Electroacupuncture alleviates spatial memory deficits in METH withdrawal mice by enhancing astrocyte-mediated glutamate clearance in the dCA1.

Methamphetamine (METH) elicits endogenous glutamate (Glu) in the brain, which could partially explain METH-induced memory deficits. Here, we investigated the therapeutic effects of electroacupuncture (EA) on spatial memory deficits in METH withdrawal mice and its potential synaptic mechanisms. We found that EA at acupoints 'Baihui' and 'Yintang' ameliorated the impaired spatial memory in METH withdrawal mice. In parallel, EA attenuated the Glu levels in vivo and suppressed the neuronal activities within dCA1 of METH withdrawal mice, as indicated by the decreasing c-Fos levels and the amplitude of mEPSP. In the dCA1, EA decreased A1-like astrocytes but increased astrocytic glutamatergic transporting molecules including glutamate transporter 1 and glutamine synthase. However, EA seemed to have no effects on presynaptic Glu transmission from the dCA3, as evidenced by the similiar levels of c-Fos in the dCA3 neurons, synaptic vesicular markers of dCA3 neural terminals and values of paired-pulse ratio in the dCA1 neurons between EA-treated and sham EA-treated METH withdrawal mice. These findings suggest that EA might normalize the dCA1 Glu levels at least in part through enhancing astrocyte-mediated Glu clearance. Taken together, astrocytes might be a novel target for developing therapeutic interventions against the impaired memory behaviours in METH users, and EA represents a promising non-invasive therapeutic strategy for the management of drug-caused memory deficits.

Converting evergreen broad-leaved forests into tea and Moso bamboo plantations affects labile carbon pools and the chemical composition of soil organic carbon.

This study aimed to explore the effects of conversion from evergreen broad-leaved forests (EBFs) to tea plantations (TPs) and Moso bamboo (Phyllostachys heterocycla var. pubescens) plantations (MBPs) and the subsequent long-term intensive management on the soil carbon pool and the chemical composition of soil organic carbon (SOC). Soil samples from three layers (0-10, 10-30 and 30-60 cm, respectively) were collected from adjacent EBFs, TPs and MBPs in An'ji County, Zhejiang Province, China. The physico-chemical properties of soils, including bulk density, SOC and its different fractions were determined. The chemical composition of SOC was also measured using 13C-nuclear magnetic resonance spectroscopy (NMR). The results showed that conversion from EBFs to TPs and MBPs decreased the concentrations of water soluble organic carbon (WSOC), light and heavy fraction organic carbon (LFOC, HFOC) and humus carbon (HC) (P < 0.05), reduced the O-alkyl C and carbonl C content, but increased the alkyl C, Aromatic C, aromaticity and the ratio of alkyl C/O-alkyl C (A/O-A) (P < 0.05). These results suggested that intensive management markedly altered the chemical structure of SOC and labile carbon pools. Our results demonstrated that converting EBFs to TPs and MBPs had a negative effect on SOC content and a positive effect on SOC stability. Therefore, management practices such as rational fertilization and sod cultivation are recommended after land-use conversion.

Effective cytotoxic activity of OSW-1 on colon cancer by inducing apoptosis in vitro and in vivo.

As a natural compound, Ornithogalum caudatum Ait is primarily used as an anti-inflammatory and antitumor agent in Chinese folk medicine. In 1992, OSW-1 was isolated from this compound, which is a new member of cholestane saponin family. In numerous recent studies, OSW-1 has been shown to have powerful cytotoxic anticancer effects against various malignant cells. However, the therapeutic efficacy of OSW-1 on colon cancer and the underlying mechanism are not understood. To explore the mechanism underlying OSW-1 in antitumor therapy, a therapeutic function analysis of OSW-1 on colon cancer was performed in vitro and in vivo. It was shown that with low toxicity on normal colonic cells, OSW-1 suppresses colon cancer cells in vitro and this inhibition was via the intrinsic apoptotic pathway, which increased cellular calcium, changed mitochondrial membrane potential, disrupted mitochondrial morphology, and led to the release of cytochrome c and the activation of caspase-3. Furthermore, in a nude mouse model, OSW-1 had a powerful effect on suppressing colon tumor proliferation without significant side effects through the apoptosis pathway. Taken together, these results demonstrate that OSW-1 is a potential drug for colon cancer treatment.