Whole body autoradiography and microautoradiography in eels after intra-arterial administration of 125I-labeled eel ANP

1996 ◽  
Vol 271 (4) ◽  
pp. R926-R935 ◽  
Author(s):  
H. Sakaguchi ◽  
H. Suzuki ◽  
H. Hagiwara ◽  
H. Kaiya ◽  
Y. Takei ◽  
...  

125I-labeled eel atrial natriuretic peptide (ANP) was administered into the ventral or dorsal aorta of freshwater (FW) and seawater (SW) eels, Anguilla japonica, and the major target organs were explored by whole body autoradiography. Localization of the ANP binding in the target organs was also examined at tissue and cell levels by microautoradiography using tissue sections. Whole body autoradiography revealed that the specific label was accumulated predominantly in the gill, with lesser amounts in the atrium, kidney, liver, and urinary bladder. Autoradiographic grains were most dense in the secondary lamellae of the gill, particularly on the side of the efferent filamental artery. Other binding sites in target tissues were the glomerulus of the kidney, epicardium and endocardium of the atrium, bile duct/blood vessels of the liver, and interrenal cells of the head kidney. There was no difference in the distribution and density of grains between injections into the ventral aorta and dorsal aorta, although, in the former, injected 125I-labeled eel ANP passes through the gill before reaching peripheral target tissues. There was a tendency for downregulation of ANP binding sites in SW eels, especially in the gill. These results show that specific ANP binding sites are present in organs that are implicated in osmoregulation and cardiovascular regulation in eels and further suggest that the number of ANP binding sites varies according to changes in the environmental salinity.

2008 ◽  
Vol 43 (4) ◽  
pp. 265-274 ◽  
Author(s):  
Claude Rouleau ◽  
Jagmohan Kohli

Abstract Nonpersistent contaminants represent thousands of chemicals used as pesticides, pharmaceuticals, personal care products, additives, etc. Because of this diversity, the assessment of the environmental risks they may pose for the environment represents a formidable task. Identification of target organs is key information needed to orient further research on newlyinvestigated organic xenobiotics. We used whole-body autoradiography to visualize the distribution of 14C-labelled atrazine, methoxychlor, glyphosate, and bisphenol-A in goldfish (Carassius auratus) and identify target organs. Fish were exposed for 2 days (glyphosate and bisphenol-A) and 7 days (atrazine and methoxychlor) to the radiolabelled compounds at a concentration of 15 nM. They were then frozen, embedded in carboxymethylcellulose gel, 20-μm-thick cryosections were collected, freeze-dried, and exposed to phosphor screens to visualize the tissue distribution of radioactivity. Goldfish did not accumulate glyphosate. The three other compounds were accumulated, mostly in the gall bladder. Nevertheless, unforeseen accumulation sites were observed; atrazine accumulated in the uveal tract of the eye, high levels of radioactivity were found in the cerebrospinal fluid of goldfish exposed to methoxychlor, and an important accumulation of bisphenol-A was seen in urine, oral mucosa, esophagus, and intestinal lumen. The potential toxicological consequences of the accumulation of these chemicals at very specific locations within the fish body are discussed and further research suggested.


1985 ◽  
Vol 18 (3) ◽  
pp. 305-312 ◽  
Author(s):  
HIDEYUKI GOTO ◽  
MASAAKI MATSUSHIMA ◽  
TOSHIYUKI MARUYAMA ◽  
TAKASHI KIHARA

Author(s):  
Burton B. Silver ◽  
Ronald S. Nelson

Some investigators feel that insulin does not enter cells but exerts its influence in some manner on the cell surface. Ferritin labeling of insulin and insulin antibody was used to determine if binding sites of insulin to specific target organs could be seen with electron microscopy.Alloxanized rats were considered diabetic if blood sugar levels were in excess of 300 mg %. Test reagents included ferritin, ferritin labeled insulin, and ferritin labeled insulin antibody. Target organs examined were were diaphragm, kidney, gastrocnemius, fat pad, liver and anterior pituitary. Reagents were administered through the left common carotid. Survival time was at least one hour in test animals. Tissue incubation studies were also done in normal as well as diabetic rats. Specimens were fixed in gluteraldehyde and osmium followed by staining with lead and uranium salts. Some tissues were not stained.


1980 ◽  
Vol 13 (2) ◽  
pp. 202-210 ◽  
Author(s):  
MASAHITO WATANABE ◽  
TAKASHI KIHARA ◽  
MASAHISA SHIMADA ◽  
KIYOHISA KURIMOTO

1979 ◽  
Vol 83 (1) ◽  
pp. 31-39 ◽  
Author(s):  
JOHN H. BOOTH

Injecting vitally stained blood cells into the ventral aorta of unrestrained, cannulated fish, and rapid freezing in liquid nitrogen, permitted the examination of the effects of oxygen supply, epinephrine and acetylcholine on branchial lamellar perfusion. Compared to the conditions in resting fish in air-saturated water, hypoxia and injection of epinephrine significantly increased the proportion of secondary lamellae receiving stained cells, and acetylcholine caused a significant reduction, but hyperoxia did not significantly affect the proportion of lamellae containing stained cells. Perfusion of the filamental central compartment was not affected by the treatments. It is concluded that trout can respond to changes in oxygen supply by varying the number of secondary lamellae perfused with blood, and that the distribution of blood flow is regulated by cholinergic and adrenergic receptors. It is suggested, however, that lamellar recruitment would not be useful in minimizing the costs of osmo- and iono-regulation.


2016 ◽  
Vol 2016 ◽  
pp. 1-9
Author(s):  
Xiaoli Shen ◽  
Lina Huang ◽  
Dahui Ma ◽  
Jun Zhao ◽  
Yi Xie ◽  
...  

Ultrasound microbubble combined optic protection drugs have obvious protective effect on optic nerve damage. This way of targeting drug delivery is becoming more simple, not through the whole body metabolism, avoiding drug via blood circulation when facing the decomposition and the environment in the interference and destruction process of drugs, to maximize the guarantee to reach target organs of drug concentration and to reache the maximum therapeutic effect. The technique of ultrasound microbubbles is safe, controllable, nonimmunogenic, and repeatable. It provides us with a novel idea in the administration of neuroprotective drugs.


Sign in / Sign up

Export Citation Format

Share Document