
Dr. David Krantz
· Professor in Residence, Department of Psychiatry and Biobehavioral SciencesVerifiedUniversity of California, Los Angeles · Neuroscience
Active 1985–2026
About
Dr. David Krantz is Professor in Residence in the Department of Psychiatry and Biobehavioral Sciences at the David Geffen School of Medicine at UCLA. He completed his undergraduate studies at Brown University and earned an MD/PhD through the Medical Scientist Training Program at UCLA in 1991, where he performed his dissertation on Drosophila eye development with Larry Zipursky. Following a residency in psychiatry at UCLA, he was awarded a Howard Hughes Postdoctoral Fellowship for Physicians to investigate the regulation of vesicular neurotransmitter transporters in Robert Edwards’ laboratory at UCSF. Since returning to UCLA in 2000, Dr. Krantz has been using Drosophila as a model organism to study how changes in the function of neurotransmitter transporters influence synaptic transmission and behavior.
Research topics
- Medicine
- Psychology
- Psychiatry
- Audiology
- Neuroscience
- Internal medicine
- Physical medicine and rehabilitation
- Biology
- Physics
Selected publications
Neuropsychopharmacology · 2026-01-07
articleOpen accessRepetitive Transcranial Magnetic Stimulation (rTMS) engages brain networks for the treatment of Major Depressive Disorder (MDD), using either rhythmic (e.g., 10 Hz) or patterned (e.g., intermittent Theta Burst, or iTBS) stimulation protocols. The distinct effects of these protocols on brain function are not well understood. Sixteen subjects with MDD underwent a TMS-electroencephalography (TMS-EEG) "interrogation" paradigm, in which a broad range of rhythmic and patterned stimulation frequencies were administered in a randomized order to the left dorsolateral prefrontal cortex (L-DLPFC). rTMS-induced changes in oscillatory activity and effective connectivity to the DLPFC were examined at each frequency. Linear mixed-effects models revealed widespread changes in power and connectivity, with magnitude and regional distribution of change dependent upon both protocol and frequency of stimulation. Increases in beta band power were most prominent with patterned stimulation, while rhythmic stimulation increased both alpha and beta power at stimulation frequencies greater than 7 Hz (p < 0.05). Source localization showed that patterned and rhythmic stimulation elicited activation in distinct subregions of the cingulate. Rhythmic and patterned stimulation also had distinct effects on connectivity: notably, only rhythmic stimulation increased connectivity with regions near the stimulation site, while only patterned stimulation decreased connectivity to the left precuneus. Both protocols increased the effective connectivity to the orbitofrontal cortex in the theta and beta response bands (p < 0.05). These results indicate that rhythmic and patterned rTMS engage distinct brain regions in a protocol- and frequency-dependent manner. Future studies should examine how these mechanistic differences may relate to clinical outcomes.
Journal of Affective Disorders · 2026-02-18
articleTranscranial magnetic stimulation . · 2026-02-14
articleOpen access<h2>Abstract</h2> Major Depressive Disorder (MDD) presents with heterogeneous symptom profiles. While repetitive Transcranial Magnetic Stimulation (rTMS) treatment is known to improve depressive symptoms overall, it remains unclear how rapidly individual symptoms that are rated as severe at baseline improve during a clinical course. We analyzed Inventory of Depressive Symptomatology Self-Rated (IDS-SR) data collected every five sessions during rTMS treatment of 741 patients with treatment-refractory depression (TRD). Symptoms were grouped into Somatic-Vegetative (S-V) or Affective-Cognitive (A-C) domains, and analyses were restricted to baseline-severe items (IDS-SR item score ≥2) on a within-patient basis to reduce floor effects. Linear mixed-effects models examined symptom trajectories across domains, and we quantified time to 50% sustained improvement for individual symptoms. S-V symptoms improved slightly faster than A-C symptoms early in treatment (sessions 5 and 10; p < 0.01), but differences between symptom domains were small in comparison to overall change over time and symptom domains converged by the end of treatment. Symptoms that improved earlier were more likely to achieve 50% sustained improvement throughout the course. These real-world data primarily inform expectation-setting: patients can anticipate generalized improvement across baseline-severe symptoms during a full rTMS course, with at most modest early differences between symptom domains.
