Isolation and characterization of a hepatoprotective polysaccharide from Lonicera caerulea L. var. edulis Turcz. ex Herd. fruit against APAP-induced acute liver injury mice.

The structure and bioactivities of a novel polysaccharide from Lonicera caerulea L. var. edulis Turcz. ex Herd. fruit (THP-3) were investigated. The crude polysaccharides of Turcz. ex Herd. (THP) were extracted by hot water extraction. After purification, the chemical structure of polysaccharides was identified. Then, a mouse model of acute drug-induced liver injury was constructed using 4-acetamidophenol (APAP) and pretreated with THP. The number-average molecular weight of THP-3 was 48.89 kDa and the mass average molar mass was 97.87 kDa. THP-3 was mainly composed of arabinose (42.54 %), glucose (27.62 %), galacturonic acid and galactose (29.84 %). The main linkage types of THP-3 were 1-linked Araf, 1,4-linked Glcp, and 1,3,6-linked Galp. In addition, after THP treatment, serum Alanine aminotransferase (ALT), Aspartate aminotransferase (AST) and γ-glutamyl transpeptidase (γGT) in AILI mice were successfully down-regulated. The results showed that THP could prevent the characteristic morphological changes of hepatic lobular injury and lipid depletion caused by APAP, reduced the level of oxidative damage in mice, increased the expression of APAP-induced hypolipidemia and related inflammatory indicators, and improved the detoxification function of liver. In general, the newly extracted THP polysaccharide has a good liver protection effect and is an ideal natural medicine for the treatment of liver diseases.

Nobiletin Alleviated Epithelial-Mesenchymal Transition of Hepatocytes in Liver Fibrosis Based on Autophagy-Hippo/YAP Pathway.

SCOPE: The current researches indicated that the epithelial-mesenchymal transition (EMT) of hepatocytes plays a crucial role in the development of liver fibrosis. To date, there is a paucity of literature regarding the impact of nobiletin (NOB) on liver fibrosis. This study investigates the inhibitory effect of NOB on EMT in hepatocytes during the progression of liver fibrosis and its underlying mechanism. METHODS AND RESULTS: The findings demonstrated that NOB significantly suppresses liver fibrosis in carbon tetrachloride (CCl4 )-induced mice by reducing inflammation and fiber deposition in the liver. Moreover, NOB mitigates EMT in hepatocytes, concurrently alleviating inflammatory status and reducing the production of reactive oxygen species (ROS) generation. The comprehensive investigation reveals that the hepatoprotective effect of NOB in liver fibrosis is attributed to autophagy activation, as evidenced by a significant increase in LC3 II expression and p62 degradation upon NOB treatment. Additionally, NOB activates the Hippo/YAP pathway by downregulating YAP and its downstream targets in liver fibrosis, which is regulated by autophagy based on experiments with chloroquine (CQ), 3-methyladenine (3-MA), and siYAP intervention. CONCLUSION: Therefore, this study provides evidences that NOB can protect hepatocytes from undergoing EMT during liver fibrosis by inducing autophagy and subsequently modulating the Hippo/YAP pathway.

A lipidomic study: Nobiletin ameliorates hepatic steatosis through regulation of lipid alternation.

Hepatic lipidome has been given emphasis for years since hepatic steatosis is the most remarkable character of nonalcoholic fatty liver diseases, an increasingly serious health issue worldwide. Nobiletin (NOB), one of the citrus flavonoids, exerted outstanding effect on lipid metabolism disorder. However, the underlying mechanism of NOB exerting effect on hepatic lipid alternation remains unclear. In this study, the animal model was built by feeding APOE-/- mice with high fat diet (HFD). The results of Oil Red O-stained liver section and the biochemical assay of lipid parameters confirmed the protective effect of NOB on hepatic steatosis and global lipid metabolism disorder in APOE-/- mice. The hepatic lipidomic study revealed a total of 958 lipids significantly altered by HFD and a total of 86, 116, 212 lipid metabolites changed by L-NOB (50 mg/kg/d NOB), M-NOB (100 mg/kg/d NOB) and H-NOB (200 mg/kg/d NOB) respectively. In the further screening analysis, an amount of 60 lipids were identified as the potential lipid markers of NOB treatment, most of which belonged to glycerophospholipids lipid categories and exhibited obvious correlation with each other and the lipid parameters related to hepatic steatosis. Taken together, our data demonstrated that glycerophospholipids metabolism played an indispensable role in the progression of hepatic steatosis and the protective effect of NOB. Besides, the modulation towards genes involved in lipid synthesis was observed after NOB administration in this study. These finding illustrated the antihepatic steatosis effect of NOB based on altering hepatic lipidome, particularly the glycerophospholipids metabolism, and provided a new insight in the pathogenesis of hepatic steatosis.

