Respiration, Acid/Base, Ammonia and Ionoregulatory Strategies in the Pacific hagfish (Eptatretus stoutii)

  • Author / Creator
    Clifford, Alexander M
  • Hagfish feed on putrefied carrion, which poses several environmental challenges to the scavenger including hypoxia (Low PO2), hypercapnia (high PCO2) and high environmental ammonia (HEA). To any other organism, these conditions would be physiologically challenging; however, hagfish seem to have adapted to survive and thrive in this type of environment. While feeding, hagfish immerse their head and gills in the decaying flesh leaving their trunk exterior to the carcass, allowing for potential cutaneous exchange of acid/base (A/B) equivalents, ammonia and O2. Hagfish are osmoconformers and do not regulate plasma [Na+] or [Cl-] but do regulate the divalent ions SO42-, Mg2+ and Ca2+; however, the hormone(s) controlling this regulation have remained elusive. In this thesis, I describe some of the physiological strategies that Pacific hagfish (Eptatretus stoutii) employ to withstand and recover from stresses in A/B status, and exposure to ammonia and hypercapnia. Furthermore I identify the relative branchial and cutaneous contributions to overall maintenance of A/B status, ammonia excretion, and O2 acquisition through the use of custom designed separated-flux chambers. Finally I characterize the glucocorticoid and mineralocorticoid responses of the hagfish and identify the role of the corticosteroids previously shown to act on hagfish corticosteroid receptor. An environment with a high PCO2 will initially cause acidification of the blood followed by compensatory metabolic plasma [HCO3-] elevations. I simulated these perturbations in hagfish through injections of either HCl or NaHCO3 (total H+/HCO3- load: 6000 µmolkg-1). Hagfish excreted the acid load via excretion of acid equivalents in the gill region while the resultant base load was excreted in the skin-only posterior region, indicating that the gills may not be involved in recovery from acute metabolic hypercarbia. However, following chronic hypercapnia exposure (72 h; 0.6% CO2) to induce hypercarbia, hagfish utilized both gill and skin mechanisms to similar degrees for HCO3- excretion, indicating that the gills are capable of excreting base equivalents. Hagfish exposed to chronic hypercapnia (48 h; 4% CO2) compensated for blood acidosis by mounting an ~70 mmol L-1 plasma [HCO3-] response. Upon reintroduction into normocapnic seawater, plasma [HCO3-] was rapidly corrected within 8 h. This correction occurred with impressive rates of plasma HCO3- loss (at peak: ~10 mmol kg-1 h-1) occurring primarily via carbonic anhydrase mediated CO2 offloading with only minor contributions from direct HCO3-/Cl- flux and insignificant contributions from increased glomerular filtration. During 48 h HEA (20 mmol L-1 [TAmm]; [total ammonia]) exposure, plasma [TAmm] increased 100-fold to over 5000 μmol L-1 while ammonia excretion (JAmm) was transiently inhibited. Plasma [TAmm] stabilized after 24–48 h exposure, possibly through lowering NH3 influx by reducing body NH3 permeability. Ammonia balance was subsequently maintained through the reestablishment of JAmm against inwardly directed ΔPNH3 and NH4+ electrochemical gradients. Restoration of JAmm by the hagfish during ammonia exposure likely involves secondary active transport of NH4+, possibly mediated by Na+/NH4+ (H+) exchange. Recovery from HEA in ammonia-free water was characterized by considerable ammonia washout, and restoration of plasma [TAmm] within 24 h. During recovery, JAmm occurred via branchial (70-80%) and cutaneous (20-30%) mechanisms. Excised hagfish skin fluxes revealed concentration-dependent (0.05 – 5 mmol L-1) JAmm with 8-fold greater JAmm across skin excised from HEA-exposed hagfish. Using immunohistochemical staining with a hagfish-specific Rhcg (ammonia/ammonium transporter) antibody, I demonstrated that Rhcg is present in cutaneous epidermal layers consistent with physiological data. Cutaneous O2 uptake by the hagfish has been previously suggested as the major site of systemic O2 acquisition. However, I show that hagfish rely primarily (85%) on branchial O2 uptake. When the branchial region was locally immersed in hypoxic conditions (4.6 kPa O2), hagfish did not utilize cutaneous mechanisms to acquire available O2 in the normoxic anterior chamber, suggesting that even when presented with restricted O2 availability, hagfish do not use cutaneous mechanisms to supplement metabolic O2 requirements. Using handling stress and mineral challenges (SO42- injections), I show that hagfish are capable of eliciting glucocorticoid and mineralocorticoid responses. Furthermore I show that these responses are not mediated by alterations in plasma cortisol, corticosterone, 11-deoxycorticosterone or 11-deoxycortisol. Overall in this thesis, I show that hagfish have developed novel cutaneous A/B and ammonia handling mechanisms along with extraordinary tolerances and effective recovery strategies to cope with exposure to extreme perturbations (e.g. hypercapnia, hypoxia, HEA). It is these strategies and mechanisms that allow this unique organism to survive and thrive in their demersal environment.

  • Subjects / Keywords
  • Graduation date
    2016-06:Fall 2016
  • Type of Item
  • Degree
    Doctor of Philosophy
  • DOI
  • License
    This thesis is made available by the University of Alberta Libraries with permission of the copyright owner solely for non-commercial purposes. This thesis, or any portion thereof, may not otherwise be copied or reproduced without the written consent of the copyright owner, except to the extent permitted by Canadian copyright law.
  • Language
  • Institution
    University of Alberta
  • Degree level
  • Department
    • Department of Biological Sciences
  • Specialization
    • Physiology, Cell and Developmental Biology
  • Supervisor / co-supervisor and their department(s)
    • Goss, Greg (Biological Sciences)
  • Examining committee members and their departments
    • Wright, Patrica (University of Guelph, Integrative Biology)
    • Gallin, Warren (Biological Sciences)
    • Young, James (Physiology)
    • Allison, Ted (Biological Sciences)