Paulina M Getsy, Gregory A Coffee, Santhosh M Baby, Walter J May, Fraser Henderson, Zackery T Knauss, Stephen J Lewis
{"title":"半胱甘氨酸-γ-裂解酶抑制剂dl -丙基甘氨酸增强l -半胱氨酸乙酯克服吗啡对呼吸的不良影响的能力。","authors":"Paulina M Getsy, Gregory A Coffee, Santhosh M Baby, Walter J May, Fraser Henderson, Zackery T Knauss, Stephen J Lewis","doi":"10.1152/ajplung.00003.2025","DOIUrl":null,"url":null,"abstract":"<p><p>l-cysteine ethyl ester (l-CYSee) overcomes adverse effects elicited by systemic injection of morphine on ventilatory parameters and arterial blood-gas chemistry in rats. l-CYSee or l-cysteine, resulting from the deesterification of l-CYSee, may enter enzymatic cascades that produce the ventilatory stimulant molecule, hydrogen sulfide (H<sub>2</sub>S). dl-propargylglycine (dl-PROP) is an inhibitor of cystathionine-γ-lyase (CSE)-mediated conversion of l-cysteine to H<sub>2</sub>S and has been widely used <i>in vivo</i>. We examined whether l-CYSee (2 injections × 500 µmol/kg, IV)-induced reversal of the changes in ventilation elicited by morphine (10 mg/kg, IV) in freely moving male Sprague Dawley rats was altered by prior administration of dl-PROP (25 mg/kg, IV). The major findings were <i>1</i>) the effects of morphine on ventilatory parameters were not affected by subsequent injection of dl-PROP; <i>2</i>) first injection of l-CYSee elicited a prompt reversal of the adverse effects of morphine that was more pronounced in dl-PROP-treated than vehicle-treated rats; and <i>3</i>) the actions of the second injection of l-CYSee were dramatically augmented in dl-PROP-treated rats. In addition, the changes in many of the ventilatory parameters during a subsequent hypoxic-hypercapnic (HH) gas challenge were augmented substantially by dl-PROP. This study demonstrates that <i>1</i>) inhibition of CSE with dl-PROP does not affect the ventilatory actions of morphine, <i>2</i>) reversal effects of l-CYSee were augmented by blockade of CSE, and <i>3</i>) blockade of CSE augments the ventilatory responses to HH gas challenge in morphine-treated rats. These unexpected findings suggest that the CSE-dependent production of H<sub>2</sub>S from l-CYSee countermands l-CYSee reversal of morphine-induced respiratory depression in rats.<b>NEW & NOTEWORTHY</b> The ability of l-cysteine ethyl ester (l-CYSee) to overcome the adverse effects of morphine on breathing is exaggerated by inhibition of cystathionine-γ-lyase (CSE), suggesting that conversion of l-CYSee or l-cysteine to H<sub>2</sub>S countermands the effects of l-CYSee against morphine.</p>","PeriodicalId":7593,"journal":{"name":"American journal of physiology. Lung cellular and molecular physiology","volume":" ","pages":"L809-L825"},"PeriodicalIF":3.5000,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12199168/pdf/","citationCount":"0","resultStr":"{\"title\":\"The cystathionine-γ-lyase inhibitor DL-propargylglycine augments the ability of L-cysteine ethyl ester to overcome the adverse effects of morphine on breathing.\",\"authors\":\"Paulina M Getsy, Gregory A Coffee, Santhosh M Baby, Walter J May, Fraser Henderson, Zackery T Knauss, Stephen J Lewis\",\"doi\":\"10.1152/ajplung.00003.2025\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>l-cysteine ethyl ester (l-CYSee) overcomes adverse effects elicited by systemic injection of morphine on ventilatory parameters and arterial blood-gas chemistry in rats. l-CYSee or l-cysteine, resulting from the deesterification of l-CYSee, may enter enzymatic cascades that produce the ventilatory stimulant molecule, hydrogen sulfide (H<sub>2</sub>S). dl-propargylglycine (dl-PROP) is an inhibitor of cystathionine-γ-lyase (CSE)-mediated conversion of l-cysteine to H<sub>2</sub>S and has been widely used <i>in vivo</i>. We examined whether l-CYSee (2 injections × 500 µmol/kg, IV)-induced reversal of the changes in ventilation elicited by morphine (10 mg/kg, IV) in freely moving male Sprague Dawley rats was altered by prior administration of dl-PROP (25 mg/kg, IV). The major findings were <i>1</i>) the effects of morphine on ventilatory parameters were not affected by subsequent injection of dl-PROP; <i>2</i>) first injection of l-CYSee elicited a prompt reversal of the adverse effects of morphine that was more pronounced in dl-PROP-treated than vehicle-treated rats; and <i>3</i>) the actions of the second injection of l-CYSee were dramatically augmented