Nobiletin mitigates NAFLD via lipophagy and inflammation.

Nonalcoholic fatty liver disease (NAFLD), an increasingly serious health issue around the world, is characterized as a lipid metabolic disorder without any satisfactory treatment. Nobiletin (NOB), a citrus flavonoid, is considered a promising candidate for NAFLD prevention although there is limited research towards its exact mechanism. In this study, the preventative effect of NOB on NAFLD was investigated using high fat diet-fed ApoE-/- mice and free fatty acid-treated HepG2 cells. The results of hematoxylin and eosin staining of liver sections revealed that L-NOB (50 mg kg-1 d-1 NOB), M-NOB (100 mg kg-1 d-1 NOB) and H-NOB (200 mg kg-1 d-1 NOB) could significantly ameliorate NAFLD. Further exploration illustrated that NOB alleviated hepatic steatosis mainly via TFEB-mediated lysosomal biogenesis and lipophagy. Besides, NOB could mitigate NLRP3 inflammasome assembly and modulate M1/M2 macrophage polarization in vivo and in vitro. The mechanisms above allowed NOB to attenuate NAFLD, but their close association needed further investigation. Our research not only illustrated NOB as a potential candidate for NAFLD prevention, but also provided new insight into the pathogenic mechanisms of NAFLD development.

Lightweight Porous Polyurethane Foam Integrated with Graphene Oxide for Flexible and High-Concentration Hydrogen Sensing.

Reliable detection of high-concentration hydrogen (H2) leakage in sharp-vibration environments is highly desired such as in the application of space rockets. As hydrogen has to be detected simultaneously in a wide concentration range and at high concentrations (e.g., 100 v/v%) with outstanding linearity in response/concentration, lightweight features, and excellent tolerance against saturation and vibration, it remains challenging. Here, a flexible and high-concentration H2 sensing has been developed through "dipping-drying" a three-dimensional (3D) porous polyurethane (PU) foam integrated with graphene oxide (GO-PU). Multilayered honeycomb-structured graphene oxide appears to be tightly adhered to faveolate PU. Benefiting from the numerous adsorption sites of the "dual honeycomb" structure and abundant surface functional groups of GO, the GO-PU foam exhibits distinguished response and linearity toward 2-100 v/v% H2 and shows excellent lightweight, tailorability, and flexibility. Remarkably, the foam possesses outstanding sensing stability against 0-180° bending and low 0-20% straining, along with outstanding H2 sensing performance even after being pressed by a weight of 200 g, immersed in water, and frozen in a refrigerator at -10.8 °C. Practically, the GO-PU foam has potential for high-concentration H2 leakage detection, and our synthetic strategy may provide a way to avoid adsorbing saturation in other flexible gas sensing.

Three-Dimensional Porous Carbon/Nitrogen Framework-Decorated Palladium Nanoparticles for Stable and Wide-Concentration-Range Hydrogen Sensing.

Hydrogen (H2) as a high-energy-density carrier is of great potential in the upcoming hydrogen economy. Nevertheless, H2/air mixtures are explosive at H2 concentrations above 4 v/v % and reliable and wide-concentration-range H2 sensors are thus highly desired. Here, hydrogen sensing has been developed using palladium nanoparticles of ∼11.2 nm in diameter chemically decorated on the carbon/nitrogen three-dimensional porous framework of 308 m2 g-1 in specific surface area (Pd NPs@CN 3D framework). Theoretically, the Pd NPs and CN 3D framework are used to construct the Mott-Schottky heterojunctions, in which the CN 3D framework possesses a higher work function, promoting electron transfer to Pd NPs and therefore highly active dissociation of H2. Beneficially, the Pd NPs@CN 3D framework exhibits a wide concentration range of 200 ppm (S ≈ 0.2% and Tres ≈ 15 s) to 40 v/v % (S ≈ 73.8% and Tres ≈ 9 s) H2 sensing at room temperature. Remarkably, the H2 sensor prototype built with the Pd NPs@CN 3D framework shows excellent long-term stability that maintains reliable H2 sensing after 142 days. Such stable hydrogen sensing provides an experimental basis for the wide-concentration-range detection of H2 leakage in the future hydrogen economy.

