Effects of Dorsal Raphe Inactivation and Stimulation on Morphine CPP
Journal name: The Malaysian Journal of Medical Sciences
Original article title: Effects of Temporary Inactivation and Electrical Stimulation of the Dorsal Raphe Nucleus on Morphine-induced Conditioned Place Preference
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.
This page presents a generated summary with additional references; See source (below) for actual content.
Original source:
This page is merely a summary which is automatically generated hence you should visit the source to read the original article which includes the author, publication date, notes and references.
Gholam Reza GHAVIPANJEH, Ali Asghar POURSHANAZARI, Hojjatllah ALAEI, Sara KARIMI, Meghdad Abarghouei NEJAD
The Malaysian Journal of Medical Sciences:
(A peer-reviewed, open-access journal)
Full text available for: Effects of Temporary Inactivation and Electrical Stimulation of the Dorsal Raphe Nucleus on Morphine-induced Conditioned Place Preference
Year: 2015
Copyright (license): CC BY 4.0
Download the PDF file of the original publication
Summary of article contents:
Introduction
The dorsal raphe nucleus (DRN) is a brain region known for its vital role in regulating various behaviors and reward functions. This study investigates how electrical stimulation and reversible inactivation of the DRN affect morphine-induced conditioned place preference (CPP) in Wistar rats. Using techniques including stereotaxic implantation of electrodes and cannulas in the DRN, the researchers aimed to better understand the influence of the DRN on the reward pathways associated with morphine, a common opioid that produces addictive behaviors.
Impact of DRN Stimulation on Morphine-Induced CPP
One significant finding of this study was that electrical stimulation of the DRN at a specific current intensity (100 μA) influenced the expression and acquisition phases of morphine-induced CPP differently. The stimulation combined with an effective dose of morphine (2.5 mg/kg) significantly reduced the time spent in the drug-paired chamber during the expression phase, suggesting a diminished reward response. Conversely, when paired with an ineffective dose of morphine (0.5 mg/kg), the stimulation led to increased time in the drug-paired chamber during the acquisition phase. These results indicate that DRN stimulation can potentiate the effects of morphine under certain conditions while inhibiting its rewarding effects in others, highlighting the complex role of this nucleus in modulating reward signals.
Conclusion
The findings imply that the DRN's electrical stimulation may alter the concentration of neurotransmitters such as serotonin and potentially affect dopamine release in related brain regions involved in reward processing. This suggests that modulation of the DRN has the potential to influence both the acquisition and expression phases of drug-seeking behavior. Overall, the study contributes to a deeper understanding of how the DRN interacts with opiate-induced behaviors, offering insight into the underlying mechanisms of addiction and the potential for therapeutic interventions targeting this neural circuitry.
FAQ section (important questions/answers):
What is the role of the dorsal raphe nucleus (DRN)?
The dorsal raphe nucleus (DRN) influences various behaviors and reward functions, particularly through the modulation of serotonin levels. It is involved in regulating sleep-wake cycles, appetite, locomotion, emotion, social behavior, and learning, as well as reward-related behaviors.
How does electrical stimulation of the DRN affect morphine-induced CPP?
Electrical stimulation of the DRN with an effective dose of morphine significantly reduced the expression duration of conditioned place preference (CPP). Conversely, it enhanced the acquisition phase when paired with an ineffective dose of morphine.
What methods were used for evaluating DRN's effects on CPP?
The study utilized electrical stimulation and reversible inactivation via lidocaine, with varying morphine doses to assess their impact on different phases of conditioned place preference (CPP) in rats.
What findings were observed regarding morphine doses and CPP?
Only the 2.5 mg/kg dose of morphine significantly enhanced CPP. The study's results indicated that the response to morphine on CPP was not dependent on dose, as no consistent dose-dependent relationship was found.
Glossary definitions and references:
Scientific and Ayurvedic Glossary list for “Effects of Dorsal Raphe Inactivation and Stimulation on Morphine CPP”. 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) Drug:
The term 'Drug' refers to a substance that alters physiological functions and can have therapeutic effects or lead to addiction. In the context of the study, morphine is investigated for its impact on conditioned place preference (CPP) in rats, illustrating how certain drugs can influence behavior and reward systems.
2) Learning:
Learning is the process through which organisms acquire new, or modify existing information or behaviors. This study examines how electrical stimulation of the dorsal raphe nucleus affects learning-related behaviors associated with morphine administration, highlighting the link between neurobiological mechanisms in the brain and learned rewarding experiences.
