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    Vagus Nerve Stimulation and Anxiety
    Vagus Nerve Stimulation and Anxiety
    Vagus Nerve Stimulation and Anxiety
    Ebook112 pages3 hours

    Vagus Nerve Stimulation and Anxiety

    By Taunjah P. Bell Ph.D.

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    About this ebook

    In 1997, Vagus Nerve Stimulation (VNS) therapy (Cyberonics, Houston, Texas) was approved by the United States Food and Drug Administration for the treatment of epilepsy refractory to antiepileptic medications. In 2005, VNS received FDA approval for treatment-resistant depression refractory to antidepressants, and Cyberonics recently received FDA approval for the clinical study of VNS for rapid cycling bipolar depression. Many researchers continue to investigate the anxiolytic effects of VNS in human and non-human animal models. The author presents a study of VNS effects on anxiety and the capacity of atropine methyl nitrate to attenuate these effects. The results indicate that VNS decreases anxiety in the laboratory animals tested. These findings provide evidence to support the testing and subsequent use of VNS therapy for the treatment of clinical anxiety in humans. Because many therapies that are effective in the treatment of depression effectively treat anxiety, VNS therapy should be effective and approvable for clinical anxiety. This book can serve as a research tool, training mechanism, or surgical guide to the implantation of the vagus nerve stimulating electrode in the laboratory rat. Hopefully, this resource provides information that facilitates FDA approval of VNS for treatment-resistant anxiety, a chronic, devastating and often debilitating illness.
    LanguageEnglish
    PublisheriUniverse
    Release dateAug 5, 2010
    ISBN9781450242875
    Vagus Nerve Stimulation and Anxiety
    Author

    Taunjah P. Bell Ph.D.

    Taunjah P. Bell earned a Doctorate of Philosophy from Southern Illinois University where she specialized in Behavioral Neuroscience. Dr. Bell is now a Visiting Assistant Professor in the Department of Psychology at Jackson State University (JSU) where she teaches Physiological Psychology, Experimental Psychology, Learning, and Statistics. She also serves as Research Advisor and leads the Anxiety Study Group in JSUs Psychology Department. The author developed this group to design research and involve students in the study of physiological factors associated with psychological indicators of anxiety, fear and related emotions. Dr. Bells research interests include investigating VNS effects on anxiety and depression; neurobiological mechanisms underlying emotional control and responses; impairments in neural mechanisms leading to exaggerated fear and anxiety as well as novel treatments for clinical anxiety and depression. In her spare time, the author who is from Miami, Florida, enjoys spending time with Everett, Kate, Bo and Jo.

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      Book preview

      Vagus Nerve Stimulation and Anxiety - Taunjah P. Bell Ph.D.

      Contents

      Preface

      Acknowledgements

      Contributors

      Chapter 1 Introduction

      Chapter 2 Methods

      2.1. Animals

      2.2. Design and construction of the vagus nerve stimulating electrodes

      2.3. Vagus nerve stimulating electrode implantation surgery

      2.4. Vagus nerve stimulation head post preparation

      2.5. Electrode impedance testing

      2.6. Pre-test locomotor response ratings

      2.7. Drug administration and stimulation presentation

      2.8. Behavioral testing procedure

      2.9. Behavioral testing apparatus

      Chapter 3 Results

      3.1. Open field results

      3.2. Elevated plus-maze results

      3.3. Predator scent exposure task results

      Chapter 4 Discussion

      4.1. Goals of the present research

      4.2. Summary of the findings

      4.3. Directions for future research

      4.4. Limitations of the present research

      Chapter 5 Conclusion

      References

      Preface

      PREFACE

      The amygdala is the principle brain region implicated in the processing of fearful stimuli. In rats, distinct amygdalar pathways have been delineated for fear, a relatively brief, stimulus-specific response, and anxiety, a more sustained response prompted by conditions of unpredictable danger (Davis 1998; Davis, 2000; Davis, 2006). When anxiety becomes excessive and sustained in humans, it constitutes a disorder that is debilitating and difficult to treat. Previous research conducted in our laboratory suggested that in addition to enhancing memory processes, electrical stimulation of the vagus nerve in rats also attenuates anxiety-related behaviors. The purpose of the current research was to explore further the capacity of vagus nerve stimulation (VNS) to attenuate behaviors associated with anxiety. Another goal was to determine whether VNS (1.0 mA; 0.5 ms biphasic pulse width; 20 Hz; 30 sec train) produces its effects by activating descending parasympathetic efferent fibers. If a subcutaneous injection (0.1 mg/kg; 0.5 mg/kg; 1.0 mg/kg) of atropine methyl nitrate (AMN, a cholinergic muscarinic receptor antagonist that does not cross the blood-brain barrier) attenuated the effects of VNS, this finding would suggest that VNS acts by causing an increase in parasympathetic tone, specifically an increase in vagal tone.

