D-cysteine ethyl ester and D-cystine dimethyl ester reverse the deleterious effects of morphine on arterial blood-gas chemistry and Alveolar-arterial gradient in anesthetized rats

• Published in: Respiratory physiology & neurobiology Vol. 302; p. 103912
• Main Authors: Getsy, Paulina M., Young, Alex P., Grossfield, Alan, Seckler, James M., Wilson, Christopher G., Gaston, Benjamin, Bates, James N., Lewis, Stephen J.
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 01.08.2022
• Subjects: Anesthetized rats; Animals; Arterial blood gases; Cysteine - analogs & derivatives; Cysteine - pharmacology; Cystine - analogs & derivatives; Cystine - pharmacology; D-cysteine ethyl ester; D-cystine dimethyl ester; Morphine; Morphine - pharmacology; Rats; Rats, Sprague-Dawley; Anesthetized rats; Morphine; D-cystine dimethyl ester; Arterial blood gases; D-cysteine ethyl ester
• ISSN: 1569-9048; 1878-1519
• DOI: 10.1016/j.resp.2022.103912

We determined whether intravenous injections of the membrane-permeable ventilatory stimulants, D-cysteine ethyl ester (ethyl (2 S)− 2-amino-3-sulfanylpropanoate) (D-CYSee) and D-cystine dimethyl ester (methyl (2 S)− 2-amino-3-[[(2 S)− 2-amino-3-methoxy-3-oxopropyl]disulfanyl] propanoate) (D-CYSdime), could overcome the deleterious actions of intravenous morphine on arterial blood pH, pCO2, pO2 and sO2, and Alveolar-arterial (A-a) gradient (i.e., the measure of exchange of gases in the lungs) in Sprague Dawley rats anesthetized with isoflurane. Injection of morphine (2 mg/kg, IV) caused pronounced reductions in pH, pO2 and sO2 accompanied by elevations in pCO2, all which are suggestive of diminished ventilation, and elevations in A-a gradient, which suggests a mismatch of ventilation-perfusion. Subsequent boluses of D-cysteine ethyl ester (2 ×100 μmol/kg, IV) or D-cystine dimethyl ester (2 ×50 μmol/kg, IV) rapidly reversed of the negative actions of morphine on pH, pCO2, pO2 and sO2, and A-a gradient. Similar injections of D-cysteine (2 ×100 μmol/kg, IV) were without effect, whereas injections of D-cystine (2 ×50 μmol/kg, IV) produced a modest reversal. Our data show that D-cysteine ethyl ester and D-cystine dimethyl ester readily overcome the deleterious effects of morphine on arterial blood gas (ABG) chemistry and A-a gradient by mechanisms that may depend upon their ability to rapidly enter cells. As a result of their known ability to enter the brain, lungs, muscles of the chest wall, and most likely the major peripheral chemoreceptors (i.e., carotid bodies), the effects of the thiolesters on changes in ABG chemistry and A-a gradient elicited by morphine likely involve central and peripheral mechanisms. We are employing target prediction methods to identify an array of in vitro and in vivo methods to test potential functional proteins by which D-CYSee and D-CYSdime modulate the effects of morphine on breathing. •D-cysteine ethyl ester reversed morphine’s effects on arterial blood gas chemistry.•D-cysteine did not overcome the effects of morphine on arterial blood gas chemistry.•The effects of thiolesters may involve rapid entry into respiratory control cells.