Nanocomposite-Decorated Filter Paper as a Twistable and Water-Tolerant Sensor for Selective Detection of 5 ppb-60 v/v% Ammonia.

Ammonia (NH3) sensors proposed for the simultaneous exhalation diagnosis, environmental pollution monitoring, and industrial leakage alarm require high flexibility, selectivity, stability, humidity tolerance, and wide-concentration-range detection; however, technical challenges still remain. Herein, twistable and water-tolerant paper-based sensors integrated over surgical masks have been developed for NH3 detection at room temperature, via decorating specially designed ternary nanocomposites (ternary-NCs) on the commercial filter paper. The NCs consist of a multiwalled carbon nanotube framework with a polypyrrole nanolayer and are further loaded with Pt nanodots. Benefiting from the synergy effect of ternary components, the ternary-NCs exhibit an ultrasensitive response to 5 ppb-60 v/v% NH3 and present high selectivity confirmed by the theory calculations. Remarkably, the filter-paper-based sensors possess outstanding stability against twisting 0-1080°, along with excellent cuttability and foldability. Critically, such paper-based sensors can be integrated over surgical masks for simulated exhaled diagnosis and display superior water tolerance even being immersed in water for 24 h. Practically, the detecting accuracy of the filter-paper-based sensor toward the simulated exhaled NH3, environmental NH3 pollution, and industrial NH3 leakage is validated using ion chromatography.

Radial ZnO nanorods decorating Co3O4 nanoparticles for highly selective and sensitive detection of the 3-hydroxy-2-butanone biomarker.

Indirect monitoring of Listeria monocytogenes (LM) via a gas sensor that can detect the bacterial metabolite 3-hydroxy-2-butanone (3H-2B) is a newly emerged strategy. However, such sensors are required simultaneously endow with outstanding selectivity, high sensitivity, and ppb-level detection limit, which remains technologically challenging. Herein, we have developed highly selective and sensitive 3H-2B sensors that consist of zinc oxide nanorods decorated with cobaltosic oxide nanoparticles (ZnO NRs/Co3O4 NPs), which have been synthesized by combined optimized hydrothermal and annealing process. Specifically, the ZnO NRs/Co3O4 NPs exhibit ultrahigh sensitivity to 5 ppm 3H-2B (Ra/Rg = 550 at 260 °C). The sensor prototypes enable detection as low as 10 ppb 3H-2B, show excellent long-term stability, and present remarkable selectivity through interfering selectivity survey and principal component analysis (PCA). Such outstanding sensing performance is attributed to the modulated electron depletion layer by n-p heterojunctions and abundant gas diffusion pathways via the radial architecture, which was verified via electrochemical impedance spectroscopy test, Mott-Schottky measurement, and ultraviolet-visible absorption analysis. Our highly selective and sensitive ZnO NRs/Co3O4 NPs have the potential in the real-time detection of 3H-2B biomarker.

The "screening behavior" of lithium: Boosting H2S selectivity of WO3 nanofibers.

An ideal way to boost the selectivity of sensing materials is that improving the sensitivity of the target gas while suppressing that of other interfering ones. Here, the "screening behavior" of the Li doped WO3 nanofibers (Li/WO3 NFs) have been discovered in suppressing the response from interfering gases, while elevating the H2S sensing response. Beneficially, the H2S response of Li/WO3 NFs sensor prototype is three times (Ra / Rg = 64@10 ppm) as high as that of the pristine WO3 ones (Ra / Rg = 21@10 ppm) at ~75% relative humidity and 260 °C. Moreover, Li/WO3 NFs sensor prototype presents the detection limit as low as 100 ppb. Particularly, the Li/WO3 NFs sensors detect simulated halitosis breath, of which the accuracy is comparable with gas chromatography. Theoretically, the decrease of the responses of Li/WO3 NFs to interfering gases is ascribed to the enhancement of the adsorption of water molecules by Li dopant. While the improved response to H2S is attributed to stronger adsorption of H2S and WO3 and to the increased defect oxygen. The "screening behavior" of Li doped into WO3 NFs provides a new strategy that might improve the selectivity of other gas sensing.

Highly sensitive and fast-response hydrogen sensing of WO3 nanoparticles via palladium reined spillover effect.

