Juliana Trindade Clemente‐Napimoga

ORCID: 0000-0003-1068-3039
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About
Contact & Profiles
Research Areas
  • Pain Mechanisms and Treatments
  • Inflammatory mediators and NSAID effects
  • Neuropeptides and Animal Physiology
  • Oral microbiology and periodontitis research
  • Peroxisome Proliferator-Activated Receptors
  • Temporomandibular Joint Disorders
  • Botulinum Toxin and Related Neurological Disorders
  • Eicosanoids and Hypertension Pharmacology
  • Adenosine and Purinergic Signaling
  • Bone Metabolism and Diseases
  • Dental Implant Techniques and Outcomes
  • Orthodontics and Dentofacial Orthopedics
  • Salivary Gland Disorders and Functions
  • NF-κB Signaling Pathways
  • Cell Adhesion Molecules Research
  • Pharmacological Effects of Natural Compounds
  • Advancements in Transdermal Drug Delivery
  • Bone health and treatments
  • Macrophage Migration Inhibitory Factor
  • Endodontics and Root Canal Treatments
  • Olfactory and Sensory Function Studies
  • Dental materials and restorations
  • Neuroinflammation and Neurodegeneration Mechanisms
  • Laser Applications in Dentistry and Medicine
  • Osteoarthritis Treatment and Mechanisms

Faculdade São Leopoldo Mandic
2017-2024

Interface (United States)
2023

Universidade Estadual de Campinas (UNICAMP)
2011-2020

Pontifícia Universidade Católica de Campinas
2020

Texas Tech University
2019

Institute of Neuroimmunology of the Slovak Academy of Sciences
2019

Interface (United Kingdom)
2019

Universidade de Uberaba
2006-2012

American Association of Endodontists
2010

MRC Laboratory of Molecular Biology
2009

Bones are widely innervated, suggesting an important role for the sympathetic regulation of bone metabolism, although there controversial studies. We investigated effects propranolol in a model experimental periodontal disease.Rats were assigned as follows: animals without ligature; ligated receiving vehicle and 0.1, 5 or 20 mg·kg(-1) propranolol. After 30 days, haemodynamic parameters measured by cardiac catheterization. Gingival tissues removed assessed IL-1β, TNF-α cross-linked...

10.1111/j.1476-5381.2011.01686.x article EN British Journal of Pharmacology 2011-09-28

Abstract Inflammatory conditions of the temporomandibular joint (TMJ) and peripheral tissues affect many people around world are commonly treated with non-steroidal anti-inflammatory drugs (NSAIDs). However, in order to get desirable results, treatments NSAIDs may take weeks, causing undesirable side effects requiring repeated administration. In this sense, work describes development an optimized nanostructured lipid carrier (NLC) formulation for intra-articular administration naproxen...

10.1038/s41598-019-47486-w article EN cc-by Scientific Reports 2019-08-01

Natural or synthetic ligands for peroxisome proliferator-activated receptor gamma (PPAR-γ) represent an interesting tool pharmacological interventions to treat inflammatory conditions. In particular, PPAR-γ activation prevents pain and inflammation in the temporomandibular joint (TMJ) by decreasing cytokine release stimulating synthesis of endogenous opioids. The goal this study was clarify whether induces macrophage polarization, inhibiting leukocyte recruitment. addition, we investigated...

10.1016/j.intimp.2020.106565 article EN publisher-specific-oa International Immunopharmacology 2020-05-06

Periodontitis is a disease that leads to bone destruction and represents the main cause of tooth loss in adults. The development aggressive periodontitis has been associated with increased inflammatory response induced by presence subgingival biofilm containing Aggregatibacter actinomycetemcomitans. flavonoid quercetin (1) widespread vegetables fruits exhibits many biological properties for possible medical clinical applications such as its anti-inflamatory antioxidant effects. Thus, present...

