spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    

This Article
Right arrow Full Text (PDF)
Right arrow References
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Wilkens, J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Wilkens, J.

Journal of Experimental Biology, Vol 200, Issue 3 487-493, Copyright © 1997 by Company of Biologists


JOURNAL ARTICLES

Possible mechanisms of control of vascular resistance in the lobster Homarus americanus

J Wilkens

In Homarus americanus, the resistance to fluid flow through each of the arteries leaving the heart, including the complete hemocoelic return pathways, can be controlled. Each of the five arterial types (anterior median, paired anterior lateral, paired hepatic, sternal and dorsal abdominal) exhibits a unique spectrum of responses to a battery of neurotransmitters (acetylcholine, glutamic acid, -aminobutyric acid) and neurohormones (dopamine, octopamine, 5-hydroxytryptamine, crustacean cardioactive peptide, FLRFamide-related peptides F1 and F2, and proctolin). Acetylcholine causes increases in resistance in all arteries except the anterior median artery; in the dorsal abdominal artery, this increase is antagonized by -aminobutyric acid. All neurohormones that are effective in a particular artery cause increases in resistance to flow. The sites of action of these compounds in the dorsal abdominal artery are valves located at major branch points; the sites of control in the other arteries are not known. It is concluded that the control of arterial resistance is a mechanism which the animal can exploit to produce different flow patterns among the various arteries.


This article has been cited by other articles:


Home page
J. Exp. Biol.Home page
G. Maurer, J. L. Wilkens, and M. K. Grieshaber
Modulatory effects of adenosine and adenine nucleotides on different heart preparations of the American lobster, Homarus americanus
J. Exp. Biol., March 1, 2008; 211(5): 661 - 670.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
J. L. Wilkens, M. J. Cavey, I. Shovkivska, M. L. Zhang, and H. E. D. J. t. Keurs
Elasticity, unexpected contractility and the identification of actin and myosin in lobster arteries
J. Exp. Biol., March 1, 2008; 211(5): 766 - 772.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
J. A. Guadagnoli, K. Tobita, and C. L. Reiber
Assessment of the pressure-volume relationship of the single ventricle of the grass shrimp, Palaemonetes pugio
J. Exp. Biol., June 15, 2007; 210(12): 2192 - 2198.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
A. J. King, S. M. Henderson, M. H. Schmidt, A. G. Cole, and S. A. Adamo
Using ultrasound to understand vascular and mantle contributions to venous return in the cephalopod Sepia officinalis L.
J. Exp. Biol., June 1, 2005; 208(11): 2071 - 2082.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
H. H. Taylor and P. Greenaway
Osmoregulation in the terrestrial Christmas Island red crab Gecarcoidea natalis (Brachyura: Gecarcinidae): modulation of branchial chloride uptake from the urine
J. Exp. Biol., October 15, 2002; 205(20): 3251 - 3260.
[Abstract] [Full Text] [PDF]




© The Company of Biologists Ltd 1997