Valtteri Rinne

ORCID: 0000-0003-2703-9426
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About
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Research Areas
  • Veterinary Pharmacology and Anesthesia
  • Anesthesia and Sedative Agents
  • Antibiotics Pharmacokinetics and Efficacy
  • Sirtuins and Resveratrol in Medicine
  • Calcium signaling and nucleotide metabolism
  • Maternal Mental Health During Pregnancy and Postpartum
  • Pain Management and Opioid Use
  • Hormonal Regulation and Hypertension
  • Maternal and Perinatal Health Interventions
  • Pharmacology and Obesity Treatment
  • Veterinary Equine Medical Research
  • Drug-Induced Hepatotoxicity and Protection
  • Adrenal Hormones and Disorders
  • Pharmacogenetics and Drug Metabolism
  • Bariatric Surgery and Outcomes
  • Cholesterol and Lipid Metabolism
  • Prenatal Substance Exposure Effects
  • Malaria Research and Control
  • Pediatric Pain Management Techniques
  • Breastfeeding Practices and Influences
  • Gastrointestinal motility and disorders
  • Infectious Encephalopathies and Encephalitis
  • Maternal and fetal healthcare
  • Anesthesia and Pain Management
  • Pharmacological Effects and Assays

Machida Endoscope (Japan)
2019-2023

Turku University Hospital
2016

University of Turku
2013-2016

University of Eastern Finland
2007-2008

Low 25-hydroxyvitamin D levels correlate with the prevalence of diabetes; however, mechanisms remain uncertain. Here, we show that nutritional deprivation–responsive regulate vitamin metabolism. Both fasting and diabetes suppressed hepatic cytochrome P450 (CYP) 2R1, main 25-hydroxylase responsible for first bioactivation step. Overexpression coactivator peroxisome proliferator–activated receptor γ 1-α (PGC-1α), induced physiologically by pathologically in diabetes, resulted dramatic...

10.2337/db18-1050 article EN Diabetes 2019-03-04

A new inhibitor for human sirtuin type proteins 1 and 2 (SIRT1 SIRT2) was discovered through virtual database screening in search of scaffolds. series compounds synthesized based on the hit compound (3-[[3-(4-tert-butylphenyl)1,2,4-oxadiazole-5-carbonyl]amino]-1-[3-(trifluoromethyl)phenyl]thiourea). The most potent nearly as reference (6-chloro-2,3,4,9-tetrahydro-1H-carbazole-1-carboxamide).

10.1021/jm800639h article EN Journal of Medicinal Chemistry 2008-07-22

Growing evidence supports the use of (2<i>R-trans</i>)-<i>N</i>-(2-(1,3,4,7,12<i>b</i>-hexahydro-2′-oxo-spiro(2<i>H</i>-benzofuro(2,3-<i>a</i>)quinolizine-2,4′-imidazolidin)-3′-yl)ethyl) methanesulfonamide (MK-467), a peripherally acting α<sub>2</sub>-adrenoceptor antagonist, in conjunction with sedative-anesthetic agent dexmedetomidine animals to avoid hemodynamic compromise. We evaluated possible effects different doses MK-467 on plasma concentrations eight beagle dogs. Both drugs were...

10.1124/dmd.111.042671 article EN Drug Metabolism and Disposition 2011-11-23

Liver X receptors (LXRs) are expressed in placenta and may be associated with pre-eclampsia (PE). Oxysterols act as agonists for LXRs. We recently proposed a new blood pressure-regulating circuit oxysterol 4β-hydroxycholesterol (4βHC) acting hypotensive factor via This study investigated the association between maternal plasma 4βHC, pressure (BP) indices, placental expression of LXR target genes, patient characteristics using data from Finnish Genetics Pre-Eclampsia Consortium (FINNPEC)...

10.1080/07853890.2025.2495763 article EN cc-by Annals of Medicine 2025-04-29

We investigated the influence of peripherally acting α2 -adrenoceptor antagonist MK-467 on sedative and antinociceptive actions plasma drug concentrations medetomidine, an agonist that is used in veterinary medicine as a analgesic agent. Eight healthy beagle dogs received intravenous medetomidine (10 μg/kg) or with (250 randomized crossover design. A standardized nociceptive pressure stimulus was applied to nail bed hindlimb. Times for withdrawal limb head lift were measured, sedation...

