Summary

자발적으로 다이빙 수중에 교육 쥐 : 포유류 다이빙 응답의 조사

Published: November 12, 2014
doi:

Summary

Detailed instructions are provided on how to train rats to voluntarily dive underwater through a 5 m long Plexiglas maze. Because the brains of rats have been very well characterized, voluntarily diving rats may help elucidate the central pathways of the mammalian diving response.

Abstract

Underwater submergence produces autonomic changes that are observed in virtually all diving animals. This reflexly-induced response consists of apnea, a parasympathetically-induced bradycardia and a sympathetically-induced alteration of vascular resistance that maintains blood flow to the heart, brain and exercising muscles. While many of the metabolic and cardiorespiratory aspects of the diving response have been studied in marine animals, investigations of the central integrative aspects of this brainstem reflex have been relatively lacking. Because the physiology and neuroanatomy of the rat are well characterized, the rat can be used to help ascertain the central pathways of the mammalian diving response. Detailed instructions are provided on how to train rats to swim and voluntarily dive underwater through a 5 m long Plexiglas maze. Considerations regarding tank design and procedure room requirements are also given. The behavioral training is conducted in such a way as to reduce the stressfulness that could otherwise be associated with forced underwater submergence, thus minimizing activation of central stress pathways. The training procedures are not technically difficult, but they can be time-consuming. Since behavioral training of animals can only provide a model to be used with other experimental techniques, examples of how voluntarily diving rats have been used in conjunction with other physiological and neuroanatomical research techniques, and how the basic training procedures may need to be modified to accommodate these techniques, are also provided. These experiments show that voluntarily diving rats exhibit the same cardiorespiratory changes typically seen in other diving animals. The ease with which rats can be trained to voluntarily dive underwater, and the already available data from rats collected in other neurophysiological studies, makes voluntarily diving rats a good behavioral model to be used in studies investigating the central aspects of the mammalian diving response.

Introduction

The diving response consists of a suite of autonomic reflexes seen in animals of all vertebrate classes 1. In response to submersion under water, this reflexly-induced response consists of apnea, bradycardia and an alteration of blood flow that maintains flow to the heart, brain and exercising muscles while limiting flow to viscera and non-exercising muscles 2. Many of the metabolic and cardiorespiratory aspects of the mammalian diving response have been well investigated 2,3, including those in humans 4,5. However, what has been relatively lacking, until recently, is investigation of the central integrative aspects of the diving response. What happens within the brainstem, and what is the neuronal step-by-step pathway, that connects afferent inputs to efferent outputs during this autonomic reflex? Answering these questions will require an appropriate animal model 6. An adage in comparative physiology, the Krogh principle 7, is that for every research question there is some animal of choice on which the problem can be most conveniently studied. A most appropriate animal for studying the central aspects of the diving response is the rat 6,8. In large part this is due to the fact that the brains of rats have been very well characterized, both anatomically and functionally, and many rat brain atlases are available 6. Additionally the rat is particularly useful in cardiorespiratory research, because the physiology of the rat is well known across all major organ systems, and the rat is well regarded as an animal model in systems biology 6. Finally, the laboratory rat is the domesticated version of the wild Rattus norvegicus, an animal that routinely swims and dives underwater 6. Based on these considerations, the rat is a good choice for studies investigating the central aspects of the mammalian diving response. In comparison, using marine animals to investigate the central aspects of the mammalian diving response would be much more difficult. This is due in large part to marine animals having comparatively large and non-uniformly sized brains, and the relative difficulty and high cost of housing these animals.

Rats have previously been used to investigate many aspects of the mammalian diving response, primarily in situations involving forced underwater submergence 9-12. However many studies in marine and aquatic animals have shown that there can be a differential response to diving based upon whether the submergence was forced or voluntary 2,13. Diving animals may show an extremely intense bradycardia during forced diving but a much less intense bradycardia during voluntary diving. The “stress” of forced submergence can significantly change the cardiovascular responses of diving in many animals 14. Small rodents such as muskrats also show a more intense diving response during forced submergence than during voluntary diving 15,16. Thus, if rats are to be used to investigate the central aspects of the mammalian diving response, investigators should be aware that a rat forcibly submerged underwater may produce a response different from that of a voluntarily diving rat.

