Suzanne C. Sukhdeo

EFFECTS OF CHOLINERGIC DRUGS ON LONGITUDINAL MUSCLE CONTRACTIONS OF FASCIOLA HEPATICA

Acetylcholine, cholinergic agonists and acetylcholinesterase inhibitors significantly decrease the amplitude and frequency of spontaneous longitudinal muscle contractions in Fasciola hepatica. In order of their effects on the inhibition of muscle contractions, the cholinergic agonists can be ranked as nicotine greater than carbachol greater than acetylcholine. High calcium ion concentration also causes a significant inhibition of contractions. Atropine, a cholinergic antagonist that acts on muscarinic receptors, significantly increases the amplitude and frequency of spontaneous contractions and completely reverses the effects of cholinomimetic drugs, including nicotine. In adult F. hepatica, the levels of acetylcholine and its precursor choline are 3.14 +/- 0.55 and 13.75 +/- 3.72 pmol/mg wet weight, respectively. The activities of choline acetyltransferase, specific acetylcholinesterase and the nonspecific cholinesterase are 1.25 +/- 0.19, 238.0 +/- 13.0, and 83.0 +/- 33.0 nmol/hr/mg protein, respectively.

Fixed behaviours and migration in parasitic flatworms

This paper considers how fixed behaviours may play a role in post-larval migrations of Entobdella soleae. A general argument is that a shift away from the paradigm of orientation is required to elucidate the mechanisms that parasites use to navigate on the surface of their hosts. Some migrations may rely on fixed behaviours (genetically programmed stereotyped behaviours) that often evolve under predictable environmental conditions with reliable signals. In turbulent and stochastic free-living environments, homeostatic hosts present very predictable topological substrates and physico-chemical characteristics to their parasites. Over the course of evolution on these predictable host substrates, adaptive behaviours in the parasites can become fixed. Examples of endoparasite migration behaviour, particularly that of the common liver fluke, Fasciola hepatica, will be used to develop an approach based on the perceptual worlds of migrating parasites. An important conclusion is that multi-disciplinary approaches, firmly rooted in an understanding of each parasites natural history, are requisite to successful interpretation of migration behaviours on the host.

Gastrointestinal hormones: environmental cues for Fasciola hepatica ?

The effects of pharmacological concentrations of several gastrointestinal hormones on the rate of sucker activity and the frequency and the amplitude of spontaneous longitudinal muscle contractions have been examined in adult Fasciola hepatica. Caerulein and serum decrease the rate of oral sucker activity; motilin decreases and CCK-PZ increases ventral sucker activity when compared to controls. Caerulein, serum and motilin significantly inhibit the frequency of contractions while bile, caerulein and motilin decrease the amplitude of contractions. These results suggest that F. hepatica can recognize and respond to certain gastrointestinal hormones and there may be adaptive value in these behavioural responses.

Immunohistochemical and electrochemical detection of serotonin in the nervous system of Fasciola hepatica, a parasitic flatworm.

The head region of the trematode parasite Fasciola hepatica contains 3.47 +/- 0.42 pmol/mg wet wt. of serotonin as measured by high-performance liquid chromatography coupled to electrochemical detection. The head region includes the cerebral ganglia, the transverse commissure and associated nervous tissue that innervates the musculature of the oral sucker, pharynx and body wall. Tissue from the tail, which contains little nervous innervation, has approximately 20 times less serotonin (0.18 +/- 0.01 pmol/mg wet wt.). Immunohistochemistry was used to identify serotonin-like immunoreactive cells. Bipolar and multipolar cell bodies in the cerebral ganglia show serotonin-like immunoreactivity. Also evident are serotonin-like immunoreactive processes in the neuropile and in the transverse commissure that connects the ganglia, and immunoreactive peripheral bipolar cell bodies innervating the musculature of the pharynx and body wall. The cell bodies containing serotonin are organized in bilateral symmetry with homologous cell bodies and processes represented in each ganglion and on both sides of the pharynx.

Site-Finding Behaviour of Fasciola Hepatica (Trematoda), a Parasitic Flatworm

Fasciola hepatica is a trematode parasite of the bile duct of herbivores. Site-finding behaviour of this parasite includes a migration from the duodenum through the abdominal cavity to the liver. This study examines the behaviour of the migrating worms at two stages of the life cycle; NEJ - the stage that penetrates the small intestine, and 48HR - the stage that penetrates the liver. Compared to saline controls, crude extracts of duodenal tissue have greater effects on the behaviour of the NEJs while crude extracts of liver tissue have greater effects on the behaviour of 48HRs. Yet, neither NEJs nor 48HRs migrate up gradients of liver extracts or down gradients of duodenal extracts. Stable chemical gradients are difficult to maintain in the motile abdominal cavity and it is suggested that orientation responses play no part in site-finding behaviour. We propose that the major component of site-finding behaviour of F. hepatica is a passive propulsion of the migrating stages through the viscera and along the body wall to the liver.

Histochemical localization of acetylcholinesterase in the cerebral ganglia of Fasciola hepatica, a parasitic flatworm

Acetylcholinesterase activity was found in the cell bodies and extracellularly in the neuropile of the cerebral ganglia of the adult trematode parasite, Fasciola hepatica. Within neuronal cell bodies of the cerebral ganglion, acetylcholinesterase reaction product was found in the endoplasmic reticulum, in the cisternae of the Golgi apparatus, and in secretory vesicles near the inner (releasing face) cisternae. Acetylcholinesterase reaction product was not seen intracellularly within any nerve processes. The reaction product was found around the somatic cell membranes and in the extracellular space between closely apposed nerve processes in the neuropile. Acetylcholinesterase reaction product was associated with synaptic endings that contained clear spheroidal synaptic vesicles, and the reaction product was localized at the site of synaptic contact between the zone of apposition of the pre- and postsynaptic terminals. This intracellular and extracellular distribution of the enzyme is consistent with its function as the degrading enzyme in cholinergic transmission.