S1506 Search Results


93
New England Biolabs rack neb
Rack Neb, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 93 stars, based on 1 article reviews
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93
Selleck Chemicals perindopril erbumine
Pharmacological inhibition of ACE or AT1-R attenuates METH-induced hyperlocomotion. (A) METH induced hyperlocomotion in mice. (B) <t>Perindopril,</t> an ACE inhibitor, attenuated METH-induced behavioral sensitization. *p < 0.05, **p < 0.01, vehicle-saline group n = 11, vehicle-METH group n = 10, perindopril-METH group n = 14, perindopril-saline group n = 12. (C) Ang II expression, as measured by ELISA, was downregulated by perindopril in METH-treated mice. *p < 0.05, ***p < 0.001, n = 4 for each group. (D) Telmisartan, an AT1-R antagonist, attenuated METH-induced hyperlocomotion in mice. *p < 0.05, **p < 0.01, vehicle-saline group, vehicle-METH group, telmisartan-METH group n = 12 for each group, telmisartan-saline group n = 10. (E) Losartan, an AT1-R antagonist, showed no effect on METH-induced hyperlocomotion. Vehicle-saline group, n = 12; vehicle-METH group, n = 12; losartan-METH group, n = 13; losartan-saline group, n = 11
Perindopril Erbumine, supplied by Selleck Chemicals, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 93 stars, based on 1 article reviews
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90
Beyotime actinomycin d s1506
Pharmacological inhibition of ACE or AT1-R attenuates METH-induced hyperlocomotion. (A) METH induced hyperlocomotion in mice. (B) <t>Perindopril,</t> an ACE inhibitor, attenuated METH-induced behavioral sensitization. *p < 0.05, **p < 0.01, vehicle-saline group n = 11, vehicle-METH group n = 10, perindopril-METH group n = 14, perindopril-saline group n = 12. (C) Ang II expression, as measured by ELISA, was downregulated by perindopril in METH-treated mice. *p < 0.05, ***p < 0.001, n = 4 for each group. (D) Telmisartan, an AT1-R antagonist, attenuated METH-induced hyperlocomotion in mice. *p < 0.05, **p < 0.01, vehicle-saline group, vehicle-METH group, telmisartan-METH group n = 12 for each group, telmisartan-saline group n = 10. (E) Losartan, an AT1-R antagonist, showed no effect on METH-induced hyperlocomotion. Vehicle-saline group, n = 12; vehicle-METH group, n = 12; losartan-METH group, n = 13; losartan-saline group, n = 11
Actinomycin D S1506, supplied by Beyotime, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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Image Search Results


Pharmacological inhibition of ACE or AT1-R attenuates METH-induced hyperlocomotion. (A) METH induced hyperlocomotion in mice. (B) Perindopril, an ACE inhibitor, attenuated METH-induced behavioral sensitization. *p < 0.05, **p < 0.01, vehicle-saline group n = 11, vehicle-METH group n = 10, perindopril-METH group n = 14, perindopril-saline group n = 12. (C) Ang II expression, as measured by ELISA, was downregulated by perindopril in METH-treated mice. *p < 0.05, ***p < 0.001, n = 4 for each group. (D) Telmisartan, an AT1-R antagonist, attenuated METH-induced hyperlocomotion in mice. *p < 0.05, **p < 0.01, vehicle-saline group, vehicle-METH group, telmisartan-METH group n = 12 for each group, telmisartan-saline group n = 10. (E) Losartan, an AT1-R antagonist, showed no effect on METH-induced hyperlocomotion. Vehicle-saline group, n = 12; vehicle-METH group, n = 12; losartan-METH group, n = 13; losartan-saline group, n = 11

Journal: Neurotherapeutics

Article Title: Brain Renin–Angiotensin System Blockade Attenuates Methamphetamine-Induced Hyperlocomotion and Neurotoxicity

doi: 10.1007/s13311-018-0613-8

Figure Lengend Snippet: Pharmacological inhibition of ACE or AT1-R attenuates METH-induced hyperlocomotion. (A) METH induced hyperlocomotion in mice. (B) Perindopril, an ACE inhibitor, attenuated METH-induced behavioral sensitization. *p < 0.05, **p < 0.01, vehicle-saline group n = 11, vehicle-METH group n = 10, perindopril-METH group n = 14, perindopril-saline group n = 12. (C) Ang II expression, as measured by ELISA, was downregulated by perindopril in METH-treated mice. *p < 0.05, ***p < 0.001, n = 4 for each group. (D) Telmisartan, an AT1-R antagonist, attenuated METH-induced hyperlocomotion in mice. *p < 0.05, **p < 0.01, vehicle-saline group, vehicle-METH group, telmisartan-METH group n = 12 for each group, telmisartan-saline group n = 10. (E) Losartan, an AT1-R antagonist, showed no effect on METH-induced hyperlocomotion. Vehicle-saline group, n = 12; vehicle-METH group, n = 12; losartan-METH group, n = 13; losartan-saline group, n = 11

Article Snippet: Perindopril erbumine, telmisartan, and losartan potassium were purchased from Selleck Chemicals (Houston, TX).

Techniques: Inhibition, Saline, Expressing, Enzyme-linked Immunosorbent Assay