The goal of this article is to provide detailed instructions on how to train rats to voluntarily dive underwater. These procedures are not technically difficult, but can be time-consuming. The training is conducted in such a way as to reduce the stressfulness that could otherwise be associated with forced underwater submergence. This voluntary diving technique should minimize activation of central stress pathways and thus better allow investigation of the central aspects of the diving response. By itself, training rats to voluntarily dive underwater generates no data that can be used to investigate the central aspects of the mammalian diving response. Therefore examples of how voluntarily diving rats have been used in conjunction with other physiological and neuroanatomical research techniques, and how the basic dive training may need to be modified to accommodate theses other techniques, are also provided.

Protocol

참고 : 설명 실험 프로토콜 여기에 중서부 대학에서 실시 중서부 대학 IACUC에 의해 승인되었다. 1. 룸 요구 사항 뜨겁고 차가운 수돗물을 실행했다 절차 방 바닥에, 탱크로부터 통상 드레인 물을 제거하는 방법을 확보. 다이빙 탱크를 배치에 대한 연구 테이블을 사용합니다. 바닥 배수구가있는 방은 일반적으로 배수 윤곽 때문에, 고무 마개를 줄이고 탱크의 테?…

Representative Results

설명 수영과 다이빙 교육 과정의 성공적인 완료는 물에서 다이빙 할 때 쥐가 경험하는 스트레스를 줄일 수 있습니다. 혈액 코르티 코스 테론 수준은 반복적 인 매일 훈련이 자발적 다이빙과 관련된 stressfulness을 감소 함을 표시하고 훈련 된 쥐 인간 (그림 2; 17)에 의해 매일 처리되는 것보다 다이빙이 더 이상 스트레스를 찾을 수 없습니다. 반대로, 다이빙 프로토콜에서 교육을?…

Discussion

자신의 야생 형태의 수에서 쥐와 반 수생 환경을 악용 할, 식품 6 꼴을하면서 의지는 종종 수중 다이빙. 따라서 쥐가 아주 쉽게 자발적으로 수중 다이빙을 훈련 할 수있는 너무 놀라운 일이 아니다. 기술 교육 과정은 대부분의 성인 쥐의 뇌지도 책에 사용되는 신체 사이즈 (~ 300g)에 새로 이유 쥐를 가져올 것이다 육주,까지 지속될 수 있습니다. 이러한 교육을받은 동물 따라서 뇌는 더 쉽게 …

Divulgaciones

The authors have nothing to disclose.

Acknowledgements

연구는 연구 및 스폰서 프로그램의 중서부 대학 사무실에서 자금을 지원. 또한 중서부 대학 동물 시설과 에릭 워렌 감사합니다.

Materials

Name of Material/ Equipment Company Catalog Number Comments/Description
1 in internal diameter tubing  Fisher 14-169-63 Used to fill or drain tank
N95 mask – Moldex #2300N Series Fisher 19-003-246D Used to limit inhalation of rat allergens
Plexiglas rodent restraint device (Economy flat bottomed restrainer) Braintree FB-M/L  For forced dives
Telemetric transmitters  DSI Model PA-C40 (270-0040-008) Used to transmit pulsatile arterial blood pressure
Hand-held antenna wand DSI Model RLA 3000 (272-5007) Used to ensure radio antenna is near to transmitter while rat is negotiating underwater maze
Intramedic PE50, 0.023" ID Fisher 14-170-12B Used as trailing arterial cannula

