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1.
Shanghai Kou Qiang Yi Xue ; 33(1): 80-84, 2024 Feb.
Article in Chinese | MEDLINE | ID: mdl-38583030

ABSTRACT

PURPOSE: To investigate the effect of endoscopy-aided non-incisional periodontal regeneration technique (NIT) in the treatment of alveolar bone angular resorption. METHODS: Thirteen patients with severe periodontitis(13 diseased teeth) were selected. All patients had alveolar bone angular resorption on adjacent surface. The patients received NIT treatment 6 weeks after periodontal primary therapy. The visualization of subgingival environment was acquired by the periodontal endoscopy. Following the removal of the subgingival plaque, calculus and intra-bony granulation tissue, bone grafting materials were placed into the intra-bony defects with the assistance of a delicate gingival protector. No flap was elevated and no sutures were applied. Probing depth (PD), gingival recession (GR), clinical attachment level (CAL), as well as radiographic parameters were evaluated at baseline and 2 years after treatment. SPSS 22.0 software package was used for data analysis. RESULTS: At 2-years follow-up, an average CAL gain of (3.65±2.10) mm (P<0.001), PD reduction of (4.42±1.66) mm (P<0.001), and minimal increase in GR of (0.38±0.87) mm (P=0.25) were observed. Alveolar bone was significantly improved at 2-years follow-up on radiographs (P<0.001). CONCLUSIONS: For angular resorption site of alveolar bone, NIT treatment can obtain good periodontal regeneration results without flap inversion.


Subject(s)
Alveolar Bone Loss , Gingival Recession , Periodontitis , Humans , Follow-Up Studies , Periodontal Pocket/surgery , Periodontitis/diagnostic imaging , Periodontitis/surgery , Alveolar Bone Loss/diagnostic imaging , Alveolar Bone Loss/surgery , Alveolar Process/surgery , Gingival Recession/surgery , Endoscopy , Guided Tissue Regeneration, Periodontal/methods , Periodontal Attachment Loss/surgery , Treatment Outcome , Bone Regeneration
2.
Aging Clin Exp Res ; 35(11): 2323-2331, 2023 Nov.
Article in English | MEDLINE | ID: mdl-37776484

ABSTRACT

BACKGROUND: The prophylactic effect of exogenous melatonin and melatonin receptor agonists (MMRAs) on postoperative delirium (POD) in elderly patients remains controversial. OBJECTIVE: This study aimed to assess the prophylactic effect of MMRAs on POD by conducting a systemic review and meta-analysis of randomized controlled trials (RCTs). METHODS: We systematically searched four electronic databases including PubMed, Web of Science, Cochrane Library, and Embase for the eligible studies up to February 28, 2023. The Cochrane risk of bias tool was used for assessing the risk of bias in the included RCTs. The occurrence of POD was the primary outcome. The quality of evidence was evaluated by Grading of Recommendations Assessment, Development, and Evaluation. RESULTS: A total of 11 RCTs comprising patients (MMRA group: 777 patients and placebo group: 781 patients) were included. The results of the meta-analysis showed that the MMRA group had a lower occurrence of POD than the placebo group (risk ratio = 0.70, 95% confidence interval: 0.51-0.97, P < 0.05, I2 = 59%). The subgroup analysis showed that melatonin significantly reduced the occurrence of POD (moderate-quality evidence), whereas ramelteon and tryptophan had no significant impact (moderate-quality evidence). CONCLUSION: Existing evidence suggested that perioperative use of melatonin can prevent POD in elderly patients.


Subject(s)
Emergence Delirium , Melatonin , Humans , Aged , Emergence Delirium/prevention & control , Melatonin/therapeutic use , Receptors, Melatonin , Randomized Controlled Trials as Topic , Hypnotics and Sedatives
3.
World J Clin Cases ; 10(14): 4550-4562, 2022 May 16.
Article in English | MEDLINE | ID: mdl-35663057

ABSTRACT

BACKGROUND: Treating periodontally hopeless teeth with advanced bone resorption and severe tooth mobility is a great challenge for both orthodontists and periodontists. Biofilm-induced periodontal inflammation and occlusal trauma-related inflammation may synergistically aggravate tooth mobility. This case report illustrates that even periodontally hopeless teeth can be saved and have long-term stability with comprehensive periodontal treatment to control periodontal inflammation and promote periodontal bone regeneration and intricate orthodontic mechanical control to correct cross bite and occlusal trauma. CASE SUMMARY: A 27-year-old female patient whose chief complaint was severe tooth mobility and discomfort of the maxillary incisor was diagnosed with severe aggressive periodontitis by clinical and radiographic examinations. To reduce tooth mobility and establish stable occlusion, we combined orthodontic treatment with periodontal therapy to preserve the tooth. Orthodontic treatment was performed after basic periodontal therapy and periodontal surgery. The loosened upper right central incisor was successfully retained, and the periodontal tissue remained stable during follow-up. CONCLUSION: Teeth with severe mobility and bone loss can be saved through interdisciplinary treatment when periodontal inflammation is strictly controlled.