3) Animal:
Animal subjects, particularly Wistar rats in this research, are utilized for the study of drug effects. Animal models are crucial for understanding drug action and behavioral responses, allowing researchers to explore physiological and psychological phenomena in a controlled environment that informs potential human applications in pharmacology and psychology.
4) Table:
In scientific research, a 'Table' often refers to a data presentation format that organizes information systematically for analysis. Although not explicitly mentioned, the study presumably uses tables to summarize findings, including behavioral data and statistical results, facilitating clearer interpretation and comparison of the effects observed in various treatment groups.
5) Study (Studying):
The term 'Study' represents the systematic investigation into a specific subject, in this instance, the effects of dorsal raphe nucleus stimulation on morphine-induced conditioned place preference. Studies provide empirical evidence to understand behavioral and neurochemical interactions, contributing to a broader understanding of addiction and treatment mechanisms.
6) Pharmacology:
Pharmacology is the branch of medicine concerned with the study of drug actions and interactions in biological systems. This research explores pharmacological effects of morphine and lidocaine on conditioned place preference in rats, providing insights into underlying mechanisms of drug addiction and potential therapeutic approaches to mitigate addiction behavior.
7) Activity:
Activity in this context pertains to the behavioral responses of rats during the conditioned place preference test. It involves measuring the time spent in compartments associated with drug administration to infer reward mechanisms. The study assesses locomotor activity and how it correlates with addiction and reward learning processes.
8) Relative:
Relative refers to the comparative relationship between factors or groups in a study. In this research, various doses of morphine and the effects of electrical stimulation on rats' behaviors are compared, emphasizing how changes in treatment parameters influence conditioned place preference outcomes and contribute to the understanding of reward processing.
9) Pharmacological:
Pharmacological relates to the study of drugs and their effects. In this research, pharmacological interventions like morphine and lidocaine are examined to understand their influence on behavior, particularly how pharmacologically induced changes in neurotransmission affect conditioned place preference and learning associated with drug rewards.
10) Discussion:
Discussion refers to the part of a research paper where findings are interpreted, contextualized within existing literature, and implications are considered. In this study, the discussion would analyze the impact of the results involving drug effects on behavior and potential mechanisms, enriching the scientific understanding of addiction.
11) Science (Scientific):
Science encompasses the systematic study of the natural world through observation and experimentation. The current study exemplifies scientific inquiry into the neurobehavioral effects of drugs, contributing to the broader field of neuroscience and pharmacology, ultimately advancing knowledge about drug addiction and its treatment.
12) Water:
Water is essential for life and often serves as a control substance in behavioral experiments involving animals. In the context of this study, water denotes the conditions under which animals are housed and hydrated, a critical factor in maintaining health and influencing behavioral outcomes in drug-related research.
13) Hand:
The term 'Hand' may refer to manual interactions or techniques employed in administering treatments. In the context of this research, it signifies the careful manipulation required during surgical procedures to implant electrodes and cannulas in rats, ensuring precise delivery of electrical stimulation or pharmacological agents.
14) Transmission:
Transmission relates to the process by which signals or substances are conveyed within the body. This research highlights the role of neurotransmitter transmission in the dorsal raphe nucleus and its influence on conditioned place preference, thus underscoring the importance of understanding neurochemical communication in addiction and behavioral responses.
15) Disease:
Disease refers to a disorder of structure or function in a living organism. In this study, the term underscores the context of addiction, which can be viewed as a disease of the brain influenced by pharmacological agents, requiring effective treatment strategies to alter pathological behaviors related to substance use.
16) House:
House typically denotes the environment in which the animals are kept. The housing conditions are crucial for behavioral experiments as they provide a controlled setting that mitigates external variables, such as stress and nutrition, pivotal for obtaining reliable and valid behavioral responses during the study.
17) Jacob:
Jacob may refer to a researcher or contributor in the context of the study, highlighting collaborative efforts in scientific research. The contributions of various authors are essential for producing comprehensive findings and advancing understanding in fields like pharmacology and neuroscience, particularly concerning addiction.
18) Alam (Alaṁ):
Alam likely refers to a co-author or researcher involved in the study. The acknowledgment of various researchers emphasizes the collaborative nature of scientific inquiry. Researchers work together to investigate complex phenomena, thus improving the reliability and depth of findings in interdisciplinary studies on drug behavior.
19) Food:
Food represents a primary motivator in behavioral studies involving rewards. In conditioned place preference research, the presentation of palatable food can serve as a control or comparator to drug-induced preferences, providing insights into the reward pathways shared by natural and drug-related stimuli in the brain.
