or author of the study, the mention of which is important for giving credit to contributions in scientific literature. Acknowledging all individuals involved in the research process fosters collaboration and recognition of diverse expertise in the field.

26) Asari:
Asari may refer to another researcher involved in this study. Proper attribution to each contributor emphasizes the collaborative nature of scientific inquiry and provides insight into the team effort typically required for comprehensive research.

27) Alam (Alaṁ):
Alam likely references another researcher associated with the study, critical in highlighting the collaborative dimensions of scientific work. The contribution of each author is important for transparency and indicates the collective effort put into achieving the research objectives.

28) Horn:
Horn could refer to the anatomical structure in rats that relates to their pain pathways, possibly the

Other Science Concepts:

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Discover the significance of concepts within the article: ‘REM Sleep Deprivation, Pain, Oxidative Stress, and Tualang Honey’. Further sources in the context of Science might help you critically compare this page with similair documents:

Pain, Flavonoid, Central nervous system, Spinal Cord, Statistical analysis, Control group, Early phase, Sleep disturbance, Antioxidant activity, Rat model, Experimental group, Anti-inflammatory properties, Analgesic effect, Oxidative stress, Animal model, Anti-inflammatory, Antimicrobial properties, Reactive oxygen species, Pain severity, One-way ANOVA, Immune response, Neurotoxicity, Phenolic content, Inflammatory pain, Antioxidant activities, Glutathione peroxidase, Antioxidant, Malondialdehyde (MDA), Glutathione (GSH), Superoxide dismutase (SOD), Stress, Pain perception, Phosphate-buffered saline, Positive correlation, Antioxidant status, Inflammatory response, Subcutaneous injection, Antitumor properties, Animal research, Neurotransmitter, Hypothalamic-pituitary-adrenal axis, Endothelial function, Sleep Deprivation, Free Radical, Animal Study, Phenolic acid, Catalase (CAT), Oxidative stress biomarkers, Oxidative stress parameters, Monoaminergic system, Neuropathic pain, Intraperitoneal injection, Malondialdehyde Level, Wistar rat, GABAergic neurons, Oral gavage, Glycine, Correlation analysis, Nuclear factor-kappa B, ELISA kit, Glutathione Reductase (GR), MDA level, NMDA receptor, Nociceptive Pain, Formalin injection, Digital analytical balance, GABAergic system, Pain response, Formalin test, Hormonal response, Pearson correlation coefficient, Neurotransmitter release, Inverse correlation, Sodium pentobarbitone, Antioxidant system, Pearson Correlation, Pain modulation, Histological features, Pain pathway, REM sleep, Sensory neurons, Opioid system, Post hoc Bonferroni test, Peripheral inflammation, Phase 2, Signalling pathway, Inflammatory mediator, Glutamate, Extracellular signal regulated kinase, Sprague Dawley rat, Late phase, Nociceptive transmission, Phase II.

Concepts being referred in other categories, contexts and sources.

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