Brittany N. Dugger 1, John A. Morris 1, Cynthia L. Jordan 1,2, S. Marc Breedlove 1,2 1 Neuroscience Program; 2 Department of Psychology Michigan State.

Slides:



Advertisements
Similar presentations
Topic 18 Sex and the Brain Lange
Advertisements

Sex Differentiation and Dimorphism
Chapter 11 Reproductive Behaviors
Adult Women With Shorter Digit Ratios Rate Boy-Typed Toys More Favorably Dennis Goff, Shi Hua, & Jillian Barlowe Randolph College If preference for gender.
EFFECTS OF EXOGENOUS ESTROGEN AND TESTOSTERONE ON REPRODUCTIVE STRUCTURES AND SPERMATOGENESIS IN THE MALE RAT Ryan Olney 1, Anna Ballard 2, Cyndi Goberdhan.
Alison Bell Animal Biology University of Illinois
Chapter 13 Hormones and Sex
Jamie A. Johansen 1, D. Ashley Monks 3, S. Marc Breedlove 1,2, Cynthia L. Jordan 1,2 1 Neuroscience Program, 2 Department of Psychology Michigan State.
Jamie A. Johansen 1, D. Ashley Monks 3, S. Marc Breedlove 1,2, Cynthia L. Jordan 1,2 1 Neuroscience Program, 2 Department of Psychology Michigan State.
Sex and the Brain.
Regulation of brain-derived neurotrophic factor (BDNF) and tyrosine receptor kinase b (trkB) by androgens in the motoneurons of the spinal nucleus of the.
Adolescence and Puberty
Chapter 17 Sex and the Brain
MCB 135E Discussion GSI: Jason Lowry September 27- October 1.
Chapter 17 Sex and the Brain
Intraspecific Variation in Reproductive Behavior and Morphology in the Male Green Anole Lizard (Anolis carolinensis) Joseph R. Vandecar 1, Michele A. Johnson.
Chapter 10 Reproductive Behaviors
Sex Differentiation and Dimorphism
Love is All We Need: Sex, gender, and sexual orientation.
Hormones and Sexuality – Part 1
SEXUAL DIMORPHISMS IN HUMAN BRAIN (Swaab et al., Hormones and Behavior, 2001.
Chapter Eleven Reproductive Behaviors
Hormones & Sexual Behavior
SEXUAL DIMORPHISMS IN NERVE TISSUE and EXPERIMENTAL MODELS
Introduction Indwelling urinary catheters are used frequently in various settings such as hospitals, nursing homes, acute care hospitals, and in extended.
Significance of DHT Androgen receptor has a higher affinity for DHT Can get effects with low levels of circulating testosterone Secondary sex characteristic.
Chapter 18 Development Sexual Differentiation.
Hormones, Sexual Development, & Sexual Behavior Lecture 11.
The Effect of Fraternal Birth Order on Motor Coordination: Developing a Model for Autism, Attention Deficit/Hyperactivity Disorder, and Dyslexia Allison.
HUMAN SEXUAL DEVELOPMENT AND PARAPHILIAS Prof. MUDr. Jiří Raboch, DrSc. Department of Psychiatry, First Faculty of Medicine, Charles University and General.
Hormones & Sexual Development Lecture 25. Sex, & Gender n Sex l biological differences l male & female l intersex n Gender l self-identity about sex role.
Jamie A. Johansen 1, S. Marc Breedlove 1,2, Cynthia L. Jordan 1,2 1 Neuroscience Program, 2 Department of Psychology, Michigan State University
Animal Science 434 Reproductive Physiology
STEROID EFFECTS ON SDN-POA The sexually dimophic nucleus of the preoptic area (SDN-POA) of rat is larger in male than in female. Perinatal treatments of.
