Lucinda L Rankin
- Associate Professor, Educator Scholar Track
- Member of the Graduate Faculty
- (520) 621-3104
- Biological Sciences West, Rm. 000274
- Tucson, AZ 85721
- crankin@arizona.edu
Awards
- Commitment to Excellence , Pima JTED Governing Board Service Award
- Pima JTED School District, Fall 2023
- Pima JTED School District, Fall 2022
- UA Distinguished Outreach Faculty
- Univ of Arizona: nominee sponsored by Physiology, CoM-T and UAHS., Fall 2023 (Award Nominee)
- Maria Teresa Velez Outstanding Faculty Mentoring Award
- UA Commission on the Status of Women, Spring 2020
- 5 Star Teaching Award - finalist
- Honors College, Spring 2019 (Award Finalist)
- Honoray Faculty member
- AED Leadership Fraternity, Spring 2019
- Excellence in Teaching and Mentoring
- UA Honors College, Spring 2017
- UA BlueChip Program Certificate of Appreciation Mentoring Award
- UA BlueChip Program, Fall 2016
- UA BlueChip Program, Fall 2015
- Tucson Women of Influence: Education Champion
- Inside Tucson Business, Spring 2016 (Award Finalist)
- Carpe Diem Award
- Physiology Club, Spring 2015
- Teaching Fellow - Physiology Education Community of Practice Fellows
- American Physiological Society, Spring 2015
- American Physiological Society, Summer 2014
- Chi Omega Outstanding Faculty
- Chi Omega Honors Sorority, Spring 2014
- Favorite Physiology Professor
- Physiology Club, UA, Spring 2014
- Honorary Faculty Inductee
- Mortar Board National College Senior Honor Society, Spring 2014
- 5-Star Teaching Award
- University of Arizona, Spring 2013 (Award Finalist)
Interests
No activities entered.
Courses
2024-25 Courses
-
Hnrs Precept Physiology
PSIO 391H (Fall 2024) -
Honors Thesis
PSIO 498H (Fall 2024) -
K-8 HCI
NURS 493 (Fall 2024) -
Physio Sci Teaching Wksp
PS 697A (Fall 2024) -
Preceptorship
PSIO 591 (Fall 2024) -
Senior Honors Thesis Prep
PSIO 495H (Fall 2024)
2023-24 Courses
-
Current Topics in Physiology
PSIO 489 (Spring 2024) -
Hnrs Precept Physiology
PSIO 391H (Spring 2024) -
Honors Independent Study
PSIO 499H (Spring 2024) -
Honors Thesis
PSIO 498H (Spring 2024) -
Intro to Honors in Physiology
PSIO 295H (Spring 2024) -
K-8 HCI
NURS 493 (Spring 2024) -
Physio Sci Teaching Wksp
PS 697B (Spring 2024) -
Preceptorship
PSIO 391 (Spring 2024) -
Hnrs Precept Physiology
PSIO 391H (Fall 2023) -
Honors Thesis
PSIO 498H (Fall 2023) -
K-8 HCI
NURS 493 (Fall 2023) -
Physio Sci Teaching Wksp
PS 697A (Fall 2023) -
PhysioConnects B
PSIO 395B (Fall 2023) -
Preceptorship
PSIO 391 (Fall 2023) -
Senior Honors Thesis Prep
PSIO 495H (Fall 2023)
2022-23 Courses
-
Current Topics in Physiology
PSIO 489 (Spring 2023) -
Hnrs Precept Physiology
PSIO 391H (Spring 2023) -
Honors Independent Study
PSIO 399H (Spring 2023) -
Honors Thesis
PSIO 498H (Spring 2023) -
Independent Study
PSIO 499 (Spring 2023) -
Intro to Honors in Physiology
PSIO 295H (Spring 2023) -
Physio Sci Teaching Wksp
