Nicotine is a component of tobacco products and is one of the most commonly abused substances that leads to addiction. Therefore, the present study was performed to investigate the behavioral pattern and toxicity by nicotine exposure in planarians. Basically, planarians were exposed to different concentration of nicotine for 5 min. To investigate detoxification effect, planarians were exposed to nicotine for 5 min, and treated glycyrrhizin for 5 min, then motility and seizure-like behavior were observed for 5 min. As a result, the motility of nicotine-exposed planarians decreased approximately more than 50% compared to freshwater control. However, the motility of glycyrrhizin-exposed planarians recovered than nicotineexposed planarians. In the assessment of seizure-like behavioral pattern, planarians exposed to nicotine showed head-bop or c-like type rather than screw-like or snake-like patterns. However, planarians exposed to glycyrrhizin showed no seizure-like behavior. To examine the oxidative stress response, planarians were cultured in fresh water containing 1 mM nicotine for 1 day. Planarians were homogenized and extracted to assay the contents of reactive oxygen species (ROS), lipid hydroperoxides (LH), glutathione (GSH), catalase (CAT), and superoxide dismutase (SOD). The result showed that a significantly higher level of ROS, LH indicated in planarians exposed to nicotine, on the other hand, glycyrrhizin-exposed planarians were significantly decreased ROS, LH levels. In conclusion, the motility decreased when planarians were exposed to nicotine, in a dose-dependent manner, whereas seizurelike behavior increased. Nicotine induced behavioral disturbances and cell toxicity in planarians were recovered by glycyrrhizin, suggesting a candidate substance for nicotine addiction treatment.

Nicotine of tobacco component has a controversial impact in the clinical outcome of dental implants. Although numerous nicotine effects on bone healing around implants have been presented, it is rarely reported in vitro study about normal human osteoblast(NHost) from oral and maxillofacial area at the surface of implants. The purpose of the present study was to evaluate the effect of nicotine on the proliferation and differentiation response of NHost to plasmatic and salivary levels of nicotine reported in smokers at the surface of screw-type plasma-sprayed titanium implants. NHosts were seeded on the surface of titanium implants and cultured for 21 days in α-MEM supplemented with 10% FBS, 50mg/ml ascorbic acid, 5mM β-glycerophosphate and 100nM dexamethasone. Seeded implants were exposed to various nicotine concentration(0.05-0.5mg/ml) from 1 to 21 days, and characterized for cell morphology, proliferation, differentiation, alkaline phosphatase(ALP) activity and ionized calcium concentration(Cai) of medium. Continuous exposure to higher nicotine concentration(above 0.3mg/ml) induced a dose- and time-dependent vacuolation of the cytoplasm, and a tendency to detach from the implant surface. 0.05mg/ml(lower nicotine concentration) did not cause significant effects in the cell proliferation and ALP activity. 0.1-0.2mg/ml caused evident dose-dependent effects in increased cell proliferation, ALP activity and earlier onset of matrix mineralization at levels up to 0.2mg/ml, while a dose-dependent inhibitory effect at 0.3-0.5mg/ml. Cai concentration of control group was decreased at 14 days. Increased Cai concentration at 0.1-0.2mg/ml, decreased Cai concentration at 0.3mg/ml and no change at 0.5mg/ml during the culture period were seen. It suggested that nicotine concentration could paly an role in modulating NHost activity as a contributing factor associated with proliferation and differentiation of NHost at the surface of implants.

본 연구에서는 nicotine 분해에 효과에 대하여 해양식물 유래의 후코이단을 이용하여 시험관에서 직접 혼합법 및 세포주 시험에서 nicotine의 cotinine으로의 전환능을 측정하였다. 직접 혼합법 시험결과, 후코이단 1 μg/mL에서 시간이 경과함에 따라서 nicotine의 cotinine으로의 전환 정도가 대조군 대비 증가하여 시험 종료 시점에서 15배의 증가율을 나타내었다. 세포주을 이용한 nicotine의 분해능 시험 결과, 시험 종료 시점에서 대조군 대비 6배의 cotinine 증가율을 나타내었다. 양성 대조군으로 사용한 녹차 추출물 대비 nicotine 분해능은 우수한 것으로 평가되었다. 그러나 후코이단의 항산화능은 녹차 추출물과 대비하여 낮았으며, 항산화 주요 기능을 갖는 폴리페놀 및 플라보노이드 성분 역시 낮았다. 본 시험 결과가 나타내는 바는 후코이단의 nicotine의 cotinine으로의 전환능에 대한 입증을 하였으며 이는 금연 보조 역할을 할 수 있는 기능성 소재로 사료된다.

This study investigated the effect of smoking on Indoor Air Quality in smoking allowed buildings. Total 26 buildings(Restaurants 3, Billiards 4, Karaokes 6, Golfs 7, Pubs 6) were surveyed for nicotine, PM₁₀, CO₂, CO, NO₂, HCHO, TVOCs, benzene, toluene, ethylbenzene, styrene and xylene at quiet and busy time, respectively. The concentrations of nicotine, PM₁₀, CO₂ and benzene were significantly higher(p<0.05) at busy time compared to the quiet time. Some buildings exceeded Indoor Air Quality Standards for PM₁₀, CO₂, HCHO and TVOCs. Our results show that smoking-ban legistration should be introduced to improve Indoor Air Quality.

Exposure to environmental tobacco smoke (ETS) could adversely affect health. The aim of this study was to quantify the contribution of ETS exposure in nonsmokers of entertainment facilities. We simultaneously measured nicotine and nitrogen dioxide (NO₂), which are known as indicators of ETS, concentrations in indoor internet cafe, billiard, karaoke, bar and restaurant, and estimated exposure level of other harmful agents occurred from tobacco smoking. Mean nicotine concentration (10.57±2.53㎍ /m³ ) of internet cafe was the highest comparing to other facilities, whereas mean concentration of restaurant where was non-smoking area was 0.28±0.08㎍ /m³ . There was statistically not correlated between NO₂ and nicotine concentrations in entertainment facilities. Therefore, the use of NO₂ concentration as indicator of ETS exposure may not be available. To date, there are no standards about each agent occurred from ETS. Consequently administrative control and regulation, and further researches in relation to ETS exposure should be needed.

In vivo nicotine is associated with Alzheimer's, Parkinson's and lung cancer. Diagnostic assays of these diseases depend on very low analytical detection limits. In this study, a sensitive analytical method was examined using a voltammetric graphite pencil electrode (GPE) and a modified carbon nanotube paste electrode (CNE). The optimum analytical conditions for both electrodes were compared using square wave anodic stripping voltammetry (SW) and cyclic voltammetry (CV) obtaining 400 sec accumulation time and oxidation peak. Under optimum parameters, the stripping working range of GPE was 5.0-40.0μg/L, CNE: 0.1-0.8 and 5-50μg/L. Quantification limits were 5.0μg/L for GPE and 0.1μg/L for CNE, while detection limits were 0.6μg/L for GPE and 0.07μg/L for CNE. A standard deviation of 10.0μg/L was observed for 0.064 GPE and 0.095 CNE (n = 12) using 400 sec accumulation time. The results obtained can be applied to non.treated urine and ex vivo biological diagnostics.

Nicotine, a major teratogen of cigarettes smoke induces embryonic abnormalities during the early stages of organogenesis. In this study, the protective effect of β-carotene against nicotine–induced embryos was evaluated by morphologic scoring, nile blue staining, lipid peroxidation, SOD activity assay and real-time PCR. The embryos exposed to nicotine (1 μM) revealed remarkable morphological anomalies compared to normal control group (p<0.05), but when β-carotene (1×10‒4 μM or 5×10‒4 μM) was added concurrently to the embryos exposed to nicotine, morphological parameters were significantly improved (p<0.05). Nicotine induced oxidative stress by increased lipid peroxidation, expression of proinflammatory cytokines (TNF-α and IL-1β), caspases-3 and decreased SOD activity. However, administration of β-carotene (1×10‒4 μM or 5×10‒4 μM) restored the SOD level and decreased oxidative damage in the embryos. These results indicate that β-carotene effectively counteracts the deleterious effects of nicotine on embryos and attenuates oxidative damage possibly through its antioxidant effects.

Nicotine, a major toxic component in tobacco smoke, leads to severe embryonic damages on organogenesis. We investigated if resveratrol can inhibit the nicotine–induced teratogenesis in the cultured mouse embryos (embryonic day 8.5) for 48 hours using a whole embryo culture system. The embryos exposed to nicotine (1 μM) revealed severe morphological anomalies, the increased levels of caspase-3 mRNA and lipid peroxidation, and further the lowered levels of mitochondrial manganese superoxide dismutase (SOD), cytosolic glutathione peroxidase (GPx), phospholipid hydroperoxide GPx, hypoxia-inducible factor 1α, and sirtuin mRNAs and SOD activity significantly compared to normal control group (p<0.05). However, whenre sveratrol(1×10‒5 μMor1 ×10‒4 μM) was added concurrently to the embryos exposed to nicotine, these all parameters were significantly improved (p<0.05).These findings indicate that resveratrol has a protective effect against nicotine-induced teratogenesis in mouse embryos throughout antioxidative and anti-apoptotic activities.

Human β- defensin-2 (hBD-2) is an antimicrobial peptide which is produced by epithelial cells after stimulation with microorganisms or inflammatory mediators. However, little is known as to whether the LPS and nicotine induces the expression of hBD-2 in periodontal l igament (PDL) cells. T he p urpose o f this s tudy was t o investigate t he r oles o f MAPKs pathway o f nicotine a nd L PS-induced hBD-2 expression in PDL cells. The maximal expression of hBD-2 was observed in nicotine 5 mM and LPS 1 μg/ml treated PDL cells. Nicotine and LPS induced the phosphorylation of p38, c-Jun N-terminal kinase 1 and 2 (JNK1/2), and extracellular signal-regulated kinases 1 and 2 (ERK1/2) MAPK. ERK1/2 inhibitor SB203580, p38 inhibitor PD98059, and JNK inhibitor SP600125, blocked the effects of nicotine and LPS on hBD-2 upregulation in PDL cells. These results collectively suggest that hBD-2 is up-regulated in nicotine and LPS-treated PDL cells through activation of p38, ERK and JNK MAPKs pathway. Our data regarding the up-regulation of hBD-2 may help us to understand the antimicrobial mechanism in periodontal disease

Heme oxygenase-l (HO-l) exhibits cyt oprotective effects in many different cell types and is induced by nicotine exposure in human gingival fibroblasts‘ However‘ therole of HO- l in cancer cells exposed to nicotine has not previously been descnbed We investigated the effects of nicotine on HO-l protein expression and cell viability in immortalized (IHOK) and malignant (HN12) human ora l keratinocyte cells using the MTT assay and Western blotting. We al so examined the involvement of t he phosphoinosit ide-3-0H- kinase (PI3K), mitogen-acti vated protein kinase (MAPK) , and nucJear factor-κ B (NF-κ B) signaling pathways in nicotine-induced cytotoxicity and HO- l levels in IHOK and HN12 cell s‘ Nicotine induced HO- l pro ducti on and had cytotoxic effects on cells in both a concentration- and time-dependent manner. Nicotine-induced cytotox icity and accumulation of HO- l were greater in JJ-IOK cells than in HN12 cells Molecular inhibitors of the ERK, p38 MAP kinase, PI3K, and NF-κ B signaling pathways blocked the cytotoxic effects and induction of J-IO-l expression by nicotine. Treatmen t with an t ioxida nts (bil irubin, N-acetyl cysteine) protected cells against nicotine-induced cytotoxicity and blocked the upregula tion of J-IO- l, the effects of which were more pronounced in II-IOK cells than in HN12 cells Collecti vely, these results suggest that J-IO- l plays a principal role in the protective response to nicotine in oral cancel and immortalized keratinocytes. Moreover, the addition of exogenous antioxidants may help to protect oral epithelial cells as chemopreventive agents against nicotine-induced oxidative stress.

Heme oxygenase-l (HO-l) exhibits cyt oprotective effects in many different cell types and is induced by nicotine exposure in human gingival fibroblasts‘ However‘ therole of HO- l in cancer cells exposed to nicotine has not previously been descnbed We investigated the effects of nicotine on HO-l protein expression and cell viability in immortalized (IHOK) and malignant (HN12) human ora l keratinocyte cells using the MTT assay and Western blotting. We al so examined the involvement of t he phosphoinosit ide-3-0H- kinase (PI3K), mitogen-acti vated protein kinase (MAPK) , and nucJear factor-κ B (NF-κ B) signaling pathways in nicotine-induced cytotoxicity and HO- l levels in IHOK and HN12 cell s‘ Nicotine induced HO- l pro ducti on and had cytotoxic effects on cells in both a concentration- and time-dependent manner. Nicotine-induced cytotox icity and accumulation of HO- l were greater in JJ-IOK cells than in HN12 cells Molecular inhibitors of the ERK, p38 MAP kinase, PI3K, and NF-κ B signaling pathways blocked the cytotoxic effects and induction of J-IO-l expression by nicotine. Treatmen t with an t ioxida nts (bil irubin, N-acetyl cysteine) protected cells against nicotine-induced cytotoxicity and blocked the upregula tion of J-IO- l, the effects of which were more pronounced in II-IOK cells than in HN12 cells Collecti vely, these results suggest that J-IO- l plays a principal role in the protective response to nicotine in oral cancel and immortalized keratinocytes. Moreover, the addition of exogenous antioxidants may help to protect oral epithelial cells as chemopreventive agents against nicotine-induced oxidative stress.

본 연구는 BPA 및 nicotine 첨가 농도와 배양 시간이 돼지 난자의 체외성숙에 미치는 영향을 조사하였다. BPA와 nicotine이 첨가된 TCM-199배양액에서 시간 난자를 배양했을 때 체외성 숙율을 조사하였다. BPA농도가 높을수록 체외성숙율이 유의적으로 낮게 나타났다. BPA를 첨가한 TCM-199 배양액에서 난자를 44시간 배양했을 때 체외성숙율은 각각 로서 첨가 농도가 증가할수록 낮은 체외성숙율을 나타냈다. 난자를 nicotine를 첨가

Nicotine(2~15mg/kg 2주간, 100mg/kg 회 투여)을 생후 4개월령 수컷 생쥐에 투여한 후, 고환에 미치는 광학현미경적 소견은 다음과 같다. 1. Nicotine 2mg/kg 투여군에서는 정세관과 정세관 주위의 Leydig 세포도 핵과 세포질이 뚜렷한 정상적인 소견을 나타내었으나, 5 mg/kg 투여군에서는 Leydig 세포의 핵과 세포질이 다소 비후되었으며, 염색정도가 약하였다. 2. 10 mg/kg 투여군은 대부분 정세관내의 정자발

The PC game rooms in Korea have a problem in the aspect of indoor air quality because there are many occupants for 24 hours where the smoking is allowed. This study was carried out to evaluate indoor air quality (IAQ) including the size distribution of respirable suspended particulates (RSP) and airborne nicotine concentration in selected PC game rooms. The subjects are 6 PC game rooms in Seoul and Sung-Nam Cities. In this study, airborne RSP and nicotine concentrations were measured during a period from February to March, 2003. Significant correlation has been found between the concentrations of RSP and nicotine in PC game room. Also the negative correlation was found between room area and number of operating fan. The correlation coefficients between RSP size distribution and nicotine concentration were 0.868, 0.866, 0.870 in the stages 2 (cut-point 14.80㎛), 5 (cut-point 3.50㎛), and 8 (cut-point 0.52㎛) from Marple's 8-stage cascade impactor, respectively. In conclusion, RSP concentration in PC game room has a tendency to increase by smoking. Therefore, it is suggested that the effective air control system and education program be applied for PC game room.

천연식물소재 및 한약재 추출제재인 식물추출 혼합제재가 인체내에서 니코틴 분해능에 미치는 영향을 FRCFR5 세포주, Xenopus oocyte, 임상 실험을 통하여 검토하였다. 본 실험은 체내에 잔존하는 니코틴이 식물추출 혼합 제재에 의해 무독한 대사산물인 코티닌으로 분해량이 증가되고 동시에 NNK, NNN, NNA 등과 같은 폐암 유발물질인 니트로사민 유도체 생성 경로가 억제될 것이라는 가정을 전제로 실험을 수행하였다. 본 실험 결과에서 볼 수 있듯이 식물추출 혼합 제재에는 니코틴에서 코티닌으로 전환시키는 대사 활성물질이 함유되어 있다는 사실을 알 수 있으나, 실제로 어떤 유효성분들이 관여하는지 그리고 정확한 작용 기작을 규명하기 위해서는 더 많은 분석 및 생화학적 연구가 앞으로수행되어야 할 것이다. 간세포에서 유래된 FRCFR5 세포주 실험 결과, 니코틴과 식물추출 혼합 제재가 첨가된 배지에서 니코틴과 물을 첨가한 배지보다 니코틴에서 코티닌으로 전환능력이 약 2∼3배 높게 나타났으며, 이러한 결과는 Xenopus oocyte에 직접 주사한 경우와 거의 비슷한 양상을 보였다. 임상실험 결과 식물추출 혼합 제재 음료를 음용하고 담배를 피운 실험군이 물을 음용하고 담배를 피운 대조군에 비해 약 2배 정도 높은 코티닌 함량을 나타내었다. 이는 실험군의 소변 중에 계속적으로 다량의 코티닌이 배출되는 것을 의미하며, 식물추출 혼합 제재 섭취시 체내에 존재하는 니코틴이 코티닌으로 지속적이면서 효과적으로 전환되는 것을 말한다. 이상의 생체 내·외 실험에서 알 수 있듯이 식물추출혼합물은 니코틴에서 코티닌 생성을 약 2배정도 증가 시키는 것을 알 수 있었다.

담배나방(Heliocoverpa assulta)와 파밤나방(Spodoptera exigua)유충에 대한 유기인계 살충제인 다이아지논과 담배의 산물인 니코틴의 영향을 조사하기 위하여 본 실험을 시행하였다. 다이아지논이 처리된 담배나방유충의 사망률은 파밤나방유충의 경우보다 훨씬 높았으며 니코틴 처리구에서는 이와 반대양상을 나타내었다. 담배나방유충 중장의 cytochrome P-450 monooxygenases (MFO) 활성은 다이아지논 처리구에 비해서 니코틴 처리구에서 더욱 높게 나타났다. 담배나방유충을 기주식물인 담배잎으로 사육하였을 때 다른 화합물과는 달리 대부분의 니코틴은 변화 없이 배설되었다.

Nicotine is a major component of tobacco alkaloids. Nicotine is synthesized via putrescine N-methyl transferase (PMT), quinolinate phosphoribosyl transferase (QPT) and nicotine synthase. In this study, we down regulated the QPT activity using RNAi technique. RNAi vector was constructed by amplifying 500 bp region of QPT and inserted to pFGJJ374 vector in forward and reverse directions. We transferred the vector to Agrobacterium tumefaciens (LBA4404) and transformed Nicotiana tabacum (NC82). The nicotine contents of the transformant were significantly decreased by the transformation. The QPT gene expression of the transformant was decreased to 1/40 - 1/218 of the control from the quantitative RT-PCR. We made homogeneous transformed lines by segregation of the transformants. The low nicotine contents of the homogeneous lines were steadily maintained over the generations. The transformed lines could be used for low nicotine cigarette manufacturing.