 Anabolic Response to Testosterone in Transgenic Mice with Knocked-down Androgen Receptor in Skeletal Muscle Fibers Cindy D. Knaff, Douglas A. Monks,
Joy Garrett Katy Lenz Aaron Wilber
Hormones & Sexual Development Lecture 23. Sexual Dimorphism n Two forms l male and female n What determines your sex? ~
Damian G. Zuloaga ¹, John A. Morris ², Cynthia L. Jordan ¹, ², S. Marc Breedlove ¹, ² ¹Department of Psychology; ² Neuroscience Program Michigan State.
Brain or Behavioral Sex. Brain and Behavioral Sex Differentiation Gonadal Steroid Hormones Brain Structure Sexual Behavior Genetics Experience.
Seasonal plasticity in the telencephalon of a non-songbird the Ruffed Grouse (Bonasa umbellus). Andrew N. Iwaniuk, Justin M. Krilow Introduction Seasonal.
Dose Response Study of Masculinizing Effects of Estradiol (E 2 ) Student Goals: -to see if we can replicate sex differences -to gauge the sensitivity of.
Hormones & Sexual Behavior Lecture 26. Sexual Behavior: Rats n Controlled by sex hormones n Female l Proceptive ear wiggling, darting, hopping l Receptive.
Ahmed et al. (2008). Pubertal hormones modulate the addition of new cells to sexually dimorphic brain regions. Ahmed et al. (2008). Pubertal hormones modulate.
Females are Genetic Mosaics Female mammals “turn off” one entire X chromosome in each cell early in development =XCI Not perfect up to 20% of X genes escape.
By: Steven Nim Dr. Gorman PSYC 132.  Our paper is about:  1) pubertal affects of hormones affecting the organization of the brain at adolescent  2)
Neural organization under hormonal versus direct-genetic effects Cynthia J. Gill, Ph.D. Asst. Professor of Physiology Hampshire College School of Natural.
The Effects of Choline Supplementation and Brain-Derived Neurotrophic Factor (BDNF) on Hippocampal Volume Changes as a Measurement of Depression Leigh.
BRYAN CURRIE BRAIN DEVELOPMENT OF YOUTH HDFS 892 MICHIGAN STATE UNIVERSITY Biological Causes for the Homosexual Brain.
Research on the relationship between childhood sleep problems and substance use in adolescents and young adults is limited. This knowledge gap has been.
Motivation. Hunger Three hunger factors –Biological –Psychosocial –Genetic.
Motivation and Work Chapter 12 notes 12-4 (obj 12-16)
Biological influences on gender
Sexual Differentiation Berthold’s Experiment (1849)
Significance of DHT Androgen receptor has a higher affinity for DHT
Sex Differentiation and Dimorphism
CELLULAR CHARACTERIZATION OF ANDROGEN RECEPTORS AND STEROID RECEPTOR COACTIVATOR-1 IN THE LEVATOR ANI AND EXTENSOR DIGITORUM LONGUS SKELETAL MUSCLES OF.
Medial Amygdalar Aromatase Neurons Regulate Aggression in Both Sexes
Estrogen Masculinizes Neural Pathways and Sex-Specific Behaviors
The Testosterone Two-Step Is Really a Minuet
Gregory Nachtrab, Michael Czerwinski, Kenneth D. Poss  Current Biology 
SPECIFICATION EXPLAINED
Integrin α1β1 protects against signs of post-traumatic osteoarthritis in the female murine knee partially via regulation of epidermal growth factor receptor.
Volume 16, Issue 17, Pages (September 2006)
S Rasika, Arturo Alvarez-Buylla, Fernando Nottebohm  Neuron 
Franck Mauvais-Jarvis, Arthur P. Arnold, Karen Reue  Cell Metabolism 
Number of ΔFosB-ir cells in the NAc core and shell is dependent on pubertal testosterone and sexual experience. Number of ΔFosB-ir cells in the NAc core.
Immunohistochemistry for P450 aromatase in male frog brain.
Gdx rats exhibit increased BDNF-ir in the MF pathway.
