Publications by authors named "Jeffrey R May"

The expansion of the target landscape of covalent inhibitors requires the engagement of nucleophiles beyond cysteine. Although the conserved catalytic lysine in protein kinases is an attractive candidate for a covalent approach, selectivity remains an obvious challenge. Moreover, few covalent inhibitors have been shown to engage the kinase catalytic lysine in animals.

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This investigation examined microRNA-208a (miR-208a) as a potential biomarker of isoproterenol (ISO)-induced cardiac injury in superoxide dismutase-2 (Sod2(+/-) ) and the wild-type mice, and the potential sensitivity of Sod2(+/-) mice to ISO-induced toxicity. A single intraperitoneal injection of ISO was administered to age-matched wild-type and Sod2(+/-) mice at 0, 80, or 160 mg/kg. Plasma miR-208a, cardiac troponin I (cTnI), and ISO systemic exposure were measured at various time points postdose.

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Article Synopsis
  • The study investigated the impact of dexamethasone alongside the gamma secretase inhibitor (GSI), PF-03084014, on goblet cell hyperplasia (GCH) in the intestines of Sprague-Dawley rats.
  • Two dosing regimens were analyzed: a pretreatment with dexamethasone followed by GSI, and concurrent intermittent treatment with both substances.
  • Results showed that dexamethasone reduced the severity of GCH temporarily, but there were safety concerns, including morbidity and mortality linked to high doses of GSI and dexamethasone coadministration.
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Female Tg rasH2 (CB6F1/Jic-TgrasH2@Tac) mice were administered water once daily, water twice daily with 8 or 12 hours between doses, 1% sodium dodecyl sulfate in water (1% SDS) once daily, or 1% SDS twice daily with 12 hours between doses by oral gavage at volumes of 10 ml/kg/day for 28 or 29 consecutive days. A control group of mice received no treatment and no sham manipulation. There were no significant differences in body weight or food consumption between treated groups and untreated control mice.

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While it is generally accepted that water hardness affects copper toxicity, the major ions that contribute to water hardness (calcium [Ca] and magnesium [Mg]) may affect copper toxicity differently. This is important because the Ca:Mg ratio in standard laboratory-reconstituted waters often differs from the ratio in natural surface waters. Copper toxicity was assessed for five different aquatic species: rainbow trout (RBT), fathead minnow (FHM), Ceriodaphnia dubia, Daphnia magna, and an amphipod (Gammarus sp.

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