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1.
Bioresour Technol ; 376: 128856, 2023 May.
Article En | MEDLINE | ID: mdl-36907227

Enhancing the degradation of lignocellulosic structure is essential for the efficient use of corn stover. This study investigated the effects of using urea combined with steam explosion on the enzymatic hydrolysis and ethanol production of corn stover. The results demonstrated that 4.87% urea addition and 1.22 MPa steam pressure were optimal for ethanol production. The highest reducing sugar yield (350.12 mg/g) was increased by 116.42% (p < 0.05), and the corresponding degradation rates of cellulose, hemicellulose, and lignin in pretreated corn stover were increased by 40.26%, 45.89% and 53.71% compared with the untreated corn stover (p < 0.05). Moreover, the maximal sugar alcohol conversion rate was approximately 48.3%, and the ethanol yield reached 66.5%. In addition, the key functional groups in corn stover lignin under combined pretreatment were identified. These findings offer new insights into corn stover pretreatment and can help develop feasible technologies to enhance ethanol production.


Lignin , Steam , Lignin/chemistry , Zea mays/metabolism , Ethanol/metabolism , Cellulose/metabolism , Hydrolysis
2.
Bioresour Technol ; 377: 128845, 2023 Jun.
Article En | MEDLINE | ID: mdl-36898564

Investigating the effect of butyric acid concentration on anaerobic digestion systems in complex systems is important for the efficient degradation of butyric acid and improving the efficiency of anaerobic digestion. In this study, different loadings of butyric acid with 2.8, 3.2, and 3.6 g/(L·d) were added to the anaerobic reactor. At a high organic loading rate of 3.6 g/(L·d), methane was efficiently produced with VBP (Volumetric Biogas Production) of 1.50 L/(L·d) and biogas content between 65% and 75%. VFAs concentration remained below 2000 mg/L. Metagenome sequencing revealed changes in the functional flora within different stages. Methanosarcina, Syntrophomonas, and Lentimicrobium were the main and functional microorganisms. That the relative abundance of methanogens exceeded 35% and methanogenic metabolic pathways were increased indicated the methanogenic capacity of the system significantly improved. The presence of a large number of hydrolytic acid-producing bacteria also indicated the importance of the hydrolytic acid-producing stage in the system.


Euryarchaeota , Microbiota , Anaerobiosis , Butyric Acid , Biofuels , Bioreactors/microbiology , Euryarchaeota/metabolism , Metabolic Networks and Pathways , Methane
3.
J Biochem Mol Toxicol ; 31(6)2017 Jun.
Article En | MEDLINE | ID: mdl-28186389

Corticosterone plays an important role in feeding behavior. However, its mechanism remains unclear. Therefore, the present study aimed to investigate the effect of corticosterone on feeding behavior. In this study, cumulative food intake was increased by acute corticosterone administration in a dose-dependent manner. Administration of the 5-HT2c receptor agonist m-chlorophenylpiperazin (mCPP) reversed the effect of corticosterone on food intake. The anorectic effects of mCPP were also blocked by the 5-HT2c receptor antagonist RS102221 in corticosterone-treated mice. Both corticosterone and mCPP increased c-Fos expression in hypothalamic nuclei, but not the nucleus of the solitary tract. RS102221 inhibited c-Fos expression induced by mCPP, but not corticosterone. In addition, mCPP had little effect on TH and POMC levels in the hypothalamus. Furthermore, mCPP antagonized decreasing effect of the leptin produced by corticosterone. Taken together, our findings suggest that 5-HT2c receptors and leptin may be involved in the effects of corticosterone-induced hyperphagia.


Appetite Regulation/drug effects , Corticosterone/pharmacology , Hypothalamus/drug effects , Leptin/agonists , Nerve Tissue Proteins/metabolism , Neurons/drug effects , Receptor, Serotonin, 5-HT2C/metabolism , Animals , Appetite Depressants/chemistry , Appetite Depressants/pharmacology , Appetite Stimulants/administration & dosage , Appetite Stimulants/agonists , Appetite Stimulants/antagonists & inhibitors , Appetite Stimulants/pharmacology , Behavior, Animal/drug effects , Corticosterone/administration & dosage , Corticosterone/agonists , Corticosterone/antagonists & inhibitors , Dose-Response Relationship, Drug , Energy Intake/drug effects , Hyperphagia/blood , Hyperphagia/chemically induced , Hyperphagia/metabolism , Hyperphagia/pathology , Hypothalamus/metabolism , Hypothalamus/pathology , Leptin/antagonists & inhibitors , Leptin/blood , Leptin/metabolism , Mice, Inbred ICR , Nerve Tissue Proteins/agonists , Nerve Tissue Proteins/antagonists & inhibitors , Nerve Tissue Proteins/genetics , Neurons/metabolism , Neurons/pathology , Organ Specificity , Piperazines/antagonists & inhibitors , Piperazines/pharmacology , Proto-Oncogene Proteins c-fos/agonists , Proto-Oncogene Proteins c-fos/genetics , Proto-Oncogene Proteins c-fos/metabolism , Receptor, Serotonin, 5-HT2C/chemistry , Serotonin 5-HT2 Receptor Agonists/pharmacology , Serotonin 5-HT2 Receptor Antagonists/pharmacology , Spiro Compounds/pharmacology , Sulfonamides/pharmacology , Up-Regulation/drug effects
4.
PLoS One ; 9(4): e93158, 2014.
Article En | MEDLINE | ID: mdl-24690630

