Oculocardiac Reflex and Autonomic Modulation in a Broad-Snouted Caiman (Caiman latirostris)

Authors

DOI:

https://doi.org/10.22456/1679-9216.144013

Keywords:

bradycardia, crocodilian, heart rate, heart rate variability, vago-vagal reflex

Abstract

Background: The oculocardiac reflex (OCR) is a neurophysiological response mediated by the vagus nerve, triggering changes in heart rate and rhythm in response to pressure applied to the ocular globe. While well-documented in humans and other mammals, the OCR remains less explored in reptiles, particularly crocodilians. Given the rising interaction between wildlife and urban settings, understanding OCR in these species has become essential due to potential implications in veterinary and wildlife medicine. This case report aimed to investigate the OCR in a broad-snouted caiman rescued from an urban environment, providing insights into its autonomic responses under ocular compression.

Case: A juvenile broad-snouted caiman, approximately 45 cm in length and weighing 0.8 kg, was rescued from an urban household in Capanema, Paraná, Brazil. The animal, found in a dehydrated and lethargic state far from its natural habitat, was transported to the Wildlife Animal Service at the veterinary hospital of the Federal University of Fronteira Sul (UFFS), Realeza campus, for evaluation and possible release. The animal underwent electrocardiogram (ECG) monitoring using an INcardio X® device (INpulse, Florianópolis, SC, BR) to assess changes in heart rate and rhythm during ocular pressure, simulating vagal stimulation. Surface cup electrodes coated with conducting gel were placed on the animal’s cranial and caudal limbs for ECG readings. Application of ocular pressure induced a notable OCR response, evidenced by a 47% decrease in heart rate, dropping from 34 bpm to 16 bpm, along with changes in heart rate variability (HRV) parameters and a 2nd-degree atrioventricular block. Three min after the release of ocular pressure, the heart rate returned to 29 bpm, with HRV values returning to baseline, indicating a recovery of autonomic balance.

Discussion: Manual restraint in crocodilians often involves ocular pressure to facilitate temporary immobilization through vagal activation. However, the OCR poses substantial cardiovascular risks, as highlighted by this case. During OCR activation, HRV metrics such as Standard Deviation of NN intervals (SDNN) and Root Mean Square of Successive Differences (RMSSD) rose, reflecting increased heart rate variability likely due to heightened parasympathetic activity. Additionally, increases in the mean NN interval and the Cardiac Vagal Index (CVI) pointed to enhanced vagal modulation, while a drop in the Cardiac Sympathetic Index (CSI) indicated diminished sympathetic response. Changes in DFA parameters with increased α-1 and decreased α-2 values reflected short-term variability and reduced long-term complexity, respectively. These shifts underscored a significant autonomic imbalance dominated by parasympathetic tone. The atrioventricular block and multiple sinoatrial node depolarizations observed during the OCR response align with known reptilian cardiac responses to parasympathetic dominance. Similar findings have been reported in canine studies during OCR, suggesting that vagal modulation of HRV may share patterns across taxa. The results of this report underline the necessity of safety precaution for handling of crocodilians during ocular manipulation, as failure to recognize OCR could result in severe bradycardia, arrhythmias, or even cardiac arrest. Future studies should expand on the physiological implications of OCR in crocodilians, as insights from these investigations will be critical for veterinary practices involving these animals. This report provides pioneering data on HRV and OCR in a caiman, offering valuable perspectives for improving welfare and safety protocols in wildlife and veterinary care.

Keywords: bradycardia, crocodilian, heart rate, heart rate variability, vago-vagal reflex.

Downloads

Download data is not yet available.

References

Barreto-Lima A.F., Rodrigues M.P.L., Costa F.R.F., Filho A.E.M., Campos Y.L., Lima D.C. & Gonzalez R.C. 2023. First record of Caiman latirostris (Daudin, 1802) from the state of Ceará, Northeastern Brazil. Herpetology Notes. 16: 411-414.

Brüler B.C., Vieira T.C., Wolf M., Lucina S.B., Montiani-Ferreira F. & Sousa M.G. 2018. Using the Oculocardiac Reflex to Characterize Autonomic Imbalance in a Naturally Occurring Canine Model of Valvular Insufficiency. Comparative Medicine. 68(2): 156-162.

Duran L.M., Taylor E.W., Sanches P.V.W., Cruz A.L., Tavares D., Sartori M.R., Abe A.S. & Leite C.A.C. 2020. Heart rate variability in the tegu lizard, Salvator merianae, its neuroanatomical basis and role in the assessment of recovery from experimental manipulation. Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology. 240: 110607. DOI: 10.1016/j.cbpa.2019.110607 DOI: https://doi.org/10.1016/j.cbpa.2019.110607

Hunt C. 2015. Neurological Examination and Diagnostic Testing in Birds and Reptiles. Journal of Exotic Pet Medicine. 24(1): 34-51. DOI: 10.1053/j.jepm.2014.12.005 DOI: https://doi.org/10.1053/j.jepm.2014.12.005

