Literature DB >> 1499661

Effects of cocaine and its quaternary derivative cocaine methiodide on cardiovascular function in squirrel monkeys.

C W Schindler1, S R Tella, J L Katz, S R Goldberg.   

Abstract

The effects of cocaine and its quaternary derivative cocaine methiodide, which does not cross the blood-brain barrier, were studied on cardiovascular function in squirrel monkeys. In conscious monkeys, cocaine produced clear dose-dependent increases in blood pressure and heart rate, while cocaine methiodide did not. Both cocaine and cocaine methiodide enhanced the effects of norepinephrine in anesthetized animals, suggesting that both inhibit neuronal uptake of norepinephrine; cocaine was approximately 30 times more potent than cocaine methiodide. In anesthetized monkeys both cocaine and cocaine methiodide produced small, short duration pressor effects, although cocaine was at least 10 times more potent than cocaine methiodide. Cocaine's effects in anesthetized animals were clearly blunted in comparison to its effects in conscious animals. These effects of cocaine on blood pressure occurred at doses lower than those required to enhance norepinephrine's effects, indicating that the norepinephrine uptake blocking effects of the drugs cannot fully account for their cardiovascular effects. The greatly enhanced effect of cocaine in conscious animals and the finding that cocaine methiodide had little effect in conscious animals indicates that central mechanisms are involved in the effects of cocaine on cardiovascular function in conscious animals.

Entities:  

Mesh:

Substances:

Year:  1992        PMID: 1499661     DOI: 10.1016/0014-2999(92)90238-y

Source DB:  PubMed          Journal:  Eur J Pharmacol        ISSN: 0014-2999            Impact factor:   4.432


  7 in total

1.  Impaired cocaine-induced behavioral plasticity in the male offspring of cocaine-experienced sires.

Authors:  Mathieu E Wimmer; Fair M Vassoler; Samantha L White; Heath D Schmidt; Simone Sidoli; Yumiao Han; Benjamin A Garcia; R Christopher Pierce
Journal:  Eur J Neurosci       Date:  2019-01-06       Impact factor: 3.386

2.  Newly Developed Dopamine D3 Receptor Antagonists, R-VK4-40 and R-VK4-116, Do Not Potentiate Cardiovascular Effects of Cocaine or Oxycodone in Rats.

Authors:  Chloe J Jordan; Bree A Humburg; Eric B Thorndike; Anver Basha Shaik; Zheng-Xiong Xi; Michael H Baumann; Amy Hauck Newman; Charles W Schindler
Journal:  J Pharmacol Exp Ther       Date:  2019-09-27       Impact factor: 4.030

3.  Cocaine Exposure Increases Blood Pressure and Aortic Stiffness via the miR-30c-5p-Malic Enzyme 1-Reactive Oxygen Species Pathway.

Authors:  Wei Zhu; Huilan Wang; Jianqin Wei; Gregory C Sartor; Michelle Meiqi Bao; Clay T Pierce; Claes R Wahlestedt; Derek M Dykxhoorn; Chunming Dong
Journal:  Hypertension       Date:  2018-02-26       Impact factor: 10.190

4.  Nitric oxide as a mediator of cocaine-induced penile erection in the rat.

Authors:  J Y Chan; C L Huang; S H Chan
Journal:  Br J Pharmacol       Date:  1996-05       Impact factor: 8.739

5.  Cocaine engages a non-canonical, dopamine-independent, mechanism that controls neuronal excitability in the nucleus accumbens.

Authors:  Ilse Delint-Ramirez; Francisco Garcia-Oscos; Amir Segev; Saïd Kourrich
Journal:  Mol Psychiatry       Date:  2018-06-07       Impact factor: 15.992

6.  Delta Opioid Receptor Agonists Ameliorate Colonic Inflammation by Modulating Immune Responses.

Authors:  Kazuki Nagata; Hiroshi Nagase; Ayumi Okuzumi; Chiharu Nishiyama
Journal:  Front Immunol       Date:  2021-09-22       Impact factor: 7.561

7.  Potencies of cocaine methiodide on major cocaine targets in mice.

Authors:  Erik R Hill; Jinbin Tian; Michael R Tilley; Michael X Zhu; Howard H Gu
Journal:  PLoS One       Date:  2009-10-26       Impact factor: 3.240

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.