4.
Pharmacology ; 102(5-6): 300-306, 2018.
Article in English | MEDLINE | ID: mdl-30253391

ABSTRACT

Remifentanil-induced hyperalgesia (RIH) is known to be associated with oxidative stress and inflammation. Betulinic acid (BA) was reported to reduce visceral pain owing to its anti-oxidative and anti-inflammatory potential. Here, we -explored whether BA can attenuate RIH through inhibiting oxidative stress and inflammation in spinal dorsal horn. Sprague-Dawley rats were randomly divided into 4 groups: Control, Incision, RIH, and RIH pre-treated with BA. After pretreated with BA (25 mg/kg, i.g.) for 7 days, rats were subcutaneously infused with remifentanil (40 µg/kg) for 30 min during right plantar incision surgery to induce RIH. The paw withdrawal mechanical threshold (PWMT), paw withdrawal thermal latency (PWTL), spinal oxidative stress and inflammatory mediators were determined. Intraoperative remifentanil infusion induced postoperative hyperalgesia, as evidenced by the significant decrease in PWMT and PWTL (p < 0.01), and the significant increase in oxidative stress and inflammation evidenced by up-regulations of malondialdehyde, 3-nitrotyrosine, interleukin-1ß and tumour necrosis factor-α (p < 0.01) in spinal dorsal horn and matrix metalloproteinase-9 (MMP-9) activity (p < 0.01) in dorsal root ganglion, as well as a decrease in manganese superoxide -dismutase activity (p < 0.01) compared with control and -incision groups. All these results mentioned above were markedly reversed by pre-treatment with BA (p < 0.01) compared with RIH group. These findings demonstrated that BA can effectively attenuate RIH, which associates with potentially inhibiting oxidative stress and subsequently down-regulating MMP-9-related pro-inflammatory cyokines in spinal dorsal horn.


Subject(s)
Hyperalgesia/chemically induced , Hyperalgesia/drug therapy , Inflammation/drug therapy , Oxidative Stress/drug effects , Remifentanil/antagonists & inhibitors , Spinal Cord Dorsal Horn/drug effects , Triterpenes/pharmacology , Animals , Anti-Inflammatory Agents, Non-Steroidal/pharmacology , Drug Interactions , Ganglia, Spinal/drug effects , Ganglia, Spinal/metabolism , Ganglia, Spinal/pathology , Hyperalgesia/metabolism , Inflammation/metabolism , Inflammation/pathology , Interleukin-1beta/metabolism , Male , Pain, Postoperative/drug therapy , Pentacyclic Triterpenes , Random Allocation , Rats , Rats, Sprague-Dawley , Remifentanil/toxicity , Spinal Cord Dorsal Horn/metabolism , Spinal Cord Dorsal Horn/pathology , Superoxide Dismutase/metabolism , Tumor Necrosis Factor-alpha/metabolism , Tyrosine/analogs & derivatives , Tyrosine/metabolism , Betulinic Acid
5.
PLoS One ; 7(8): e40930, 2012.
Article in English | MEDLINE | ID: mdl-22879882

ABSTRACT

There is accumulating evidence to implicate the importance of EphBs receptors and ephrinBs ligands were involved in modulation of spinal nociceptive information. However, the downstream mechanisms that control this process are not well understood. In the present study, we investigated whether phosphatidylinositol 3-kinase (PI3K), as the downstream effectors, participates in modulation of spinal nociceptive information related to ephrinBs/EphBs. Intrathecal injection of ephrinB1-Fc produced a dose- and time-dependent thermal and mechanical hyperalgesia, accompanied by the increase of spinal PI3K-p110γ, phosphorylation of AKT (p-AKT) and c-Fos expression. Pre-treatment with PI3K inhibitor wortmannin or LY294002 prevented activation of spinal AKT induced by ephrinB1-Fc. Inhibition of spinal PI3K signaling dose-dependently prevented and reversed pain behaviors and spinal c-Fos protein expression induced by intrathecal injection of ephrinB1-Fc. Inhibition of EphBs receptors by intrathecal injection of EphB1-Fc reduced formalin-induced inflammation and chronic constrictive injury-induced neuropathic pain behaviors accompanied by decreased expression of spinal PI3K,p-AKT and c-Fos protein. Furthermore, pre-treatment with PI3K inhibitor wortmannin or LY294002 prevented ephrinB1-Fc-induced ERK activation in spinal. These data demonstrated that PI3K and PI3K crosstalk to ERK signaling contributed to modulation of spinal nociceptive information related to ephrinBs/EphBs.


Subject(s)
Ephrin-B1/pharmacology , Nociception , Phosphatidylinositol 3-Kinase/metabolism , Receptors, Eph Family/metabolism , Spinal Cord/enzymology , Spinal Cord/pathology , Animals , Disease Models, Animal , Enzyme Activation/drug effects , Ephrin-B1/administration & dosage , Ephrin-B1/therapeutic use , Extracellular Signal-Regulated MAP Kinases/metabolism , Humans , Hyperalgesia/complications , Hyperalgesia/drug therapy , Hyperalgesia/enzymology , Hyperalgesia/pathology , Inflammation/complications , Inflammation/drug therapy , Inflammation/enzymology , Inflammation/pathology , Injections, Spinal , Male , Mice , Neuralgia/complications , Neuralgia/drug therapy , Neuralgia/enzymology , Neuralgia/pathology , Nociception/drug effects , Phosphoinositide-3 Kinase Inhibitors , Phosphorylation/drug effects , Proto-Oncogene Proteins c-akt/metabolism , Proto-Oncogene Proteins c-fos/metabolism , Spinal Cord/drug effects , Time Factors
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