Hydrogen sensing simultaneously endowed with fast response, high sensitivity and selectivity is highly desired in detecting hydrogen leakages such as in hydrogen-driven vehicles and space rockets. Here, hydrogen sensing reined via a hydrogen spillover effect has been developed using palladium nanoparticles photochemically decorated on WO3 nanoparticles (Pd-NPs@WO3-NPs). Theoretically, the Pd-NP catalysts and WO3-NP support are used to construct the hydrogen spillover system, in which Pd NPs possess high catalytic activity, promoting the electron transfer and therefore the reaction kinetics. Beneficially, the Pd-NPs@WO3-NP sensor prototypes toward 500 ppm hydrogen simultaneously exhibit fast response time (∼1.2 s), high response (Ra/Rg = 22 867) and selectivity at a working temperature of 50 °C. Such advanced hydrogen sensing provides an experimental basis for the smart detection of hydrogen leakage in the future hydrogen economy.

Highly Sensitive and Selective NiO/WO3 Composite Nanoparticles in Detecting H2S Biomarker of Halitosis.

Indirectly monitoring halitosis via the detection of hydrogen sulfide (H2S) biomarkers using gas sensors is a newly emerging technique. However, such H2S sensors are required with critically high selectivity and sensitivity, as well as a ppb-level detection limit, which remains technologically challenging. To address such issues, here, we have developed highly sensitive and selective H2S sensors with NiO/WO3 nanoparticles (NPs), which have been synthesized by firstly hydrolyzing WO3 NPs and subsequently decorating with NiO NPs in a hydrothermal process. Theoretically, the NiO/WO3 NPs assist in forming a thicker electron depletion layer, adsorbing more oxygen species O2- to oxidize H2S and finally release more electrons. Beneficially, 2.1 wt % NiO/WO3 NPs show high sensitivity to H2S (Ra/Rg = 15031 ± 1370 @ 10 ppm, 100 °C), which is 42.6-fold higher than that of the pristine WO3 NPs (Ra/Rg = 353 ± 5.6 @ 10 ppm, 100 °C). Further, the H2S sensor shows ppb-level detection limit (Ra/Rg = 4.95 ± 2.9 @ 0.05 ppm, 100 °C) and high selectivity. Practically, NiO/WO3 NP sensor prototype has been employed to detect the simulated exhaled halitosis compared with that of gas chromatography, revealing a close concentration of H2S. Our investigation offers an experimental base in future intelligent medical applications.

Gas Sensor Detecting 3-Hydroxy-2-butanone Biomarkers: Boosted Response via Decorating Pd Nanoparticles onto the {010} Facets of BiVO4 Decahedrons.

The newly emerged gas sensing detection of 3-hydroxy-2-butanone (3H-2B) biomarker is deemed as an effective avenue to indirectly monitor Listeria monocytogenes (LM). However, 3H-2B sensing materials requiring critically high sensitivity and selectivity, and ppb-level detection limit, remain challenging. Here, we report the advanced gas sensors built with bismuth vanadate microdecahedron (BiVO4 MDCD) {010} facets selectively decorated with Pd nanoparticles (Pd NPs, Pd-{010}BiVO4 MDCDs) for boosted detection of the 3H-2B biomarker. Meanwhile, BiVO4 MDCDs with overall facets are randomly deposited with Pd NPs (Pd-BiVO4 MDCDs). Comparatively, Pd-{010}BiVO4 MDCD sensors show 1 order of magnitude higher response toward the 3H-2B biomarker at 200 °C. Further, Pd-{010}BiVO4 MDCD sensors enable to detect as low as 0.2 ppm 3H-2B and show best selectivity and stability, and fastest response and recovery. Density functional theory calculations reveal a lower adsorption energy of 3H-2B onto Pd-{010}BiVO4 MDCDs than those of pristine and Pd-BiVO4 MDCDs. The extraordinary Pd-{010}BiVO4 sensing performance is ascribed to the Pd NP-assisted synergetic effect of the preferential adsorption of 3H-2B target molecules, accumulated sensing agent of ionic oxygen species, and concentrated catalysts on the {010} facets. This strategy offers rapid and noninvasive detection of LMs and is thus of great potential in the upcoming Internet of Things.

Palladium/cobalt nanowires with improved hydrogen sensing stability at ultra-low temperatures.