in dl-PROP-treated rats. In addition, the changes in many of the ventilatory parameters during a subsequent hypoxic-hypercapnic (HH) gas challenge were augmented substantially by dl-PROP. This study demonstrates that <i>1</i>) inhibition of CSE with dl-PROP does not affect the ventilatory actions of morphine, <i>2</i>) reversal effects of l-CYSee were augmented by blockade of CSE, and <i>3</i>) blockade of CSE augments the ventilatory responses to HH gas challenge in morphine-treated rats. These unexpected findings suggest that the CSE-dependent production of H<sub>2</sub>S from l-CYSee countermands l-CYSee reversal of morphine-induced respiratory depression in rats.<b>NEW & NOTEWORTHY</b> The ability of l-cysteine ethyl ester (l-CYSee) to overcome the adverse effects of morphine on breathing is exaggerated by inhibition of cystathionine-γ-lyase (CSE), suggesting that conversion of l-CYSee or l-cysteine to H<sub>2</sub>S countermands the effects of l-CYSee against morphine.</p>\",\"PeriodicalId\":7593,\"journal\":{\"name\":\"American journal of physiology. 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The cystathionine-γ-lyase inhibitor DL-propargylglycine augments the ability of L-cysteine ethyl ester to overcome the adverse effects of morphine on breathing.
l-cysteine ethyl ester (l-CYSee) overcomes adverse effects elicited by systemic injection of morphine on ventilatory parameters and arterial blood-gas chemistry in rats. l-CYSee or l-cysteine, resulting from the deesterification of l-CYSee, may enter enzymatic cascades that produce the ventilatory stimulant molecule, hydrogen sulfide (H2S). dl-propargylglycine (dl-PROP) is an inhibitor of cystathionine-γ-lyase (CSE)-mediated conversion of l-cysteine to H2S and has been widely used in vivo. We examined whether l-CYSee (2 injections × 500 µmol/kg, IV)-induced reversal of the changes in ventilation elicited by morphine (10 mg/kg, IV) in freely moving male Sprague Dawley rats was altered by prior administration of dl-PROP (25 mg/kg, IV). The major findings were 1) the effects of morphine on ventilatory parameters were not affected by subsequent injection of dl-PROP; 2) first injection of l-CYSee elicited a prompt reversal of the adverse effects of morphine that was more pronounced in dl-PROP-treated than vehicle-treated rats; and 3) the actions of the second injection of l-CYSee were dramatically augmented in dl-PROP-treated rats. In addition, the changes in many of the ventilatory parameters during a subsequent hypoxic-hypercapnic (HH) gas challenge were augmented substantially by dl-PROP. This study demonstrates that 1) inhibition of CSE with dl-PROP does not affect the ventilatory actions of morphine, 2) reversal effects of l-CYSee were augmented by blockade of CSE, and 3) blockade of CSE augments the ventilatory responses to HH gas challenge in morphine-treated rats. These unexpected findings suggest that the CSE-dependent production of H2S from l-CYSee countermands l-CYSee reversal of morphine-induced respiratory depression in rats.NEW & NOTEWORTHY The ability of l-cysteine ethyl ester (l-CYSee) to overcome the adverse effects of morphine on breathing is exaggerated by inhibition of cystathionine-γ-lyase (CSE), suggesting that conversion of l-CYSee or l-cysteine to H2S countermands the effects of l-CYSee against morphine.
期刊介绍:
The American Journal of Physiology-Lung Cellular and Molecular Physiology publishes original research covering the broad scope of molecular, cellular, and integrative aspects of normal and abnormal function of cells and components of the respiratory system. Areas of interest include conducting airways, pulmonary circulation, lung endothelial and epithelial cells, the pleura, neuroendocrine and immunologic cells in the lung, neural cells involved in control of breathing, and cells of the diaphragm and thoracic muscles. The processes to be covered in the Journal include gas-exchange, metabolic control at the cellular level, intracellular signaling, gene expression, genomics, macromolecules and their turnover, cell-cell and cell-matrix interactions, cell motility, secretory mechanisms, membrane function, surfactant, matrix components, mucus and lining materials, lung defenses, macrophage function, transport of salt, water and protein, development and differentiation of the respiratory system, and response to the environment.