10.1111/jvp.12292 article EN Journal of Veterinary Pharmacology and Therapeutics 2016-01-14

ObjectiveTo study the effects of oromucosal detomidine gel administered sublingually to calves prior disbudding, and compare its efficacy with intravenously (IV) detomidine.Study designRandomised, prospective clinical study.AnimalsTwenty dairy aged 12.4 ± 4.4days (mean SD), weight 50.5 9.0 kg.MethodsDetomidine at 80 μg kg−1 was ten (GEL) 30 control IV (V. jugularis). Meloxicam (0.5 mg kg−1) local anaesthetic (lidocaine 3 were before heat cauterization horn buds. Heart rate (HR), body...

10.1111/vaa.12150 article EN cc-by-nc-nd Veterinary Anaesthesia and Analgesia 2014-03-14

Both effective analgesia and early breastfeeding play an important role in maternal neonatal well-being after Caesarean delivery. We studied controlled-release oxycodone tablet treatment for postoperative pain management determined the excretion of into breast milk.

10.1111/bcp.16008 article EN cc-by-nc British Journal of Clinical Pharmacology 2024-02-02

Regardless of progress in treatment coronary artery disease (CAD), there is still a significant residual risk death patients with CAD, highlighting the need for additional stratification markers. Our previous study provided evidence novel blood pressure-regulating mechanism involving 4β-hydroxycholesterol (4βHC), an agonist liver X receptors, as hypotensive factor. The aim was to determine role 4βHC prognostic factor CAD.

10.1161/jaha.123.031824 article EN cc-by-nc-nd Journal of the American Heart Association 2024-02-23

Abstract Oxycodone is an opioid analgesic with several pharmacologically active metabolites and relatively narrow therapeutic index. Cytochrome P450 (CYP) 3A4 CYP2D6 play major roles in the metabolism of oxycodone its metabolites. Thus, inhibition induction these enzymes may result substantial changes exposure both In this study, a physiologically based pharmacokinetic (PBPK) model was built using GastroPlus™ software for oxycodone, two primary (noroxycodone, oxymorphone) one secondary...

10.1002/bdd.2215 article EN Biopharmaceutics & Drug Disposition 2020-01-11

While a drug treatment is unavailable, the global incidence of Dengue virus (DENV) infections and its associated severe manifestations continues to rise. We report construction first physiologically based pharmacokinetic/pharmacodynamic (PBPK/PD) model that predicts viremia levels in relevant target organs on preclinical data with broad spectrum antiviral soraphen A (SorA), an inhibitor host cell acetyl-CoA-carboxylase. SorA was highly effective against DENV vitro (EC50 = 4.7 nM) showed vivo...

10.1021/acsptsci.1c00078 article EN ACS Pharmacology & Translational Science 2021-08-30

Cardiac bypass surgery patients have early postoperative interventions that elicit breakthrough pain. We evaluated the use of intranasal fentanyl for pain management in these patients. Multimodal analgesia (paracetamol 1 g three times a day, oxycodone 2–3 mg boluses with patient-controlled intravenous pump) was used 16 (age 49–70 years, weight 59–129 kg) after cardiac surgery. Intranasal 100 µg or 200 to manage on first and third mornings randomised order. Blood samples were collected up 3 h...

10.1007/s40262-021-01002-4 article EN cc-by-nc Clinical Pharmacokinetics 2021-03-09

Opioids are used for pain relief during the first stage of labor. Oxycodone can cause maternal hypotension that may modify utero- and fetoplacental circulatory physiology. We hypothesized intravenous (i.v.) oxycodone has no detrimental effect on hemodynamics early labor.Twenty-two parturients requiring labor were randomized in a double-blinded placebo-controlled study. By Doppler ultrasonography, both uterine artery (Ut) umbilical vein (UV) volume blood flows (Q), Ut pulsatility index (PI),...

10.1111/aogs.14603 article EN cc-by-nc-nd Acta Obstetricia Et Gynecologica Scandinavica 2023-06-21

The pharmacokinetic profile of fat-soluble vitamins A, E, K1, and D3 co-administered with liquid paraffin or water in an experimental rat model was investigated. Animals received a solution the four orally through probe, followed 10 minutes later by administration either product dissolved (Emuliquen Simple®) (control). Vitamin formulations were 20, 50, 0.30 0.10 mg/kg for D3, respectively. Blood samples collected before dosing at 0.17, 1, 2, 4, 8, 24 hours post-dosing. concentrations...

10.20944/preprints202309.2096.v1 preprint EN 2023-09-29
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