      One week before behavioral testing, 96 male Long-Evans rats were implanted with a bipolar stimulating electrode. After the recovery period, animals received two days of baseline testing on each of three measures of anxiety: open field, elevated plus-maze, and predator scent exposure task. Five minutes before each baseline session, the animal was placed in a shock box and a mild footshock (0.75 mA; 1.0 sec) was delivered to induce anxiety. On Day Three, 30 minutes prior to testing, each animal was administered either saline or AMN while unrestrained in its home cage. Twenty minutes later, VNS or sham stimulation was delivered via the head post while the animal moved freely in its home cage. Drug and stimulation effects were examined using a between-subjects multivariate analysis of variance (MANOVA) to analyze the mean scores of Day Three data. The results indicated that VNS had a robust and significant effect on all nine target behaviors measured. Atropine methyl nitrate at the high dose, and in some cases at the medium dose, had some capacity to attenuate the effects of VNS on most target behaviors. Rats administered AMN and no stimulation showed more anxiety than saline-treated sham-stimulated animals. These results provide strong support for the hypothesis that VNS attenuates anxiety.

      Acknowledgements

      ACKNOWLEDGEMENTS

      I am truly thankful for the life that I have and eternally grateful for the opportunities that I have been given. I have been blessed in so many ways and have benefited from my academic and personal experiences on so many levels. Without my faith in God and the help of my family, significant other (Dr. Everett G. Neasman), dogs (Kate, Maya, Bo, and Jo), and so many special people in my life, I would not be where I am today. In particular, I must express my heartfelt appreciation to my significant other. Without Everett’s love, advice, guidance, support, reassurance, and patience, my entire graduate and early professional career would have been even more difficult and quite unbearable. I will always be indebted to him for the sacrifices he has made to support my endeavors.

      I also would like to extend my love, appreciation, and gratitude to my parents, Cleo Bell (mother) and Frank Bell, Sr. (father, deceased). I am truly grateful for the sacrifices they have made through the years so that I could achieve my academic, professional, and personal goals. Although my father is no longer with us, I am sure he would be very proud of my accomplishments. Their love, guidance, support, and commitment throughout the years are what have given me the strength and confidence to get where I am today. The journey has not been easy, but the experience has been worth everything I have endured. I know that the completion of this book is a milestone that my relatives, Everett’s family (especially his parents Lydia J. Neasman and Farley B. Neasman, Sr.), our friends, neighbors, church members, mentors, and colleagues are proud of and I want them all to know they have been instrumental in my success.

      In addition, I am genuinely appreciative of the valuable direction, compassionate advice, and professional expertise of my mentor Dr. Robert A. Jensen. I wish everyone had the opportunity to work with someone with such a passion for science and a zest for life. Dr. Jensen has contributed a great deal to ensure that this research was completed and my goals were accomplished. He has a genuine concern for others and his support has made all the difference in the world. I also would like to thank Dr. Jensen’s neighbors’ cat (Nemo) for donating the feline scent by wearing the cat collars used on Day Three of behavioral testing in the predator scent exposure task.

      Furthermore, I extend my appreciation to Dr. Douglas C. Smith, Dr. Eric A. Jacobs, Dr. David G. Gilbert, and Dr. Thomas C. Calhoun for their individual expertise, recommendations, and guidance. Moreover, I would like to thank Dr. Smith for his involvement in this endeavor and the contribution of his laboratory space and equipment. I also would like to thank Dr. Jacobs for allowing me the opportunity to work in his laboratory during my first year at Southern Illinois University Carbondale and gain knowledge of handling animals, conducting behavioral testing, reviewing literature, and designing experiments that I would not have gained otherwise. In addition, I would like to thank Dr. Gilbert and Dr. Calhoun for their time, advice, careful reading, and dedication to this project. By providing guidance and offering professional advice, Dr. Calhoun who is currently the Chair of the Sociology Department at Jackson State University

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