Key result
Small molecule AT2R antagonists, particularly EMA400 and EMA401, demonstrated higher oral bioavailability (~30%) and dose-dependent pain relief in a rat model of neuropathic pain.
Why the study?
Do small molecule AT2R antagonists demonstrate favorable pharmacokinetics and provide pain relief in a rat model of neuropathic pain?
Do small molecule AT2R antagonists demonstrate favorable pharmacokinetics and provide pain relief in a rat model of neuropathic pain?
Small molecule AT2R antagonists, particularly EMA400 and EMA401, demonstrate favorable oral bioavailability and dose-dependent pain relief in a rat model of neuropathic pain.
Hypothesis-generating for AT2R antagonists in neuropathic pain; human trials required before any clinical consideration.
OBJECTIVE: Neuropathic pain is an area of unmet clinical need. The objective of this study was to define the pharmacokinetics, oral bioavailability, and efficacy in rats of small molecule antagonists of the angiotensin II type 2 receptor (AT₂R) for the relief of neuropathic pain. DESIGN AND METHODS: Adult male Sprague-Dawley (SD) rats received single intravenous (1-10 mg/kg) or oral (5-10 mg/kg) bolus doses of EMA200, EMA300, EMA400 or EMA401 (S-enantiomer of EMA400). Blood samples were collected immediately pre-dose and at specified times over a 12- to 24-hour post-dosing period. Liquid chromatography tandem mass spectrometry was used to measure plasma drug concentrations. Efficacy was assessed in adult male SD rats with a unilateral chronic constriction injury (CCI) of the sciatic nerve. RESULTS: After intravenous administration in rats, mean (±standard error of the mean) plasma clearance for EMA200, EMA300, EMA400, and EMA401 was 9.3, 6.1, 0.7, and 1.1 L/hour/kg, respectively. After oral dosing, the dose-normalized systemic exposures of EMA400 and EMA401 were 20- to 30-fold and 50- to 60-fold higher than that for EMA300 and EMA200, respectively. The oral bioavailability of EMA400 and EMA401 was similar at ∼30%, whereas it was only 5.9% and 7.1% for EMA200 and EMA300, respectively. In CCI rats, single intraperitoneal bolus doses of EMA200, EMA300, and EMA400 evoked dose-dependent pain relief. The pain relief potency rank order in CCI rats was EMA400 > EMA300 > EMA200 in agreement with the dose-normalized systemic exposure rank order in SD rats. CONCLUSION: The small molecule AT₂R antagonist, EMA401, is in clinical development as a novel analgesic for the relief of neuropathic pain.
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Smith et al. (2013) studied Neuropathic pain. EMA200, EMA300, EMA400, and EMA401 (AT2R antagonists) was evaluated on Pharmacokinetics (plasma clearance, oral bioavailability) and pain relief. Small molecule AT2R antagonists, particularly EMA400 and EMA401, demonstrated higher oral bioavailability (~30%) and dose-dependent pain relief in a rat model of neuropathic pain.
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