20) Pari:
Pari could refer to an individual involved in the research, such as a scientist or assistant whose work supports the study's outcomes. Individual contributions are vital in academic research, ensuring comprehensive data gathering and analysis, and facilitating advancements in the understanding of pharmacological effects on behavior.
21) Wall:
Wall may refer to the physical barriers in the apparatus used for conditioned place preference experiments. These walls define separate environments where behaviors are observed and measured, influencing the spatial learning patterns of rats in response to drug exposure, which is critical in assessing reward-induced behaviors.
22) Pain:
Pain signifies a significant area of investigation, particularly with substances like morphine, which are used for pain relief. Understanding how pain influences behavior and reward systems is fundamental in both addiction research and the development of effective therapeutic measures to manage pain without fostering dependency.
23) Post:
Post often indicates the aftermath or subsequent analysis following experimental procedures. In this study, it might refer to post-treatment observations, where researchers analyze the impacts of the administered drugs or electrical stimulation on behavior, reinforcing the need for thorough evaluation of treatment effects on conditioned responses.
24) Ter:
Ther may refer to therapeutic aspects related to the use of drugs like morphine. In the context of the study, reflecting on therapeutics involves examining how understanding the pharmacological effects on behavior can lead to improved treatment strategies for addiction and effective pain management approaches.
25) Calculation:
Calculation refers to the statistical analysis conducted to interpret the gathered data in the research. Accurate calculations are essential to assess the significance of the experimental findings, such as measuring time spent in specific compartments, which reveals underlying behavioral patterns linked to drug effects and preferences.
26) Euphoria:
Euphoria relates to the intense feelings of pleasure frequently associated with drug use, especially opioids like morphine. This research examines how euphoria influences conditioned place preference, shedding light on the behavioral implications of rewarding experiences tied to drug administration and the neurobiological mechanisms involved.
27) Craving (Crave, Craved):
Craving is the overwhelming desire for a substance, often a key focus in addiction studies. The research explores how electrical stimulation and drug exposure alters craving behaviors in rats, providing insights into the neurochemical and behavioral dynamics that underpin addiction and the maintenance of substance-seeking behavior.
28) Desire:
Desire is closely linked to motivation in the context of drug use, contributing to compulsive behaviors in addiction. This study investigates how morphine administration affects desire-driven behaviors, particularly in relation to conditioned place preference, which is vital for understanding the motivations behind drug-seeking activities.
29) Arrow:
Arrow may symbolize direction or influence in the research context. In behavioral experiments, it could represent cues that guide or signal rats' movements toward specific locations within the apparatus. Understanding how arrows or cues function helps clarify the mechanisms of learning and reward association in addiction.
30) Sign:
Sign may refer to indicators or measures used to evaluate outcomes in the study. Within a behavioral context, signs can help researchers understand the extent of conditioned preferences or cravings in response to drug exposure, thus enhancing the interpretation of data regarding the mechanisms of addiction.
31) Male:
Male signifies the gender of the animal subjects used in this study, specifically Wistar rats. Gender can influence physiological and behavioral responses to drugs, and using male subjects helps control for potential variances, ensuring that findings are focused on the pharmacological effects and behaviors being studied.
Other Science Concepts:
Discover the significance of concepts within the article: ‘Effects of Dorsal Raphe Inactivation and Stimulation on Morphine CPP’. Further sources in the context of Science might help you critically compare this page with similair documents:
Rat, Emotional regulation, Saline Group, Statistical analysis, Significant difference, One-way ANOVA, 5-hydroxytryptamine, Animal house, Effective dose, Emotion regulation, Lidocaine, Neuronal activity, Electrical stimulation, Dopamine release, Working memory, Prefrontal Cortex, Subjective evaluation, Withdrawal Syndrome, Memory formation, Drug addiction, Drug abuse, Motor activity, Self-administration, Locomotor activities, Morphine, Serotonin-Dopamine Interaction, Conditioned place preference, Ventral Tegmental Area, Nucleus Accumbens, Reference memory, Serotonin release, Cholinergic receptors, Motor control, Passive avoidance learning, Morphine-induced CPP, Morphine group, Addiction pathways, Glutamate transmission, Morphine Administration, Saline injection, Serotonin neurotransmission, Behavioral procedure, Opioid drug.
Concepts being referred in other categories, contexts and sources.
Expression, Acquiring, Future reward.