10.1021/np400691n article EN Journal of Natural Products 2013-11-18

The bark of Mimosa tenuiflora (Willd.) Poiret (Leguminosae family), popularly known as "jurema preta" in Brazil, is used by the population Contendas Sincorá (Bahia State, Brazil) for treatment coughs and wound healing. Thus, aim this study was to evaluate antinociceptive anti-inflammatory activities ethanol extract (EEMT) solvent soluble fractions (hexane—H, DCM—D, EtOAc—E BuOH—B) vivo. Additionally, we synthesized 5,7-dihidroxy-4'-methoxyflavanone (isosakuranetin) isolated compound...

10.1371/journal.pone.0150839 article EN cc-by PLoS ONE 2016-03-08

The 15-deoxy-Δ<sup>12,14</sup>-prostaglandin J<sub>2</sub> (15d-PGJ<sub>2</sub>) is an endogenous ligand of peroxisome proliferator-activated receptors γ (PPAR-γ) and now recognized as a potent anti-inflammatory mediator. However, information regarding the influence 15d-PGJ<sub>2</sub> on inflammatory pain still unknown. In this study, we evaluated effect upon hypernociception mechanisms involved in effect. We observed that intraplantar administration (30–300 ng/paw) inhibits mechanical...

10.1124/jpet.107.126045 article EN Journal of Pharmacology and Experimental Therapeutics 2007-10-10

The objective of this study was to assess the effects oral ingestion β-glucans isolated from Saccharomyces cereviseae on metabolic profile, expression gingival inflammatory markers and amount alveolar bone loss in diabetic rats with periodontal disease. Diabetes mellitus induced 48 Wistar by intraperitoneal injection streptozotocin (80 mg/kg). After confirming diabetes diagnosis, animals were treated (by gavage) for 28 days. On 14th day period, disease using a ligature protocol. reduced both...

10.1371/journal.pone.0134742 article EN cc-by PLoS ONE 2015-08-20

Abstract Gout arthritis (GA) is a painful inflammatory disease in response to monosodium urate (MSU) crystals the joints. 15deoxy-Δ 12,14 -prostaglandin J 2 (15d-PGJ ) natural activator of PPAR-γ with analgesic, anti-inflammatory, and pro-resolution properties. Thus, we aimed evaluate effect mechanisms action 15d-PGJ nanocapsules (NC) model GA mice, since reduction 33-fold dose has been reported. Mice were treated -loaded NC, inert free (without NC), or NC+ GW9662, inhibitor. We show that NC...

10.1038/s41598-018-32334-0 article EN cc-by Scientific Reports 2018-09-12

Background and Purpose Epoxyeicosatrienoic acids (EETs) other epoxy fatty (EpFA) are lipid mediators that rapidly inactivated by soluble epoxide hydrolase (sEH). Uncontrolled chronic inflammatory disorders fail to sufficiently activate endogenous regulatory pathways, including the production of specialized pro‐resolving (SPMs). Here, we addressed relationship between SPMs EET/sEH axis explored effects sEH inhibition on resolving macrophage phenotype. Experimental Approach Mice were treated...

10.1111/bph.16009 article EN British Journal of Pharmacology 2022-12-12

Abstract We have recently demonstrated that gonadal steroid hormones decrease formalin‐induced temporomandibular joint nociception in rats. Given the attenuation of inflammation is a potential mechanism underlying this antinociceptive effect, we evaluated effect on inflammation. Plasma extravasation, major sign acute inflammation, and neutrophil migration, an important event related to tissue injury, were evaluated. Formalin induced significantly lower plasma extravasation migration...

10.1016/j.ejpain.2011.06.007 article EN European Journal of Pain 2011-07-09

To verify whether the nanoencapsulation of 15d-PGJ(2) in poly(D,L-lactide-co-glycolide) (PLGA) nanocapsules (15d-PGJ(2)-NC) might potentialize its antinociceptive activity into rats' temporomandibular joint (TMJ).Transmission electron microscopy (TEM) and atomic force (AFM) were used to evaluate morphology suspension PLGA nanocapsules. Rats pretreated (15 min) with an intra-TMJ injection unloaded or 15d-PGJ(2)-NC at concentrations 10, 100 1000 pg followed by ipsilateral 1.5% formalin. The...

10.1016/j.lfs.2012.04.035 article EN publisher-specific-oa Life Sciences 2012-04-28
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