The metallic dopants in palladium (Pd) sensing materials enable modification of the d-band center of Pd, which is expected to tune the α-ß phase transitions of the PdHx intermediate, thus improve the sensing stability to hydrogen. Here, the boosted hydrogen-sensing stability at ultra-low temperatures has been achieved with palladium/cobalt nanowires (PdCo NWs) as the sensing material. The various Co contents in PdCo NWs were modulated via AAO-template-confined electrodeposition. The temperature-dependent sensing evaluations were performed in 0.1-3 v/v% hydrogen. Such sensors integrated with PdCo NWs are able to stably detect hydrogen as low as 0.1 v/v%, even when the temperature is lowered to 273 K. In addition, the critical temperatures of "reverse sensing behavior" of the PdCo NWs (Pd82Co18: Tc = 194 K; Pd63Co37: Tc = 180 K; Pd33Co67: Tc = 184 K) are observed much lower than that of pristine Pd NWs (Tc = 287 K). Specifically, the Pd63Co37 NWs (∼37 at% Co content) sensor shows outstanding stability of sensing hydrogen against α-ß phase transitions within the wide temperature range of 180-388 K, which is attributed to both the electronic interactions between Pd and Co and the lattice compression strain caused by Co dopants. Moreover, the "reverse sensing behavior" of the PdCo NWs is explicitly interpreted using the α-ß phase transition model.

Interconnected Pd Nanoparticles Supported on Zeolite-AFI for Hydrogen Detection under Ultralow Temperature.

The stability for a hydrogen sensor is of crucial importance under a low-temperature range (e.g., 200-400 K), especially in critical environments (e.g., aerospace). However, the "reverse sensing behavior" of Pd-based sensing materials at low temperatures limits their wide application. Herein, a three-dimensional (3D) hydrogen-sensing material of interconnected Pd nanoparticles supported on zeolite-AFI (zeolite-AFI@Pd NPs) is designed for the hydrogen sensor at low temperature. The interconnected Pd NPs of ∼15 nm in diameter are achieved onto the zeolite-AFI framework by reduction-controlled self-assembly growth, followed by partially etching-off zeolite. The 3D structure provides a larger surface ratio for improving hydrogen adsorption onto Pd, and more space for PdHx intermediate expansion, which effectively facilitates response to hydrogen and suppresses the α-ß phase transition. Remarkably, there is no "reverse sensing behavior" observed in zeolite-AFI@Pd NPs, though temperature is as low as to 200 K compared with that of pristine Pd nanowires at 287 K. Furthermore, the zeolite-AFI@Pd NPs sensors yield excellent sensing response and high stability to hydrogen at temperature from 200 to 400 K. Such Zeolite-AFI@Pd NPs sensors are expected to detect hydrogen leakage, especially in critical environments of low temperature.

Autophagy plays a protective role in motor neuron degeneration following spinal cord ischemia/reperfusion-induced spastic paralysis.

Spinal cord ischemia and reperfusion (SCIR) injury can lead to neurologic dysfunction and paraplegia, which are serious complications after shock or thoracoabdominal aortic surgery. Autophagy is a fundamental cellular process in eukaryotes, and homeostasis of autophagic activities in the cytoplasm is critical for the maintenance of neuronal function. To date, no studies have addressed the involvement of autophagy in the regulation of motor neurons in the ventral horn of the spinal cord area following SCIR-induced spastic paralysis or the underlying mechanisms of this process. In this study, we investigated spastic paralysis in rats following SCIR injury. The number of autophagosomes increased 3 h following the injury, and subsequently decreased slowly to near-normal levels in the sham group as indicated by the autophagy markers microtubule-associated protein 1 light chain 3 (LC3), beclin-1, and p62. Furthermore, after treatment with the autophagy inhibitor 3-Methyladenine (3-MA) and autophagy activator rapamycin following SCIR, autophagy in the SCIR-3-MA group decreased significantly, while that in the SCIR-Rap group increased, compared with SCIR-DMSO controls group. Moreover, the assessment of motor neurons function, using Reuter's score and motor evoked potentials (MEP) and somatosensory evoked potentials (SEP), indicated that promoting autophagy reduced scores compared with SCIR controls, while inhibiting autophagy increased the scores, and hence motor neurons function. Autophagy in the SCIR model protected motor neurons function and morphology. These results would provide more evidences for better understanding function of autophagy in motor neurons degeneration and mechanisms underlying spastic paralysis. Autophagy would be a novel target for prevention and therapy in SCIR damage.

Motor neuron degeneration following glycine-mediated excitotoxicity induces spastic paralysis after spinal cord ischemia/reperfusion injury in rabbit.