Research Square · 2025-08-19
preprintOpen accessThe effect of older age on outcomes of rTMS treatment for treatment-resistant depression
International Psychogeriatrics · 2024-03-25 · 17 citations
articleOpen accessClinical outcomes of repetitive transcranial magnetic stimulation (rTMS) for treatment of treatment-resistant depression (TRD) vary widely and there is no mood rating scale that is standard for assessing rTMS outcome. It remains unclear whether TMS is as efficacious in older adults with late-life depression (LLD) compared to younger adults with major depressive disorder (MDD). This study examined the effect of age on outcomes of rTMS treatment of adults with TRD. Self-report and observer mood ratings were measured weekly in 687 subjects ages 16-100 years undergoing rTMS treatment using the Inventory of Depressive Symptomatology 30-item Self-Report (IDS-SR), Patient Health Questionnaire 9-item (PHQ), Profile of Mood States 30-item, and Hamilton Depression Rating Scale 17-item (HDRS). All rating scales detected significant improvement with treatment; response and remission rates varied by scale but not by age (response/remission ≥ 60: 38%-57%/25%-33%; <60: 32%-49%/18%-25%). Proportional hazards models showed early improvement predicted later improvement across ages, though early improvements in PHQ and HDRS were more predictive of remission in those < 60 years (relative to those ≥ 60) and greater baseline IDS burden was more predictive of non-remission in those ≥ 60 years (relative to those < 60). These results indicate there is no significant effect of age on treatment outcomes in rTMS for TRD, though rating instruments may differ in assessment of symptom burden between younger and older adults during treatment.
2024-01-10
peer-review1st authorCorrespondingG3 Genes Genomes Genetics · 2024-01-19 · 9 citations
articleOpen accessSenior authorAminergic signaling is known to play a critical role in regulating female reproductive processes in both mammals and insects. In Drosophila, the ortholog of noradrenaline, octopamine, is required for ovulation as well as several other female reproductive processes. Two octopamine receptors have already been shown to be expressed in the Drosophila reproductive tract and to be required for egg-laying: OAMB and Octβ2R. The Drosophila genome contains 4 additional octopamine receptors-Octα2R, Octβ1R, Octβ3R, and Oct-TyrR-but their cellular patterns of expression in the reproductive tract and potential contribution(s) to egg-laying are not known. In addition, the mechanisms by which OAMB and Octβ2R regulate reproduction are incompletely understood. Using a panel of MiMIC Gal4 lines, we show that Octα2R, Octβ1R, Octβ3R, and Oct-TyrR receptors are not detectable in either epithelium or muscle but are clearly expressed in neurons within the female fly reproductive tract. Optogenetic activation of neurons that express at least 3 types of octopamine receptors stimulates contractions in the lateral oviduct. We also find that octopamine stimulates calcium transients in the sperm storage organs and that its effects in spermathecal, secretory cells, can be blocked by knock-down of OAMB. These data extend our understanding of the pathways by which octopamine regulates egg-laying in Drosophila and raise the possibility that multiple octopamine receptor subtypes could play a role in this process.
Journal of Neuroscience · 2024-06-27 · 16 citations
articleOpen accessSenior authorTo visualize the cellular and subcellular localization of neuromodulatory G-protein–coupled receptors in Drosophila , we implement a molecular strategy recently used to add epitope tags to ionotropic receptors at their endogenous loci. Leveraging evolutionary conservation to identify sites more likely to permit insertion of a tag, we generated constitutive and conditional tagged alleles for Drosophila 5-HT1A , 5-HT2A , 5-HT2B , Oct β 1R , Oct β 2R , two isoforms of OAMB , and mGluR . The conditional alleles allow for the restricted expression of tagged receptor in specific cell types, an option not available for any previous reagents to label these proteins. We show expression patterns for these receptors in female brains and that 5-HT1A and 5-HT2B localize to the mushroom bodies (MBs) and central complex, respectively, as predicted by their roles in sleep. By contrast, the unexpected enrichment of Octβ1R in the central complex and of 5-HT1A and 5-HT2A to nerve terminals in lobular columnar cells in the visual system suggest new hypotheses about their functions at these sites. Using an additional tagged allele of the serotonin transporter, a marker of serotonergic tracts, we demonstrate diverse spatial relationships between postsynaptic 5-HT receptors and presynaptic 5-HT neurons, consistent with the importance of both synaptic and volume transmission. Finally, we use the conditional allele of 5-HT1A to show that it localizes to distinct sites within the MBs as both a postsynaptic receptor in Kenyon cells and a presynaptic autoreceptor.
Journal of Psychiatric Research · 2024-09-21 · 4 citations
articleFrontiers in Molecular Neuroscience · 2024-08-02 · 7 citations
articleOpen accessSenior authorCorrespondingAminergic nuclei in mammals are generally composed of relatively small numbers of cells with broad projection patterns. Despite the gross similarity of many individual neurons, recent transcriptomic, anatomic and behavioral studies suggest previously unsuspected diversity. Smaller clusters of aminergic neurons in the model organism Drosophila melanogaster provide an opportunity to explore the ramifications of neuronal diversity at the level of individual cells. A group of approximately 10 tyraminergic/octopaminergic neurons innervates the female reproductive tract in flies and has been proposed to regulate multiple activities required for fertility. The projection patterns of individual neurons within the cluster are not known and it remains unclear whether they are functionally heterogenous. Using a single cell labeling technique, we show that each region of the reproductive tract is innervated by a distinct subset of tyraminergic/octopaminergic cells. Optogenetic activation of one subset stimulates oviduct contractions, indicating that the cluster as a whole is not required for this activity, and underscoring the potential for functional diversity across individual cells. Using whole cell patch clamp, we show that two adjacent and morphologically similar cells are tonically inhibited, but each responds differently to injection of current or activation of the inhibitory GluCl receptor. GluCl appears to be expressed at relatively low levels in tyraminergic/octopaminergic neurons within the cluster, suggesting that it may regulate their excitability via indirect pathways. Together, our data indicate that specific tyraminergic/octopaminergic cells within a relatively homogenous cluster have heterogenous properties and provide a platform for further studies to determine the function of each cell.
Recent grants
NIH · $644k · 2005
Models of Neuromodulatory Circuits in Drosophila
NIH · $2.1M · 2018–2025
Identification of the Kenyon Cell Neurotransmitter
NIH · $424k · 2016–2018
The Influence of Neurotransmitter Transport on Aminergic Neuromodulation
NIH · $1.9M · 2015–2020
Training in Molecular Toxicology
NIH · $4.0M · 2008–2026
Frequent coauthors
- 48 shared
Andrew F. Leuchter
- 38 shared
Nathaniel D. Ginder
Neurobehavioral Systems
- 34 shared
Robert H. Edwards
University of California, San Francisco
- 32 shared
Ian A. Cook
The Master's Seminary
- 27 shared
Reza Tadayonnejad
Neurobehavioral Systems
- 27 shared
Jennifer G. Levitt
- 22 shared
Andrew C. Wilson
University of Colorado Boulder
- 22 shared
Nikita Vince-Cruz
Awards & honors
- H.W. Magoun Distinguished Lectureship
- Samuel Eiduson Student Lectureship
- Arnold Scheibel Distinguished Fellow in Neuroscience Lecture
- Community Scholars Awards
- Eva Kavan Prize
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