Recently, studies have shown that serotonin plays an important role in the control of seizure. However, the specific role of 5-HT receptor subtypes is not yet well described, in particular that of the 5-HT3 receptor. The present study was aimed to investigate the role of 5-HT3 receptor on the pentylenetetrazole (PTZ)-induced seizure in mice. Firstly, seizure latency was significantly prolonged by a 5-HT3 receptor agonist SR 57227 in a dose-dependent manner. Seizure score and mortality were also decreased by SR 57227 in PTZ-treated mice. Furthermore, these anticonvulsant effects of SR 57227 were inhibited by a 5-HT3 receptor antagonist ondansetron. However, ondansetron alone had no effect on seizure latency, seizure score or mortality at different doses. Immunohistochemical studies have also shown that c-Fos expression was significantly increased in hippocampus (dentate gyrus, CA1, CA3 and CA4) of PTZ-treated mice. Furthermore, c-Fos expression was significantly inhibited by ondansetron in mice treated with PTZ and SR 57227. An ELISA study showed that SR 57227 attenuated the PTZ-induced inhibitory effects of GABA levels in hippocampus and cortex, and the attenuated effects of SR 57227 were antagonized by ondansetron in hippocampus but not cortex. Our findings suggest that activation of 5-HT3 receptor by SR 57227, which plays an important role on the control of seizure induced by PTZ, may be related to GABA activity in hippocampus. Therefore, 5-HT3 receptor subtype is a potential target for the treatment of epilepsy.


Anticonvulsants/therapeutic use , Piperidines/therapeutic use , Seizures/chemically induced , Seizures/drug therapy , Animals , Anticonvulsants/pharmacology , Hippocampus/drug effects , Hippocampus/metabolism , Hippocampus/pathology , Male , Mice, Inbred ICR , Ondansetron/pharmacology , Ondansetron/therapeutic use , Pentylenetetrazole , Piperidines/pharmacology , Proto-Oncogene Proteins c-fos/metabolism , Survival Analysis , gamma-Aminobutyric Acid/metabolism
5.
Article En | MEDLINE | ID: mdl-24036107

Recently, studies show that intermittent fasting and caloric restriction may improve symptoms of depression. However, there is little scientific evidence regarding the literature on the antidepressant-like effects of acute fasting. The present study aims to investigate the antidepressant-like effects and its influence on brain levels of the transcription factor cAMP response element-binding protein (CREB) and its phosphorylated form (p-CREB) in different time periods of fasting mice. Furthermore, the additive antidepressant-like effects of fasting with imipramine and the possible involvement of the 5-HT2 receptors were examined. In the present study 9h, but not 3h and 18h of fasting significantly reduced immobility time in the forced swimming test (FST) without alteration in locomotor activity in the open field test. 9h fasting also enhanced the ratio of p-CREB/CREB in the frontal cortex and hippocampus. Co-administration of 9h of fasting and imipramine (30mg/kg, i.p) produced the additive antidepressant-like effects in the FST and increased the ratio of p-CREB/CREB. Meanwhile, the additive effects were partially reversed by treatment with a 5-HT2A/2C receptor agonist, (±)-1-(2, 5-dimethoxy-4-iodophenyl)-2-aminopropane hydrochloride (DOI) (5mg/kg, s.c). Furthermore, the antidepressant-like effects of 9h fasting was also blocked by DOI compared to the non-fasting control group. Serum corticosterone level, but not 5-HT and noradrenaline, was significantly increased in a time-dependent manner following different time periods of fasting. Taken together, these results suggest that acute fasting produces antidepressant-like effects via enhancement of the p-CREB/CREB ratio, and additive antidepressant-like effects of fasting with imipramine may be related to modulating 5-HT2 receptors.


Antidepressive Agents, Tricyclic/pharmacology , Brain/drug effects , Brain/metabolism , Fasting , Imipramine/pharmacology , Receptors, Serotonin, 5-HT2/metabolism , Amphetamines/pharmacology , Animals , CREB-Binding Protein/metabolism , Corticosterone/blood , Gene Expression Regulation/drug effects , Immobility Response, Tonic/drug effects , Male , Mice , Mice, Inbred ICR , Motor Activity/drug effects , Norepinephrine/blood , Serotonin/blood , Serotonin Receptor Agonists/pharmacology , Time Factors
6.
J Pharmacol Sci ; 123(2): 195-8, 2013.
Article En | MEDLINE | ID: mdl-24096829

We investigated the anticonvulsant effect of acute Fuzi total alkaloid (FTA) in seizure induced by the GABAA-receptor antagonist pentylenetetrazole (PTZ). FTA significantly increased the seizure latency and decreased the mortality in PTZ-treated mice. Administration of PTZ increased c-Fos expression in the hippocampus, medial prefrontal cortex, and piriform cortex; and this PTZ-induced effect was inhibited by FTA in a dose-dependent manner. Furthermore, the effects of FTA on PTZ-induced seizure and c-Fos expression were reversed by the GABAA/benzodiazepine receptor-selective antagonist flumazenil. These findings suggest that the anticonvulsant effects of FTA may be related to modulation of GABAA-benzodiazepine receptor complex.


Anticonvulsants/pharmacology , GABA-A Receptor Antagonists , Pentylenetetrazole , Phytotherapy , Plant Extracts/pharmacology , Receptors, GABA-A/metabolism , Seizures/chemically induced , Seizures/drug therapy , Animals , Cerebral Cortex/metabolism , Disease Models, Animal , Diterpenes , Dose-Response Relationship, Drug , Drugs, Chinese Herbal , Flumazenil/pharmacology , Hippocampus/metabolism , Male , Mice , Mice, Inbred ICR , Pentylenetetrazole/antagonists & inhibitors , Proto-Oncogene Proteins c-fos/metabolism , Seizures/metabolism
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