Spinal cord ischemia and reperfusion (SCIR) injury is the major cause of a wide range of complications, including neural degeneration and devastating paraplegia. Decrease of inhibitory neurotransmitters and increase of excitory neurotransmitters are the major cause for the excitotoxicity of neurons. However, no study has reported the temporal loss of motor neuron in the ventral horn of spinal cord area following SCIR-induced spastic paralysis, not even the mechanism under it. In the present study, we found that the rabbits were mainly spastic paralyzed after spinal cord ischemia-reperfusion injury. And the ischemia 60 min group is the optimal treating condition, because of the higher rate of spastic paralysis and lower mortality. Motor neurons in the ventral horn of spinal cord were significant degeneration at 3 h following spastic paralysis and only 12.5% motor neurons were observed at 72 h post-operation, compared with control group. ELISA results indicated that Glycine and GABA were both downregulated following spastic paralysis. But Glycine immediately decreased at 10 min post-operation and lasted for the whole process (at least 72 h). Meanwhile GABA only significantly decreased at 72 h. Furthermore, Glutamic expression was significant upregulation at 3 hours post-operation, and the upregulation back to the base level at 72 h post-operation. Glutamic receptor-(NR1) and Glycine α1 receptor upregulated accordingly, whereas GABBR2 didn't upregulate significantly until at 72 h post-operation. Abundant extracellular Ca2+ influxed into cytoplasm in neurons following spastic paralysis. The type of paraplegia is mainly spastic paraplegia after SCIR (ischemia 60 min treatment). Following spastic paraplegia, motor neuron in the ventral horn of spinal cord area was significant degeneration at early stage and last for the whole process. It may contribute to the decrease of Glycine at early stage and followed exitotoxicity, which caused intracellular calcium overload to make neurons dead. It would lay the foundation for better understanding the motor neuron degeneration and mechanism following spastic paralysis. And it would supply a novel and effective target for spastic paralysis prevention and therapy.

Spatiotemporal expression of Ski after rat spinal cord injury.

Ski is an evolutionarily conserved protein and widely participates in the regulation of various pathological and physiological processes such as wound healing, liver regeneration, development of the embryonic nervous system, muscle differentiation, and progression of many kinds of tumors. However, the distribution and function of Ski in central nervous system lesion and disease remain unclear. In this study, we investigated the spatiotemporal expression of Ski in a spinal cord injury (SCI) model in adult rats. Western Blot analysis indicated that Ski was expressed in both normal and injured spinal cord, and showed a significant upregulation after SCI compared with the sham group. Double-labeled immunofluorescence staining showed that Ski was significantly expressed in astrocytes, but not in the neurons. Western Blot analyses of glial fibrillary acidic protein (GFAP) and BBB scores were carried out and correlation analysis showed a positive correlation between them. In addition, the relative expression level of Ski was also positively correlated with the relative expression level of GFAP. Moreover, the conspicuous co-expression band of Ski and GFAP at the lesion border was found in the results of immunofluorescence staining combined with the pattern of glial scar formation reflected by H&E staining; in addition, it was found that Ski was also highly associated with glial scar. On the basis of our data, we speculated that Ski might play an important role in the process of reactive astrogliosis after SCI and our study might provide a basis for further study on the detailed role of Ski in astrocytes.

[Genetic polymorphism of 17 Y-STR loci in four minority populations in Guangxi of China].

To investigate the genetic polymorphism of Y-chromosomal short tandem repeats (STR) loci in Jing, Yi, Yao, and Zhuang minority populations from Guangxi Province, China. 17 Y-STR loci were co-amplified using AmpFlSTR(R) Yfiler PCR Amplification Kit System, and the PCR products were analyzed by genetic analyzer. Cluster and phylogenic tree analyses were conducted to show the genetic distance among the populations. There were 61 different haplotypes in 100 unrelated Yao males, 67 in 105 unrelated Yi males, 79 in 103 unrelated Jing males, and 91 in 107 unrelated Zhuang males. The haplotype diversities of Jing, Yi, Yao and Zhuang were determined as 0.9784, 0.9866, 0.9911, and 0.9956, respectively. Among these 4 minority populations, the genetic distance between Jing and Zhuang was the smallest (0.0391), while the genetic distance between Yi and Yao was the largest (0.3376). The 17 Y-STR loci in the 4 minority populations from Guangxi Province revealed a highly polymorphic genetic distribution, which show a high potential for population genetics and forensic practice.