PS 697B (Spring 2023) -
PhysioConnects A
PSIO 395A (Spring 2023) -
Preceptorship
PSIO 391 (Spring 2023) -
Hnrs Precept Physiology
PSIO 391H (Fall 2022) -
Honors Thesis
PSIO 498H (Fall 2022) -
Physio Sci Teaching Wksp
PS 697A (Fall 2022) -
PhysioConnects B
PSIO 395B (Fall 2022) -
Preceptorship
PSIO 391 (Fall 2022) -
Senior Honors Thesis Prep
PSIO 495H (Fall 2022)
2021-22 Courses
-
Current Topics in Physiology
PSIO 489 (Spring 2022) -
Hnrs Precept Physiology
PSIO 391H (Spring 2022) -
Honors Thesis
PSIO 498H (Spring 2022) -
Intro to Honors in Physiology
PSIO 295H (Spring 2022) -
Physio Sci Teaching Wksp
PS 697B (Spring 2022) -
PhysioConnects A
PSIO 395A (Spring 2022) -
Preceptorship
PSIO 391 (Spring 2022) -
Hnrs Precept Physiology
PSIO 391H (Fall 2021) -
Honors Thesis
PSIO 498H (Fall 2021) -
Independent Study
PSIO 499 (Fall 2021) -
Physio Sci Teaching Wksp
PS 697A (Fall 2021) -
PhysioConnects B
PSIO 395B (Fall 2021) -
Preceptorship
PSIO 391 (Fall 2021) -
Senior Honors Thesis Prep
PSIO 495H (Fall 2021)
2020-21 Courses
-
Current Topics in Physiology
PSIO 489 (Spring 2021) -
Hnrs Precept Physiology
PSIO 391H (Spring 2021) -
Honors Thesis
PSIO 498H (Spring 2021) -
Independent Study
PSIO 399 (Spring 2021) -
Independent Study
PSIO 499 (Spring 2021) -
Independent Study
PSIO 699 (Spring 2021) -
Intro to Honors in Physiology
PSIO 295H (Spring 2021) -
Physio Sci Teaching Wksp
PS 697B (Spring 2021) -
PhysioConnects A
PSIO 395A (Spring 2021) -
Preceptorship
PSIO 391 (Spring 2021) -
Tackling Physiological Topics
PSIO 101 (Spring 2021) -
Hnrs Precept Physiology
PSIO 391H (Fall 2020) -
Honors Thesis
PSIO 498H (Fall 2020) -
Independent Study
PSIO 499 (Fall 2020) -
Physio Sci Teaching Wksp
PS 697A (Fall 2020) -
PhysioConnects B
PSIO 395B (Fall 2020) -
Preceptorship
PSIO 391 (Fall 2020) -
Senior Honors Thesis Prep
PSIO 495H (Fall 2020) -
Tackling Physiological Topics
PSIO 101 (Fall 2020)
2019-20 Courses
-
Current Topics in Physiology
PSIO 489 (Spring 2020) -
Hnrs Precept Physiology
PSIO 391H (Spring 2020) -
Honors Thesis
PSIO 498H (Spring 2020) -
Independent Study
PSIO 499 (Spring 2020) -
Intro to Honors in Physiology
PSIO 295H (Spring 2020) -
Physio Sci Teaching Wksp
PS 697B (Spring 2020) -
PhysioConnects A
PSIO 395A (Spring 2020) -
Preceptorship
PSIO 391 (Spring 2020) -
Independent Study
PSIO 399 (Winter 2019) -
Hnrs Precept Physiology
PSIO 391H (Fall 2019) -
Honors Thesis
PSIO 498H (Fall 2019) -
Independent Study
PSIO 399 (Fall 2019) -
Independent Study
PSIO 499 (Fall 2019) -
Physio Sci Teaching Wksp
PS 697A (Fall 2019) -
PhysioConnects B
PSIO 395B (Fall 2019) -
Preceptorship
PSIO 391 (Fall 2019) -
Senior Honors Thesis Prep
PSIO 495H (Fall 2019) -
Tackling Physiological Topics
PSIO 101 (Fall 2019)
2018-19 Courses
-
Independent Study
PSIO 499 (Summer I 2019) -
Current Topics in Physiology
PSIO 489 (Spring 2019) -
Hnrs Precept Physiology
PSIO 391H (Spring 2019) -
Honors Thesis
PSIO 498H (Spring 2019) -
Independent Study
PSIO 399 (Spring 2019) -
Independent Study
PSIO 499 (Spring 2019) -
Intro to Honors in Physiology
PSIO 295H (Spring 2019) -
Physio Sci Teaching Wksp
PS 697B (Spring 2019) -
PhysioConnects B
PSIO 395B (Spring 2019) -
Preceptorship
PSIO 391 (Spring 2019) -
Hnrs Precept Physiology
PSIO 391H (Fall 2018) -
Honors Thesis
PSIO 498H (Fall 2018) -
Independent Study
PSIO 499 (Fall 2018) -
Physio Sci Teaching Wksp
PS 697A (Fall 2018) -
PhysioConnects A
PSIO 395A (Fall 2018) -
PhysioConnects B
PSIO 395B (Fall 2018) -
Preceptorship
PSIO 391 (Fall 2018) -
Senior Honors Thesis Prep
PSIO 495H (Fall 2018)
2017-18 Courses
-
Current Topics in Physiology
PSIO 489 (Spring 2018) -
Fundamntls Human Physiol
PSIO 380 (Spring 2018) -
Hnrs Precept Physiology
PSIO 391H (Spring 2018) -
Honors Thesis
PSIO 498H (Spring 2018) -
Independent Study
PSIO 399 (Spring 2018) -
Independent Study
PSIO 499 (Spring 2018) -
Intro to Honors in Physiology
PSIO 295H (Spring 2018) -
Physio Sci Teaching Wksp
PS 697B (Spring 2018) -
PhysioConnects B
PSIO 395B (Spring 2018) -
Preceptorship
PSIO 391 (Spring 2018) -
Hnrs Precept Physiology
PSIO 391H (Fall 2017) -
Honors Thesis
PSIO 498H (Fall 2017) -
Independent Study
PSIO 499 (Fall 2017) -
Physio Sci Teaching Wksp
PS 697A (Fall 2017) -
PhysioConnects A
PSIO 395A (Fall 2017) -
PhysioConnects B
PSIO 395B (Fall 2017) -
Preceptorship
PSIO 391 (Fall 2017) -
Senior Honors Thesis Prep
PSIO 495H (Fall 2017)
2016-17 Courses
-
Current Topics in Physiology
PSIO 489 (Spring 2017) -
Fundamntls Human Physiol
PSIO 380 (Spring 2017) -
Hnrs Precept Physiology
PSIO 391H (Spring 2017) -
Honors Thesis
PSIO 498H (Spring 2017) -
Independent Study
PSIO 399 (Spring 2017) -
Independent Study
PSIO 499 (Spring 2017) -
Intro to Honors in Physiology
PSIO 295H (Spring 2017) -
Physio Sci Teaching Wksp
PS 697B (Spring 2017) -
PhysioConnects B
PSIO 395B (Spring 2017) -
Preceptorship
PSIO 391 (Spring 2017) -
Hnrs Precept Physiology
PSIO 391H (Fall 2016) -
Honors Thesis
PSIO 498H (Fall 2016) -
Independent Study
PSIO 499 (Fall 2016) -
Physio Sci Teaching Wksp
PS 697A (Fall 2016) -
PhysioConnects A
PSIO 395A (Fall 2016) -
PhysioConnects B
PSIO 395B (Fall 2016) -
Senior Honors Thesis Prep
PSIO 495H (Fall 2016) -
Special Topics in Science
HNRS 195I (Fall 2016)
2015-16 Courses
-
Current Topics in Physiology
PSIO 489 (Spring 2016) -
Fundamntls Human Physiol
PSIO 380 (Spring 2016) -
Hnrs Precept Physiology
PSIO 391H (Spring 2016) -
Honors Independent Study
PSIO 499H (Spring 2016) -
Honors Thesis
PSIO 498H (Spring 2016) -
Independent Study
PSIO 499 (Spring 2016) -
Intro to Honors in Physiology
PSIO 295H (Spring 2016) -
Physio Sci Teaching Wksp
PS 697B (Spring 2016) -
Preceptorship
PSIO 391 (Spring 2016)
Scholarly Contributions
Journals/Publications
- DelloRusso, C., Fregosi, R. F., Khurana, N., Rankin, L. L., & Sullivan, J. (2002).
Mechanisms of force failure during repetitive maximal efforts in a human upper airway muscle
. Muscle & Nerve. doi:10.1002/mus.10167More infoThe upper airway respiratory muscles play an important role in the regulation of airway resistance, but surprisingly little is known about their contractile properties and endurance performance. We developed a technique that allows measurement of force and the electromyogram (EMG) of human nasal dilator muscles (NDMs). Endurance performance was quantified by measuring NDM “flaring” force and EMG activity as healthy human subjects performed 10 s maximal voluntary contractions (MVCs), separated by 10 s rest, until the area under the force curve fell to 50% MVC (the time limit of the fatigue task, Tlim), which was reached in 34.2 ± 3.1 contractions (685.0 ± 62.3 s). EMG activity was unchanged except at Tlim, where it averaged 78.7 ± 3.6% of pretest activity (P < 0.01). M-wave amplitude did not change, suggesting that neuromuscular propagation was not impaired. MVC force increased to 80% of the pretest level within 10 min of recovery but twitch force failed to recover, suggesting low-frequency fatigue. The data suggest that a failure of the nervous system to excite muscle could explain at most only a small fraction of the NDM force loss during an intermittent fatigue task, and then only at Tlim. Thus, the majority of the force failure during this task is due to impairment of mechanisms that reside within the muscle fibers. © 2002 Wiley Periodicals, Inc. Muscle Nerve 26: 94–100, 2002 - Allen, R. E., Boxhorn, L. K., Greene, E., Johnson, S. E., Pierce, P. R., Rankin, L. L., & Taylor, R. G. (1991).
Desmin is present in proliferating rat muscle satellite cells but not in bovine muscle satellite cells
. Journal of Cellular Physiology. doi:10.1002/jcp.1041490323More infoThe presence of desmin was characterized in cultured rat and bovine satellite cells and its potential usefulness as a marker for identifying satellite cells in vitro was evaluated. In primary cultures, positive immunohistochemical staining for desmin and skeletal muscle myosin was observed in rat and bovine myotubes. A small number of mononucleated cells (20% of rat satellite cells and 5% of bovine satellite cells) were myosin-positive, indicative of post-mitotic differentiated myocytes. In bovine satellite cell cultures 13% of the mononucleated cells were desmin-positive, while 84% of the mononucleated cells in rat satellite cell cultures were desmin-positive. Rat satellite cell mass cultures and bovine satellite cell clonal density cultures were pulsed with 3H-thymidine, and autoradiographic data revealed that >94% of dividing rat cells were desmin-positive, suggesting that desmin is synthesized in proliferating rat satellite cells. However, no desmin was seen in cells that incorporated labeled thymidine in bovine satellite cell clones. Analysis of clonal density cultures revealed that only 14% of the mononucleated cells in bovine satellite cell colonies were desmin-positive, whereas 98% of the cells in rat satellite cell colonies were desmin-positive. Fibroblast colonies from both species were desmin-negative. In order to further examine the relationship between satellite cell differentiation and desmin expression, 5-bromo-2′-deoxyuridine (BrdU) was added to culture medium at the time of plating to inhibit differentiation. Fusion was inhibited in rat and bovine cultures, and cells continued to divide. Very few desmin-positive cells were found in bovine cultures, but greater than 90% of the cells in rat cultures stained positive for desmin. The presence of desmin and sarcomeric myosin was also evaluated in regenerating rat tibialis anterior five days after bupivicaine injection. In regenerating areas of the muscle many desmin-positive cells were present, and only a few cells stained positive for skeletal muscle myosin. Application of desmin staining to rat satellite cell growth assays indicated that rat satellite cells cultured in serum-containing medium were contaminated with fibroblasts at levels that ranged from approximately 5% in 24 hr cultures to 15% in mature cultures. In defined medium 4 day cultures contain approximately 95% to 98% desmin-positive satellite cells. The effects of combinations of insulin-like growth factor I (IGF-I), basic fibroblast growth factor (bFGF), and transforming growth factor beta (TGF-β) on rat satellite cell proliferation and differentiation were assessed by desmin staining, and results were found to be consistent with results obtained previously using conventional cell staining and counting techniques (Allen and Boxhorn, 1989). Our experiments indicate that the pattern of desmin expression in satellite cells differs between rat and bovine and that desmin can be a useful marker for cultured rat satellite cells. - Allen, R. J., Chartier, L., Fusetani, N., Hartshorne, D. J., Karaki, H., Kato, Y., Rankin, L. L., & Watabe, S. (1991).
Calyculin-A increases the level of protein phosphorylation and changes the shape of 3T3 fibroblasts
. Cytoskeleton. doi:10.1002/cm.970180104More infoCalyculin-A, an inhibitor of type 1 and 2A phosphatases, was applied extracellularly to 3T3 fibroblasts. At 0.1 microM, calyculin-A caused a marked increase in protein phosphorylation in both the cytosolic and insoluble cellular fractions. This effect was independent of external Ca2+. An immunoprecipitate, formed with an antibody to myosin, contained several cytoskeletal components. Increased phosphorylation following treatment with calyculin-A was observed in vimentin, the 20-kD myosin light chain, and an unidentified 440-kD component. An enhanced level of vimentin phosphorylation was found in intermediate filament preparations from treated cells. Calyculin-A also caused marked shape changes of 3T3 cells. Within minutes after addition of calyculin-A (0.1 microM) cells became rounded and lost attachment to the substratum. Stress fibers, intermediate filaments, and microtubules, prominent in the attached control cells, were not evident in the rounded cells. Shape changes were reversible and after removal of calyculin-A the rounded cells attached to the substratum, resumed a flattened shape, and were active mitotically. In the cells treated with calyculin-A an unusual "ball-like" structure was observed with transmission electron microscopy. This unique structure was 2-3 microM in diameter and was located close to the nucleus. The use of calyculin-A adds further support to the idea that cell shape is controlled, at least in part, by concerted actions of a kinase-phosphatase couple. - Allen, R. E., & Rankin, L. L. (1990).
Regulation of Satellite Cells during Skeletal Muscle Growth and Development
. Experimental Biology and Medicine. doi:10.3181/00379727-194-43060More infoSatellite cells are myogenic cells attributed with the role of postnatal growth and regeneration in skeletal muscle. Following proliferation and subsequent differentiation, these cells will fuse with one another or with the adjacent muscle fiber, thereby increasing myonuclei numbers for fiber growth and repair. The potential factors which could regulate this process are many, including exercise, trauma, passive stretch, innervation, and soluble growth factors. Three classes of growth factors in particular (fibroblast growth factor, insulin-like growth factor, and transforming growth factor-beta) have been studied extensively with respect to their effects on satellite cell proliferation and differentiation in culture. Fibroblast growth factor has been shown to stimulate proliferation but depress differentiation. Insulin-like growth factor stimulates both proliferation and differentiation, although the latter to a much greater degree. Transforming growth factor-beta slightly depresses proliferation but inhibits differentiation. When administered in combination, these factors can induce satellite cell activities in culture which mimic those typical of satellite cells found in vivo in growing, regenerating, or healthy mature muscle. Alterations in the concentrations of these growth factors in the muscle environment as well as alterations in the cell's sensitivity or responsiveness to these factors represent potential mechanisms for regulating satellite cell activity in situ. - Enoka, R. M., Rankin, L. L., Stuart, D. G., & Volz, K. A. (1989).
Fatigability of rat hindlimb muscle: associations between electromyogram and force during a fatigue test.
. The Journal of Physiology. doi:10.1113/jphysiol.1989.sp017458More info1. An experimental protocol designed to assess fatigability in motor units (Burke, Levine, Tsairis & Zajac, 1973) has been applied to the whole muscles of anaesthetized adult rats, and the association between the electromyogram (EMG) and force was monitored over the course of the test. 2. Both test muscles (soleus and extensor digitorum longus) exhibited a wide range of fatigability, which was defined as the decline in isometric peak force at 6 min, such that the data could be separated into five levels of fatigability. Fatigue indices for each test muscle were distributed across three levels. 3. The EMG was quantified with four measures of amplitude, four of duration, and one interaction term (area). Correlation analyses indicated that the EMG was adequately represented by one measure of amplitude (absolute amplitude), one of duration (peak-to-peak duration) and area. The best single measure was area. 4. The EMG-force associations for soleus varied markedly among its three fatigability groups. In contrast, over the course of the test, all three extensor digitorum longus groups displayed qualitatively similar EMG-force associations. 5. Multiple regression analyses indicated that the EMG parameters were able to predict peak force better for extensor digitorum longus than for soleus. Furthermore, for both test muscle, the prediction was best for the most fatigable group. 6. The associations between EMG and force exhibited three patterns for the two test muscles and three levels of fatigability. These differences suggested variation in the mechanisms, related to both fibre-type composition and susceptibility to fatigue, that dictate the performance elicited by this particular stimulus regimen. The mechanisms seem to include both intracellular and transmission processes. - Enoka, R. M., Joyner, M. J., Rankin, L. L., & Stuart, D. G. (1988).
Fatigue-related changes in neuromuscular excitability of rat hindlimb muscles
. Muscle & Nerve. doi:10.1002/mus.880111104More infoAbstract Brief repetitive trains of supramaximal nerve stimulation produce intermittent muscle activation and, in time, a progressive decline in force (i.e., neuromuscular fatigue) and depression of the electromyogram (EMG). These changes may include within‐train reductions in EMG due to a failure of neuromuscular propagation. 13 The aim of the present study was to investigate changes in EMG during a 360‐second stimulus regimen designed to fatigue soleus and extensor digitorum longus muscles of anesthetized rats by activating the muscle with repetitive trains of 40 Hz stimuli. Measurements included peak force for each tetanus, variation of the within‐train EMG (coefficient of variation for area), and magnitude of the first EMG waveform (area) of each train. Fatigue was characterized as the relative decline in force over the course of the test. The responses of the test muscles were categorized, based on an absolute scale of fatigability, into five groups: potentiated, nonfatigable, low fatigability, intermediate fatigability, and high fatigability. Fatigable muscles (low, intermediate, and high fatigability groups) demonstrated a decreased EMG magnitude and an increased EMG‐area variation with repetitive activation. This increased variation, however, was nonmonotonically related to fatigability such that the least and most fatigable muscles had the smallest within‐train EMG variation. We suggest that these data can be explained by considering the EMG (compound muscle action potential) as a stochastic process that represents a composite of single‐fiber events (axonal to sarcolemmal transmission) with variable probabillities. - Enoka, R. M., Rankin, L. L., Stuart, D. G., & Volz, K. A. (1988).
Coexistence of twitch potentiation and tetanic force decline in rat hindlimb muscle
. Journal of Applied Physiology, 65(6), 2687-2695. doi:10.1152/jappl.1988.65.6.2687More infoAn experimental protocol designed to assess fatigability in motor units has been applied to two hindlimb muscles of anesthetized adult rats to study the effects of whole-muscle fatigue on the isometric twitch. Both soleus and extensor digitorum longus exhibited a linear relationship between fatigability (i.e., force decline after a 360-s fatigue test) and the magnitude of the twitch force following the fatigue test. Twitch force after the fatigue test was potentiated (i.e., greater than the value before the fatigue test) in many muscles, despite the development of considerable fatigue. This coexistence of fatigue and twitch potentiation was observed in 7% (5/70) of soleus and 48% (31/64) of extensor digitorum longus muscles. The coexistence was exhibited only by the least fatigable muscles of the fast-contracting extensor digitorum longus. The extensor digitorum longus muscles that did not exhibit twitch potentiation probably experienced a higher proportion of muscle-fiber inactivation, such as due to failure of neuromuscular propagation, that was induced by the fatigue regimen. - Enoka, R. M., Joyner, M. J., Rankin, L. L., & Stuart, D. G. (1987).
460
. Medicine and Science in Sports and Exercise. doi:10.1249/00005768-198704001-00460 - Enoka, R. M., Rankin, L. L., & Stuart, D. (1985).
Cage-size and gender effects on fatigue in rats.
. The Physiologist. - Chvapil, M., D, T., Misiorowski, R. L., Rankin, L. L., Stoy, V., & Weinstein, P. (1984).
Development of topical BAPN delivery system for acute spinal cord injury in dogs
. Journal of Biomedical Materials Research. doi:10.1002/jbm.820180706More infoAbstract Topical sustained release of various medications by a subdurally implantable device at the site of spinal cord injury is considered advantageous in the treatment of early symptoms of tissue damage. A typical case is the interference with collagenous scar by β‐aminopropionitrile, inhibiting collagen polymerization. Four materials, silicone, polyethylene, polytetrafluoroethylene (PTFE), and polyacrylonitrile‐based hydrogel were evaluated for biocompatibility in subcutaneous implantations. The hydrogel, the least reactive, was then compared with silicone sheets as subcural implants. The histology favored the hydrogel as the most inert material, which was then used for the construction of soft, pliable pouches, releasing the drug through the hydrated wall at a rate controlled by an osmotic pump. - Chvapil, M., Johnson, P., Misiorowski, R. L., Rankin, L. L., & Weinstein, P. (1983).
Diffusion characteristics of β-aminopropionitrile in peripheral nerve
. Experimental Neurology. doi:10.1016/0014-4886(83)90381-3More infobeta-Aminopropionitrile (beta-APN), a lathyrogen, alters the physical characteristics of fibrous scar tissue and as such may have potential clinical use in treatment of injured spinal cord and peripheral nerve by reducing the physical barrier to axon regeneration. For beta-APN to exert its lathyrogenic effect, it must permeate the injury site and gain access to the developing collagenous scar. To investigate the diffusion characteristics, beta-[14C]APN solution was applied as an immersion bath to rat sciatic nerve using both in vivo and in vitro preparations for intervals of 15 to 90 min. The four experimental groups studied were (a) intact nerve, (b) hemisected nerve, (c) nerve with epineurium removed, and (d) nerve with both epineurium and perineurium removed. The isotope labeling index determined by autoradiography and scintillation counting indicated the perineurium as the primary barrier to significant diffusion of beta-APN in normal nerve. When perineurium was incised or removed, beta-APN entered the endoneurial matrix. beta-APN concentration in the epineurium and perineurium increased with increasing bathing time in vitro; but it decreased markedly after 15 min of in vivo bathing. These findings indicate that topical application of beta-APN to injured peripheral nerve would be a successful method of exposing fibrogenic intraneural tissue to the inhibitory effect on lysyl oxidase enzymes. Continuous application, however, will be necessary because of the rapid beta-APN removal documented in the vivo preparation.
Presentations
- Rankin, L. L., Kanady, J., & Stanescu, C. (2020, Summer). Graduate Teaching Assistant Training Program at the University of Arizona: a 3-pronged approach. Experimental Biology/American Physiological Society. Virtual - due to cancellation of in-person Annual EB Conference: American Physiological Society.More infoSelected presentation for Special Section on "Teaching Trainees to Teach Physiology"
Poster Presentations
- Lessa Sacoman, J., Rankin, L. L., & Ngo, A. (2021, October). Introducing Physiology to Freshmen Students: the PSIO101 Experience. Arizona Physiological Society. Midwestern University, Glendale, Az: APS.
- Ng, A., Rankin, L. L., & Sacoman, J. L. (2021, OCt). Introducing Physiology to Freshmen Students: The PSIO 101 Course Experience at the University of Arizona. Annual Conference, AZ Chapter of American Physiological Society. Glendale AZ: UA.
- Rankin, L. L. (2018, April). The Physiological and Mental Effects of Dance on Health and Rehabilitative Therapy. PSIO Undergraduate Poster session. Tucson Arizona: Dept of Physiology.More infoHonors thesis research poster presentation
- Rankin, L. L. (2018, April). “The role of diet in alleviating gastrointestinal and behavioral symptoms in children with autism”. PSIO Undergraduate Poster Sessin. Tucson Arizona: Dept of Physiology.More infoHonors thesis research poster
- Rankin, L. L. (2018, June). The PhysioWorks Program: Expanding opportunities to put your knowledge to work. 2nd Annual National PMIG Conference. Tucson Arizona: Dept of Physiology.
- Rankin, L. L., & Davis, M. (2016, April). Use of Balance tests as predictors of risks for injury in girls high school basketball players. Physiology Undergraduate Poster Session. University of Arizona: Physiology Department.
- Rankin, L. L., & Dobbins, D. (2016, April). Humor as a complementary therapy: An insight into humor being used as treatment in medicine. Physiology Undergraduate Poster Session. University of Arizona: Physiology Department.
- Rankin, L. L., & Holbrook, C. (2016, April). Assessment of Concussion Awareness in UA Students. Physiology Undergraduate Poster Session. University of Arizona: Physiology Department.