Volume 15, Issue 3 (Fall 2011)
Physiol Pharmacol 2011, 15(3): 318-329 |
Back to browse issues page
Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:
Shahrokhi S S, Karami M, Kazemi B. Response to Morphine in a unicellular animal model (Paramecium caudatum). Physiol Pharmacol 2011; 15 (3) :318-329
URL: http://ppj.phypha.ir/article-1-715-en.html
URL: http://ppj.phypha.ir/article-1-715-en.html
Abstract: (13122 Views)
Introduction: Response to morphine and role of Nitric Oxide (NO) on expression of morphine response has been
studied in vertebrates. But, little evidence is provided in the matter in earlier invertebrates. This investigation for the
first time evaluated the effect of NO on expression of morphine potency in Paramecium caudatum.
Methods: Animal after isolation from natural media and specific identification was cultured in laboratory. 1 ml of
the isolated medium including the animals was added into the Sedgwick– Rafter cell counter. One μl of drugs was
infused into the cell counter. Morphine (1-60 μg/μl) was infused into the cell and its effect was recorded throughout 0-
180 sec. L-Arginine (1-8 μg/μl), a NO precursor, was infused prior to morphine (2 μg/μl). The NO producing enzyme
was inhibited by preinfusion of L-NAME. Also the naloxone was used to show the involvement of the opioid receptors
in the signaling of morphine response. In control speciements distilled water was added solely.
Results: The Paramecia under the infusion of morphine were aggregated. The most aggregation rate was observed
at a relatively low dose of the drug (2 μg/μl). L-Arginine showed a positive effect on the response (p<0.001) whearas
the effect was blocked by preinfusion of the L- NAME. Naloxone showed an inhibitory effect to morphine response.
The activity of the NOS was shown by using the NADPH-diaphorase.
Conclusion: A sign of morphine potency in single–celled animal is the cell aggregation, and the present results are
showing the interaction of NO system with the opioidergic system in this line. On the other hand, concerning the
potentiation effect of L-arginine on morphine effective dose in the model, this finding may be useful in reducing of
morphine’s side effects in patients under the treatment of the drug, and in the drug economy as well.
Type of Manuscript: Experimental research article |
Subject:
Pharmacokinetics/Dynamics
| Rights and permissions | |
 |
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. |