Jensen B., Vesterskov S., Boukens B.J., Nielsen J.M., Moorman A.F.M., Christoffels V.M. & Wang T. 2017. Morpho-functional characterization of the systemic venous pole of the reptile heart. Scientific Reports. 7(1): 6644. DOI: 10.1038/s41598-017-06291-z DOI: https://doi.org/10.1038/s41598-017-06291-z

Jepson L. 2010. Exotic animal medicine: a quick reference guide. In: Lizards. New York: Elsevier Saunders, pp.268-314

Kerola T., Eranti A., Aro A.L., Haukilahti M.A., Holkeri A., Junttila M.J., Kenttä T. V., Rissanen H., Vittinghoff E., Knekt P., Heliövaara M., Huikuri H.V. & Marcus G.M. 2019. Risk Factors Associated With Atrioventricular Block. JAMA Network Open. 2(5): e194176. DOI: 10.1001/jamanetworkopen.2019.4176 DOI: https://doi.org/10.1001/jamanetworkopen.2019.4176

Micheli M. & Campbell H. 2008. Autonomic control of heart rate exhibits diurnal shifts in a crocodilian. Amphibia-Reptilia. 29(4): 567-571. DOI: 10.1163/156853808786230505 DOI: https://doi.org/10.1163/156853808786230505

Shaffer F. & Ginsberg J.P. 2017. An Overview of Heart Rate Variability Metrics and Norms. Frontiers in Public Health. 5: 1-17. DOI: 10.3389/fpubh.2017.00258 DOI: https://doi.org/10.3389/fpubh.2017.00258

Tarbert D.K., Murthy V.D. & Guzman D.S. 2022. Neurological examination in healthy adult inland bearded dragons (Pogona vitticeps). Journal of the American Veterinary Medical Association. 260(9): 1013-1023. DOI: 10.2460/javma.20.12.0706 DOI: https://doi.org/10.2460/javma.20.12.0706

Turner Giannico A., de Sampaio M.O.B., Lima L., Corona Ponczek C., De Lara F. & Montiani-Ferreira F. 2014. Characterization of the oculocardiac reflex during compression of the globe in Beagle dogs and rabbits. Veterinary Ophthalmology. 17(5): 321-327. DOI: 10.1111/vop.12077 DOI: https://doi.org/10.1111/vop.12077

Valentinuzzi M.E. & Hoff H.E. 1972. The sinus venosus-atrial Wenckebach-Luciani phenomenon. Journal of Electrocardiology. 5(1): 1-14. DOI: 10.1016/S0022-0736(72)80057-8 DOI: https://doi.org/10.1016/S0022-0736(72)80057-8

Vanderlei L.C.M., Pastre C.M., Hoshi R.A., Carvalho T.D. & Godoy M.F. 2009. Noções básicas de variabilidade da frequência cardíaca e sua aplicabilidade clínica. Revista Brasileira de Cirurgia Cardiovascular. 24(2): 205-217. DOI: 10.1590/S0102-76382009000200018 DOI: https://doi.org/10.1590/S0102-76382009000200018

Vézina-Audette R., Steagall P.V.M. & Gianotti G. 2019. Prevalence of and covariates associated with the oculocardiac reflex occurring in dogs during enucleation. Journal of the American Veterinary Medical Association. 255(4): 454-458. DOI: 10.2460/javma.255.4.454 DOI: https://doi.org/10.2460/javma.255.4.454

Vieira T.C.S., Sampaio M.O., Brüler B.C., Ben-Shlomo G., Montiani-Ferreira F. & Duque J. 2023. The effect of eye stimulation using graded external weights on the oculocardiac reflex in beagle dogs. Archives of Veterinary Science. 28(1): 1-6. DOI: 10.5380/avs.v1i1.85932 DOI: https://doi.org/10.5380/avs.v1i1.85932

Yoo J.J., Gishen K.E. & Thaller S.R. 2021. The Oculocardiac Reflex: Its Evolution and Management. Journal of Craniofacial Surgery. 32(1): e80-e83. DOI: 10.1097/SCS.0000000000006995 DOI: https://doi.org/10.1097/SCS.0000000000006995

Yves A., Lima L.M.C., Bassetti L.A.B., Andrade M.B.B., Sousa B.M. & Marques T.S. 2023. Distribution of broad-snouted caiman (Caiman latirostris) in the Rio Doce State Park, Minas Gerais, Brasil. North-Western Journal of Zoology. 19(2): 167-172.

Additional Files

Published

2025-07-09

How to Cite

Rodrigues Marques, A. L., Marangoni, M., Mamguê, V. E., Takazono Lemes, M., Martínez, O., Braz, P. H., & Champion, T. (2025). Oculocardiac Reflex and Autonomic Modulation in a Broad-Snouted Caiman (Caiman latirostris). Acta Scientiae Veterinariae, 53. https://doi.org/10.22456/1679-9216.144013

Similar Articles

<< < 30 31 32 33 34 35 36 37 38 39 > >> 

You may also start an advanced similarity search for this article.