Referencias

  1. Butler, P. J., Jones, D. R., Lowenstein, O. . Advances in Comparative Physiology and Biochemistry. 8, 179-364 (1982).
  2. Butler, P. J., Jones, D. R. Physiology of diving birds and mammals). Physiol. Rev. 77, 837-899 (1997).
  3. Butler, P. J. Metabolic regulation in diving birds and mammals. Resp. Physiol. Neurobiol. 141, 297-315 (2004).
  4. Foster, G. E., Sheel, A. W. The human diving response, its function, and its control. Scand. J. Med. Sci. Sports. 15, 3-12 (2005).
  5. Lindholm, P., Lundgren, C. E. G. The physiology and pathophysiology of human breath-hold diving. J. Appl. Physiol. 106, 284-292 (2009).
  6. McCulloch, P. F. Animal models for investigating the central control of the mammalian diving response. Front. Physiol. 3, 1-16 (2012).
  7. Krogh, A. The progress of physiology. Am. J. Physiol. 90, 243-251 (1929).
  8. Panneton, W. M., Gan, Q., Juric, R. The rat: a laboratory model for studies of the diving response. J. Appl. Physiol. 108, 811-820 (2010).
  9. Lin, Y. C. Autonomic nervous control of cardiovascular responses during diving in the rat. Am. J. Physiol. 227, 601-605 (1974).
  10. Lin, Y. C., Baker, D. G. Cardiac output and its distribution during diving in the rat. Am. J. Physiol. 228, 733-737 (1975).
  11. Huang, T. F., Peng, Y. I. Role of the chemoreceptors in diving bradycardia in the rat. Jap. J. Physiol. 26, 395-401 (1976).
  12. Fahlman, A., Bostrom, B. L., Dillon, K. H., Jones, D. R. The genetic component of the forced diving bradycardia response in mammals. Front. Physiol. 2, 1-7 (2011).
  13. Blix, A. S., Folkow, B., Shepher, J. T., Abboud, F. M. . Handbook of Physiology. , 917-944 (1984).
  14. Kooyman, G. L. Diverse Divers. 200, (1989).
  15. MacArthur, R. A., Karpan, C. M. Heart rates of muskrats diving under simulated field conditions: persistence of the bradycardia response and factors modifying its expression. Can. J. Zool. 67, 1783-1792 (1989).
  16. McCulloch, P. F., Jones, D. R. Cortical influences on diving bradycardia in muskrats (Ondatra zibethicus). Physiol. Zool. 63, 1098-1117 (1990).
  17. McCulloch, P. F., Dinovo, K. M., Connolly, T. M. The cardiovascular and endocrine responses to voluntary and forced diving in trained and untrained rats. Am. J. Physiol. Regul. Integr. Comp. Physiol. 298, 224-234 (2010).
  18. Panneton, W. M., Gan, Q., Dahms, T. E. Cardiorespiratory and neural consequences of rats brought past their aerobic dive limit. J. Appl. Physiol. 109, 1256-1269 (2010).
  19. Chotiyanonta, J. S., DiNovo, K. M., McCulloch, P. F. Bilateral sectioning of the anterior ethmoidal nerves does not eliminate the diving response in voluntarily diving rats. Physiol. Reports. 1, (2013).
  20. Panneton, W. M., Anch, A. M., Panneton, W. M., Gan, Q. Parasympathetic preganglionic cardiac motoneurons labeled after voluntary diving. Front. Physiol. 5, 1-10 (2014).
  21. McCulloch, P. F., Ollenberger, G. P., Bekar, L. K., West, N. H. Trigeminal and chemoreceptor contributions to bradycardia during voluntary dives in rats. Am. J. Physiol. Regul. Integr. Comp. Physiol. 273, 814-822 (1997).
  22. Ollenberger, G. P., Matte, G., Wilkinson, A. A., West, N. H. Relative distribution of blood flow in rats during surface and submerged swimming. Comp. Biochem. Physiol. A. 119, 271-277 (1998).
  23. Ollenberger, G. P., West, N. H. Distribution of regional cerebral blood flow in voluntarily diving rats. J. Exp. Biol. 201, 549-558 (1998).
  24. McCulloch, P. F. Activation of the trigeminal medullary dorsal horn during voluntary diving in rats. Brain Res. 1051, 194-198 (2005).
  25. Panneton, W. M., et al. Activation of brainstem neurons by underwater diving in the rat. Front. Physiol. 3, 1-13 (2012).
  26. McCulloch, P. F., Panneton, W. M. Activation of brainstem catecholaminergic neurons during voluntary diving in rats. Brain Res. 984, 42-53 (2003).
  27. McCulloch, P. F. Globosa neurons: a distinct subgroup of noradrenergic neurons in the caudal pons of rats. Brain Res. 964, 164-167 (2003).
  28. Panneton, W. M. The mammalian diving response: an enigmatic reflex to preserve life. Physiology. 28, 284-297 (2013).
check_url/es/52093?article_type=t

Play Video

Citar este artículo
McCulloch, P. F. Training Rats to Voluntarily Dive Underwater: Investigations of the Mammalian Diving Response. J. Vis. Exp. (93), e52093, doi:10.3791/52093 (2014).

View Video