Control of hemolymph volume by adjustments in urinary and drinking rates in the crab, cancer borealis

1986 ◽  
Vol 84 (4) ◽  
pp. 695-701 ◽  
Author(s):  
Timothy M Greco ◽  
Mitchell B Alden ◽  
Charles W Holliday
2021 ◽  
Vol 12 (4) ◽  
pp. 782-798
Author(s):  
Kellen DeLaney ◽  
Mengzhou Hu ◽  
Tessa Hellenbrand ◽  
Patsy S. Dickinson ◽  
Michael P. Nusbaum ◽  
...  

1990 ◽  
Vol 63 (1) ◽  
pp. 167-181 ◽  
Author(s):  
Warren Burggren ◽  
Alan Pinder ◽  
Brian McMahon ◽  
Michael Doyle ◽  
Michele Wheatly

1995 ◽  
Vol 354 (2) ◽  
pp. 282-294 ◽  
Author(s):  
Dawn M. Blitz ◽  
Andrew E. Christie ◽  
Eve Marder ◽  
Michael P. Nusbaum

2003 ◽  
Vol 308 (3) ◽  
pp. 535-544 ◽  
Author(s):  
Jurgen Huybrechts ◽  
Michael P Nusbaum ◽  
Luc Vanden Bosch ◽  
Geert Baggerman ◽  
Arnold De Loof ◽  
...  

1980 ◽  
Vol 88 (1) ◽  
pp. 147-160
Author(s):  
EVE MARDER ◽  
DANIÈLE PAUPARDIN-TRITSCH

A pharmacological analysis was made of the depolarizing acetylcholine (ACh) response found on the gastric mill 1 muscles of the crabs Cancer pagurus, Cancer irroratus and Cancer borealis. Acetylcholine, carbamylcholine, trimethylammonium, nicotine, and dimethyl-4-phenyl-piperazinium were effective in producing contractures and depolarizations in these muscles. No response to decamethonium, suberyldicholine, acetyl-β-methylcholine, carbamyl-β-methylcholine, pilocarpine and oxotremorine could be detected. High concentrations of muscarinic agonists (10−4 to 10−3 M) potentiated and prolonged the ACh iontophoretic response. When the acetylcholinesterase activity was inhibited with neostigmine, or when the response was elicited with carbamylcholine, muscarinic agonists partially inhibited the response. ACh responses were most effectively blocked by vertebrate nicotinic ganglionic antagonists, including dihydro-β-erythroidine, pempidine, and mecamylamine. α-Bungarotoxin was without effect on the ACh response.


1987 ◽  
Vol 252 (1) ◽  
pp. R153-R159 ◽  
Author(s):  
D. S. Miller ◽  
C. W. Holliday

In the crab, Cancer borealis, initial clearance studies showed a potent renal excretory system for the model organic cation, tetraethylammonium (TEA). TEA clearance averaged 145 +/- 32 ml/day, which was 18 times the paired polyethylene glycol clearance. TEA uptake by slices of urinary bladder was concentrative, saturable, inhibitable by N1-methylnicotinamide chloride, and dependent on glycolytic, but not oxidative, metabolism. When mounted in flux chambers, bladders exhibited a large net secretory flux. For 0.1 mM TEA, the ratio of secretory to reabsorptive fluxes was 65. Urinary bladders from another crab, Cancer irroratus, and a lobster, Homarus americanus, also exhibited net TEA secretion. In C. borealis bladder, secretory transport was concentrative, saturable, and nearly abolished by addition of 1 mM quinine to the serosal bath. Reabsorptive transport was not concentrative and was not reduced by luminal quinine. The data are consistent with a secretory pathway that is transcellular and mediated by carriers at both the serosal and luminal membranes.


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