Brief History of the Field
Presentation transcript:

Brittany N. Dugger 1, John A. Morris 1, Cynthia L. Jordan 1,2, S. Marc Breedlove 1,2 1 Neuroscience Program; 2 Department of Psychology Michigan State University, East Lansing, MI Introduction Methods Literature Cited ResultsConclusions Acknowledgments Androgens Maintain Soma Size in the Sexually Dimorphic Nucleus of the PreOptic Area of Adult Male Rats Figure 5. Mean unilateral SDN-POA volume for male rats subjected to either castration or sham surgery. Figure 1. (A) Nissl stain of a 40µm coronal section of an adult male sacrificed 28 days after sham surgery taken with a 4X objective. Abbreviations: SDN-POA, Sexually Dimorphic Nucleus of the PreOptic Area; AC, Anterior Commissure; OC, Optic Chiasm; 3V, Third Ventricle. (B) Higher magnification view of somas (arrows) within the SDN-POA taken with a 100X oil objective. Volume- The PreOptic Area (POA) is involved in sexual and maternal behaviors. Volume of the Sexually Dimorphic Nucleus of the POA (SDN-POA) is larger in wildtype males than in females (Gorski et al. 1978). In male rats with a dysfunctional androgen receptor (AR) (rendering them androgen insensitive) the volume is similar to that of wildtype males. Suggesting that AR plays no role in determining this sex difference. Data suggests that the volume of the SDN-POA is controlled by the hormonal environment during the perinatal period (Dohler et al., 1982). Soma Size- Surprisingly, soma size in the SDN-POA of androgen insensitive genetic male rats is significantly reduced compared to their wildtype male littermates, and is not significantly different from that of their normal female littermates (Morris et al. 2005). Question- Do androgens in adulthood affect soma size in the SDN- POA? Male Soma Size - The reduced soma size of adult males 28 days after castration suggests that androgens are needed to maintain soma size in adult male rats. Unlike SDN-POA volume, testosterone acts both in adulthood and perinatally to masculinize the SDN-POA soma size. Female Soma Size – Testosterone treatment can masculinize female SDN-POA soma size in adulthood. This result suggests that the female SDN-POA soma size retains a sensitivity to testosterone in adulthood. Male SDN-POA Volume- Castration in adulthood does not affect SDN-POA volume in adult male rats. This further supports the idea that SDN-POA volume is determined perinatally. Female SDN-POA Volume- Surprisingly, testosterone may affect SDN-POA volume in adult females. This result suggests that SDN-POA volume of female rats may retain a capacity to respond to androgens after the perinatal period. Thanks to all members of the Breedlove/Jordan lab for their support and assistance. Supported by NIH grant MH Figure 4. Average SDN-POA soma size for male rats subjected to either castration or sham surgery. Figure 3. Mean unilateral SDN-POA volume for ovariectomized female rats given either testosterone (T) filled or blank Silastic capsules. Figure 2. Average SDN-POA soma size for ovariectomized female rats given either testosterone filled or blank Silastic capsules. Gorski RA et al Evidence for a morphological sex difference within the medial preoptic area of the rat brain. Brain Res 148: Dohler KD, et al Differentiation of the sexually dimorphic nucleus in the preoptic area of the rat brain is determined by the perinatal hormone environment. Neurosci Lett. 33(3): Morris JA, et al Partial demasculinization of several brain regions in adult male (XY) rats with a dysfunctional androgen receptor gene. J Comp Neurol. 487(2): Females Testosterone masculinizes female SDN-POA somas in adulthood. Males Soma size is decreased in adult males 28 days after castration. SDN-POA Soma Size Males Castration does not affect SDN-POA volume in adult males. Table 1. Male and female Long Evans rats 60 days of age were sacrificed at 14 or 28 days after the noted treatment or surgery. All females were ovariectomized at 60 days of age. SDN-POA volume was measured using a 5X objective every 80µm in Nissl stained material using Stereoinvestigator Software (Microbrightfield). 6-8 somas were sampled per section throughout the rostal caudal extent of the nucleus with a 63X objective using the optical fractionator probe (range of somas per animal ). SDN-POA Volume Females Testosterone may affect SDN-POA volume in adult females. Contact Information: