Titia Luise King
- Assistant Professor of Practice
Contact
- (520) 621-9855
- Vet Med Administration
- Oro Valley, AZ 85737
- tluiseking@arizona.edu
Degrees
- Ph.D. Biomedical Sciences
- University of Missouri, Columbia, Missouri, United States
- Neurons projecting to the Paraventricular Nucleus of the Hypothalamus are activated and contribute to cardiorespiratory responses to systemic acute hypoxia
- D.V.M. Veterinary Medicine
- University of Missouri, Columbia, Missouri, United States
- B.S. Animal Science
- University of Missouri, Columbia, Missouri, United States
- Senior Thesis: Effects of Fescue Toxicosis on Physiological Variables
Work Experience
- University of Arizona, Tucson, Arizona (2015 - Ongoing)
- Central Arizona College, Coolidge, Arizona (2014 - 2016)
- Biosphere II, University of Arizona (2014 - 2016)
- Pima Community College, Tucson, Arizona (2014 - 2016)
Awards
- Above and Beyond Award
- ACBS, Spring 2018
Licensure & Certification
- Arizona Veterinary License, Arizona State Veterinary Medical Examing Board (2016)
Interests
Teaching
Anatomy, Physiology, Disease of Companion Animals, Disease of Wildlife, Equine Health Management, Mammalian Histology, Veterinary Pharmacology, One-Health, Laboratory and exotic animal medicine, veterinary medicine
Courses
2024-25 Courses
-
Musculoskeletal
VETM 807 (Spring 2025) -
The Sum of the Parts
VETM 812 (Fall 2024)
2023-24 Courses
-
Gastrointestinal
VETM 809 (Summer I 2024) -
Selectives
VETM 817 (Summer I 2024) -
Musculoskeletal
VETM 807 (Spring 2024)
2022-23 Courses
-
Honors Thesis
ACBS 498H (Spring 2023) -
Musculoskeletal
VETM 807 (Spring 2023) -
ACBS Preceptorship
ACBS 491 (Fall 2022) -
Diseases of Wildlife
ACBS 449 (Fall 2022) -
Diseases of Wildlife
ACBS 549 (Fall 2022) -
Diseases of Wildlife
WFSC 449 (Fall 2022) -
Diseases of Wildlife
WFSC 549 (Fall 2022) -
Honors Thesis
ACBS 498H (Fall 2022) -
Neurobiology and Behavior
VETM 811 (Fall 2022) -
The Sum of the Parts
VETM 812 (Fall 2022)
2021-22 Courses
-
Musculoskeletal
VETM 807 (Spring 2022)
2020-21 Courses
-
Musculoskeletal
VETM 807 (Spring 2021) -
Foundations
VETM 801 (Fall 2020)
2019-20 Courses
-
Anml Anatomy+Physiology
ACBS 400A (Fall 2019) -
Anml Anatomy+Physiology
ACBS 500A (Fall 2019) -
Diseases of Wildlife
ACBS 449 (Fall 2019) -
Diseases of Wildlife
ACBS 549 (Fall 2019) -
Diseases of Wildlife
WFSC 449 (Fall 2019) -
Equine Nutrition+Mgmt
ACBS 431 (Fall 2019) -
Honors Independent Study
ACBS 399H (Fall 2019) -
Honors Thesis
ACBS 498H (Fall 2019)
2018-19 Courses
-
Env Phys Domestic Animal
ACBS 409 (Summer I 2019) -
Independent Study
ACBS 399 (Summer I 2019) -
ACBS Preceptorship
ACBS 491 (Spring 2019) -
Anml Anatomy+Physiology
ACBS 400B (Spring 2019) -
Anml Anatomy+Physiology
ACBS 500B (Spring 2019) -
Diseases/Companion Anmls
ACBS 406 (Spring 2019) -
Independent Study
ACBS 399 (Spring 2019) -
Phys Sci for One Health
ACBS 564B (Spring 2019) -
ACBS Preceptorship
ACBS 491 (Fall 2018) -
Anml Anatomy+Physiology
ACBS 400A (Fall 2018) -
Anml Anatomy+Physiology
ACBS 500A (Fall 2018) -
Diseases of Wildlife
ACBS 449 (Fall 2018) -
Diseases of Wildlife
WFSC 449 (Fall 2018) -
Equine Nutrition+Mgmt
ACBS 431 (Fall 2018) -
Independent Study
ACBS 399 (Fall 2018) -
Intro to Animal Sci Lab
ACBS 102L (Fall 2018) -
Phys Sci for One Health
ACBS 564A (Fall 2018)
2017-18 Courses
-
ACBS Preceptorship
ACBS 491 (Spring 2018) -
Anml Anatomy+Physiology
ACBS 400B (Spring 2018) -
Anml Anatomy+Physiology
ACBS 500B (Spring 2018) -
Diseases/Companion Anmls
ACBS 406 (Spring 2018) -
Intro to Animal Sci Lab
ACBS 102L (Spring 2018) -
Phys Sci for One Health
ACBS 564B (Spring 2018) -
ACBS Preceptorship
ACBS 491 (Fall 2017) -
Anml Anatomy+Physiology
ACBS 400A (Fall 2017) -
Anml Anatomy+Physiology
ACBS 500A (Fall 2017) -
Diseases of Wildlife
ACBS 449 (Fall 2017) -
Diseases of Wildlife
ACBS 549 (Fall 2017) -
Diseases of Wildlife
WFSC 449 (Fall 2017) -
Diseases of Wildlife
WFSC 549 (Fall 2017) -
Equine Nutrition+Mgmt
ACBS 431 (Fall 2017) -
Intro to Animal Sci Lab
ACBS 102L (Fall 2017) -
Phys Sci for One Health
ACBS 564A (Fall 2017)
2016-17 Courses
-
ACBS Preceptorship
ACBS 491 (Spring 2017) -
Anml Anatomy+Physiology
ACBS 400B (Spring 2017) -
Diseases/Companion Anmls
ACBS 406 (Spring 2017) -
Env Phys Domestic Animal
ACBS 409 (Spring 2017) -
ACBS Preceptorship
ACBS 491 (Fall 2016) -
Anml Anatomy+Physiology
ACBS 400A (Fall 2016) -
Diseases of Wildlife
ACBS 449 (Fall 2016) -
Diseases of Wildlife
ACBS 549 (Fall 2016) -
Diseases of Wildlife
WFSC 449 (Fall 2016) -
Diseases of Wildlife
WFSC 549 (Fall 2016) -
Equine Nutrition+Mgmt
ACBS 431 (Fall 2016)
2015-16 Courses
-
ACBS Preceptorship
ACBS 491 (Spring 2016) -
Anml Anatomy+Physiology
ACBS 400B (Spring 2016) -
Anml Anatomy+Physiology
ACBS 500B (Spring 2016) -
Diseases/Companion Anmls
ACBS 406 (Spring 2016)
Scholarly Contributions
Chapters
- King, T. L. (2021). INTEGUMENT AND MAMMARY GLAND/UDDER. In Comparative Veterinary Anatomy A Clinical Approach. Elsevier.
Journals/Publications
- Lago-Alvarez, Y., Podico, G., Segabinazzi, L. G., Cunha, L. L., Barbosa, L., Arnold, C. E., Lima, F. S., King, L. T., McLean, A. K., & Canisso, I. F. (2020). Donkey Epididymal Transport for Semen Cooling and Freezing. Animals : an open access journal from MDPI, 10(12).More infoThe objectives of this study were to assess the cooling and freezing of donkey epididymal semen harvested immediately after castration (Experiment 1, = 4) or after the shipment (24 or 48 h) of epididymides attached to testicles (Experiment 2, = 14) or dissected apart (Experiment 3, = 36). In each experiment, semen was frozen immediately (Non-Centrif) in an egg yolk-based semen extender (EY) or after processing through cushion-centrifugation (Centrif) while extended in a skim milk-based extender (SC). In all three experiments, cooled, pre-freeze, and post-thaw epididymal semen was assessed for total motility (TM), progressive motility (PM), plasma membrane integrity (PMI), and high mitochondrial membrane potential (HMMP). Data were analyzed with R using mixed models and Tukey's test as posthoc. Results showed that the cooling of epididymal semen up to 24 h after harvesting did not affect motility parameters or plasma membrane integrity; furthermore, in Experiment 3, the post-thaw evaluation of both Centrif and Non-Centrif achieved similar TM and PM. Collectively, the post-thaw results revealed low motility parameters across groups; while, the PMI and HMMP did not reflect this trend, and the values remained high, suggesting that there was a lack of epididymal sperm activation with either centrifugation or extenders. In summary, freshly harvested and cooled-shipped and cooled semen had satisfactory semen parameters. Future studies need to address donkey epididymal semen fertility in mares and jennies.
- King, T. L., Ruyle, B. C., Kline, D. D., Heesch, C. M., & Hasser, E. M. (2015). Catecholaminergic neurons projecting to the paraventricular nucleus of the hypothalamus are essential for cardiorespiratory adjustments to hypoxia.. Am J Physiol Regul Integr Comp Physiol..
- King, T. L., Kline, D. D., Ruyle, B. C., Heesch, C. M., & Hasser, E. M. (2013). Acute systemic hypoxia activates hypothalamic paraventricular nucleus-projecting catecholaminergic neurons in the caudal ventrolateral medulla. American journal of physiology. Regulatory, integrative and comparative physiology, 305(10), R1112-23.More infoHypoxia activates catecholamine neurons in the caudal ventrolateral medulla (CVLM). The hypothalamic paraventricular nucleus (PVN) modulates arterial chemoreflex responses and receives catecholaminergic projections from the CVLM, but it is not known whether the CVLM-PVN projection is activated by chemoreflex stimulation. We hypothesized that acute hypoxia (AH) activates PVN-projecting catecholaminergic neurons in the CVLM. Fluoro-Gold (2%, 60-90 nl) was microinjected into the PVN of rats to retrogradely label CVLM neurons. After recovery, conscious rats underwent 3 h of normoxia (21% O2, n = 4) or AH (12, 10, or 8% O2; n = 5 each group). We used Fos immunoreactivity as an index of CVLM neuronal activation and tyrosine hydroxylase (TH) immunoreactivity to identify catecholaminergic neurons. Positively labeled neurons were counted in six caudal-rostral sections containing CVLM. Hypoxia progressively increased the number of Fos-immunoreactive CVLM cells (21%, 19 ± 6; 12%, 49 ± 2; 10%, 117 ± 8; 8%, 179 ± 7; P < 0.001). Catecholaminergic cells colabeled with Fos immunoreactivity in the CVLM were observed following 12% O2, and further increases in hypoxia severity caused markedly more activation. PVN-projecting CVLM cells were activated following more severe hypoxia (10% and 8% O2). A large proportion (89 ± 3%) of all activated PVN-projecting CVLM neurons were catecholaminergic, regardless of hypoxia intensity. Data suggest that catecholaminergic, PVN-projecting CVLM neurons are particularly hypoxia-sensitive, and these neurons may be important in the cardiorespiratory and/or neuroendocrine responses elicited by the chemoreflex.
- King, T. L., Heesch, C. M., Clark, C. G., Kline, D. D., & Hasser, E. M. (2012). Hypoxia activates nucleus tractus solitarii neurons projecting to the paraventricular nucleus of the hypothalamus. American journal of physiology. Regulatory, integrative and comparative physiology, 302(10), R1219-32.More infoPeripheral chemoreceptor afferent information is sent to the nucleus tractus solitarii (nTS), integrated, and relayed to other brain regions to alter cardiorespiratory function. The nTS projects to the hypothalamic paraventricular nucleus (PVN), but activation and phenotype of these projections during chemoreflex stimulation is unknown. We hypothesized that activation of PVN-projecting nTS neurons occurs primarily at high intensities of hypoxia. We assessed ventilation and cardiovascular parameters in response to increasing severities of hypoxia. Retrograde tracers were used to label nTS PVN-projecting neurons and, in some rats, rostral ventrolateral medulla (RVLM)-projecting neurons. Immunohistochemistry was performed to identify nTS cells that were activated (Fos-immunoreactive, Fos-IR), catecholaminergic, and GABAergic following hypoxia. Conscious rats underwent 3 h normoxia (n = 4, 21% O(2)) or acute hypoxia (12, 10, or 8% O(2); n = 5 each). Hypoxia increased ventilation and the number of Fos-IR nTS cells (21%, 13 ± 2; 12%, 58 ± 4; 10%, 166 ± 22; 8%, 186 ± 6). Fos expression after 10% O(2) was similar whether arterial pressure was allowed to decrease (-13 ± 1 mmHg) or was held constant. The percentage of PVN-projecting cells activated was intensity dependent, but contrary to our hypothesis, PVN-projecting nTS cells exhibiting Fos-IR were found at all hypoxic intensities. Notably, at all intensities of hypoxia, ∼75% of the activated PVN-projecting nTS neurons were catecholaminergic. Compared with RVLM-projecting cells, a greater percentage of PVN-projecting nTS cells was activated by 10% O(2). Data suggest that increasing hypoxic intensity activates nTS PVN-projecting cells, especially catecholaminergic, PVN-projecting neurons. The nTS to PVN catecholaminergic pathway may be critical even at lower levels of chemoreflex activation and more important to cardiorespiratory responses than previously considered.
- Kline, D. D., King, T. L., Austgen, J. R., Heesch, C. M., & Hasser, E. M. (2010). Sensory afferent and hypoxia-mediated activation of nucleus tractus solitarius neurons that project to the rostral ventrolateral medulla. Neuroscience, 167(2), 510-27.More infoThe nucleus tractus solitarius (nTS) of the brainstem receives sensory afferent inputs, processes that information, and sends projections to a variety of brain regions responsible for influencing autonomic and respiratory output. The nTS sends direct projections to the rostral ventrolateral medulla (RVLM), an area important for cardiorespiratory reflexes and homeostasis. Since the net reflex effect of nTS processing ultimately depends on the properties of output neurons, we determined the characteristics of these RVLM-projecting nTS neurons using electrophysiological and immunohistochemical techniques. RVLM-projecting nTS neurons were identified by retrograde tracers. Patch clamp analysis in the horizontal brainstem nTS slice demonstrated that RVLM-projecting nTS cells exhibit constant latency solitary tract evoked excitatory postsynaptic currents (EPSCs), suggesting they receive strong monosynaptic contacts from visceral afferents. Three distinct patterns of action potential firing, associated with different underlying potassium currents, were observed in RVLM-projecting cells. Following activation of the chemoreflex in conscious animals by 3 h of acute hypoxia, 11.2+/-1.9% of the RVLM-projecting nTS neurons were activated, as indicated by positive Fos-immunoreactivity. Very few RVLM-projecting nTS cells were catecholaminergic. Taken together, these data suggest that RVLM projecting nTS neurons receive strong monosynaptic inputs from sensory afferents and a subpopulation participates in the chemoreflex pathway.
Other Teaching Materials
- King, T. L. (2023. WHERE THE WILD DOGS ARE: A CASE STUDY ON ALPHA FEMALE DOMINANCE IN AFRICAN WILD DOGS. University of Arizona.