Current treatments for neuropathic pain are suboptimal,necessitating the search for more effective therapeutics.Our previous study showed that inhibition of neuroinflammation in the spinal cord induced analgesic effec...Current treatments for neuropathic pain are suboptimal,necessitating the search for more effective therapeutics.Our previous study showed that inhibition of neuroinflammation in the spinal cord induced analgesic effects,and focal repetitive trans-spinal magnetic stimulation showed an anti-neuroinflammatory effect in spinal cord injury rat models.Here,we speculated that repetitive trans-spinal magnetic stimulation might induce an anti-inflammatory effect to alleviate neuropathic pain by upregulating calmodulin-dependent protein kinase kinase beta(CaMKKβ)/adenosine 5′-monophosphate-activated protein kinase(AMPK)/suppressor of cytokine signaling-3(SOCS3)signaling in microglia.Experiments have found that non-invasive focal repetitive trans-spinal magnetic stimulation effectively alleviates mechanical allodynia and spinal neuroinflammation in rats with neuropathic pain induced by chronic sciatic nerve ligation.Further research found that repetitive trans-spinal magnetic stimulation upregulated the expression of SOCS3 in spinal microglia,which subsequently inhibited the phosphorylation of p38 mitogen-activated protein kinase and signal transducer and activator of transcription 3 and nuclear factor-kappa B p65 nuclear translocation in rats with neuropathic pain,thereby suppressing neuroinflammation.The upregulation of SOCS3 by repetitive trans-spinal magnetic stimulation may be achieved through the activation of the CaMKKβ/AMPK signaling pathway in microglia.The results suggested that focal repetitive trans-spinal magnetic stimulation inhibits spinal neuroinflammation and alleviates neuropathic pain by activating the CaMKKβ/AMPK/SOCS3 signaling pathway in spinal microglia.This mechanism provides an effective noninvasive treatment for neuropathic pain caused by peripheral nerve injury.展开更多
The asymmetric reduction of carbonyl compounds by means of the Ru-chiral diphosphine-chiral diamine catalysts is widely useful in organic synthesis where high levels of enantioselectivities have been attributed to mul...The asymmetric reduction of carbonyl compounds by means of the Ru-chiral diphosphine-chiral diamine catalysts is widely useful in organic synthesis where high levels of enantioselectivities have been attributed to multiple ligand chiral elements as well as essential stereochemical matching synergies within them.Described here is the design and discovery of new pincer-type Ru-catalysts that feature only single stereogenic element within ligands,yet the such significantly simplified structure is demonstrated to be well competent for effecting asymmetric reductions as well as kinetic resolutions over a broad range of highly functionalized ketones/alcohols,including heteroaryl substituted substrates that were challenging by known catalyst systems.Alcohols were furnished not only in excellent enantioselectivities,but with turnover numbers(up to 100,000 TONs)that reach the highest levels known to date in asymmetric transfer hydrogenation of ketones.This work should help shed light on the intricate origin of enantioselection in these important processes,and further stimulate rational understanding as well as optimization of chiral catalysts towards efficiency and simplicity.展开更多
基金National Natural Science Foundation of China,Nos.82302877(to QW),82172541(to TW)the Natural Science Foundation of Hunan Province,No.2023JJ30549(to QW)Clinical Medical Technology Innovation Guidance Project of Hunan Provincial Science and Technology Department,No.2021SK51815(to QW).
文摘Current treatments for neuropathic pain are suboptimal,necessitating the search for more effective therapeutics.Our previous study showed that inhibition of neuroinflammation in the spinal cord induced analgesic effects,and focal repetitive trans-spinal magnetic stimulation showed an anti-neuroinflammatory effect in spinal cord injury rat models.Here,we speculated that repetitive trans-spinal magnetic stimulation might induce an anti-inflammatory effect to alleviate neuropathic pain by upregulating calmodulin-dependent protein kinase kinase beta(CaMKKβ)/adenosine 5′-monophosphate-activated protein kinase(AMPK)/suppressor of cytokine signaling-3(SOCS3)signaling in microglia.Experiments have found that non-invasive focal repetitive trans-spinal magnetic stimulation effectively alleviates mechanical allodynia and spinal neuroinflammation in rats with neuropathic pain induced by chronic sciatic nerve ligation.Further research found that repetitive trans-spinal magnetic stimulation upregulated the expression of SOCS3 in spinal microglia,which subsequently inhibited the phosphorylation of p38 mitogen-activated protein kinase and signal transducer and activator of transcription 3 and nuclear factor-kappa B p65 nuclear translocation in rats with neuropathic pain,thereby suppressing neuroinflammation.The upregulation of SOCS3 by repetitive trans-spinal magnetic stimulation may be achieved through the activation of the CaMKKβ/AMPK signaling pathway in microglia.The results suggested that focal repetitive trans-spinal magnetic stimulation inhibits spinal neuroinflammation and alleviates neuropathic pain by activating the CaMKKβ/AMPK/SOCS3 signaling pathway in spinal microglia.This mechanism provides an effective noninvasive treatment for neuropathic pain caused by peripheral nerve injury.
基金supported by Shenzhen Nobel Prize Scientists Laboratory Project(C17783101)Shenzhen YOUWEI Tech Group,Guangdong Provincial Key Laboratory of Catalysis(2020B121201002)+2 种基金the Natural Science Foundation of Guangdong Province(2021A1515010329)the National Natural Science Foundation of China(22171128)Shenzhen Science and Technology Program(KQTD20180411143514543,JCYJ20190809143611743)。
文摘The asymmetric reduction of carbonyl compounds by means of the Ru-chiral diphosphine-chiral diamine catalysts is widely useful in organic synthesis where high levels of enantioselectivities have been attributed to multiple ligand chiral elements as well as essential stereochemical matching synergies within them.Described here is the design and discovery of new pincer-type Ru-catalysts that feature only single stereogenic element within ligands,yet the such significantly simplified structure is demonstrated to be well competent for effecting asymmetric reductions as well as kinetic resolutions over a broad range of highly functionalized ketones/alcohols,including heteroaryl substituted substrates that were challenging by known catalyst systems.Alcohols were furnished not only in excellent enantioselectivities,but with turnover numbers(up to 100,000 TONs)that reach the highest levels known to date in asymmetric transfer hydrogenation of ketones.This work should help shed light on the intricate origin of enantioselection in these important processes,and further stimulate rational understanding as well as optimization of chiral catalysts towards efficiency and simplicity.
